IQVIA

Team  IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. With direct access to the world’s most comprehensive healthcare information, analytics and research resources, IQVIA Real World Solutions (RWS) experts design and deliver innovative data– and technology-enabled evidence programs to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients.      Within the RWS group, the IQVIA Europe, Middle East, Africa (EMEA) Real World Methods and Evidence Generation (RW MEG) team is composed of around 90 highly qualified multi-disciplinary professionals from a variety of disciplines including health economics, statistics, epidemiology and data management, located across 8 geographies.     Our clients operate in the life sciences industry, including the global top 20 pharmaceutical companies, medical device and biotech companies, as well as public health providers and regulatory authorities. Our clients look for insight and evidence on the safety, efficacy, effectiveness and cost-effectiveness of health care delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people.      For more information about our company please visit our website: https://www.iqvia.com     Role overview  In this role within the EMEA RW MEG you will be producing materials and services relating to the Health Economics Outcomes Research business areas (health economic modelling, evidence synthesis, statistical analysis, health technology assessment submissions, report and publication development for value communication) that generate value for our clients. The role of the Consultant is expected to play an important role in shaping the team’s literature review offerings.   The successful candidate:  Will be involved in shaping and leading the team and offerings, working closely with the EMEA RWS Center of Excellence for Systematic Literature Review and the wider senior leadership team  Has a good understanding of systematic literature methods (e.g., Cochrane)  Can independently develop searches in various databases (e.g., EMBASE, MEDLINE, Cochrane, PubMed, etc.) and proficient in using OVID SP or another similar platform  Keeps up to date on new methodologies and HTAs requirements for systematic literature reviews and be an in-house go-to expert for the team  Has a good understand of different types of literature reviews (e.g., systematic, targeted, pragmatic, etc.)  Manages literature review projects with senior oversight  Guides the team on interpretation/qualitative synthesis of the literature review findings   Oversees literature review projects that meet rigorous HTA requirements, conducts quality control of literature review deliverables (searches, screening files, extractions, reporting)  Is a day-to-day contact with clients who will include pharmaceutical, biotechnology and medical devices companies with global and regional headquarters based in the EMEA region, and occasionally their affiliate teams, with senior oversight  Oversees the development of research questions, PICOS criteria, search strategies and literature review protocols   Contributes to business development as well as internal initiatives for the advancement of innovative methodological approaches   Collaborates with other business areas and functions of the organisation to deliver client services and support the development of new offerings  Qualifications and desired experience We are looking for a candidate with a good mix of academic and professional experience, domain experience and interpersonal skills. An ideal candidate has a good knowledge of literature review methods and has experience in conducting rigorous literature reviews in health sciences. The ideal candidate will also have a good understanding of the typical structure of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve client’s aims.   The list below should be viewed as a guide rather than a checklist. We want to prioritise recruiting candidates who will incorporate IQVIA’s value of ‘brave minds’ with their previous experience to put a personal spin on this role. If you share our passion for driving healthcare advancements through unparalleled data and have a passion for collaboration and solving complex problems, we encourage interested candidates who feel like they could be a good fit for the role to apply.  Desired skills and qualifications:   Postgraduate degree level education or higher from a relevant discipline such as health or bioscience-related, medicine, biomedical sciences, health economics, health policy, epidemiology, public health, or information science  Prior relevant experience, >2 years (such as, but not limited to experience in systematic literature reviews and/or meta-analyses)  Understanding of research principles, PRISMA principles, Cochrane guideline for SLRs, methods of the assessment of risk of bias for different study designs  Understanding of the principles of evidence-based healthcare, critical appraisal and the interpretation and synthesis of health care research   Understanding (and experience is advantageous) with the HTA agency requirements for evidence reviews and synthesis  Excellent oral and written communication skills  Accuracy, attention to detail and time management skills  An understanding of meta-analysis methods is advantageous, but not essential  Strong written and verbal communication skills with fluency in English  Demonstrable commercial awareness and thorough understanding of the pharmaceutical industry is advantageous   Proficiency in MS Word, PowerPoint, Excel  Eligibility to work in one of our office locations without visa sponsorship   Please submit your  CV in English. Our commitment to youIQVIA are committed to your professional growth in the healthcare industry. You will join a team of 90+ professionals working as subject matter experts, representing multiple disciplines, including HTA, health economic modelling, evidence synthesis, literature reviews, epidemiology, biostatistics, and data management. During the first three months new joiners will be paired with a more experienced hire in our ‘buddy’ system to offer support and advice in an informal setting.  IQVIA offers numerous training opportunities. You will have opportunities for external trainings and conference attendance aligned with business and team objectives. IQVIA also offers unlimited access to eLearning courses on LinkedIn Learning and Learning Edge as well as access to our internal training courses.  You will be rewarded with a competitive salary, bonus, and benefits. You will have the opportunity to gain invaluable and transferable experience within an innovative team spread out across the EMEA region. Your new role offers flexibility, including remote working and occasional office visits.  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Associate Clinical Trials Regulatory Manager EMEA Homebased Job Summary The Associate Clinical Trials Regulatory Manager provides regulatory support and oversight for clinical trial submissions across global programs. This role is responsible for preparing and reviewing regulatory documentation, managing submissions, ensuring regulatory compliance, and supporting clients and internal stakeholders throughout the clinical trial lifecycle. This is not a people manager role, but a process management position. Key Responsibilities Serve as the Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects and programs. Provide regulatory oversight and strategic guidance to internal and external stakeholders. Review scientific and regulatory documentation, conduct gap analyses, and provide recommendations. Author and/or review key regulatory documents, including Investigational Medicinal Product Dossiers (IMPDs) and clinical trial justifications. Coordinate and support European centralized submissions and global country submissions. Ensure project deliverables are completed on time, within scope, and in compliance with regulatory requirements. Maintain accurate records in internal systems, databases, and tracking tools in accordance with SOPs. Support business development activities by providing regulatory expertise. Deliver regulatory training and presentations as required. Mentor junior team members and contribute to departmental knowledge sharing initiatives. Qualifications and Experience Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs, or a related field. Typically 3–5 years of experience in Regulatory Affairs within the pharmaceutical, biotechnology, CRO, or clinical research industry. Experience supporting clinical trial submissions and regulatory documentation. Strong scientific writing, document review, project management, and stakeholder engagement skills. Advanced knowledge of clinical trial regulations and regulatory submission processes. Knowledge & Competencies Advanced knowledge of regulatory affairs and clinical trial submission requirements. Strong analytical and problem-solving skills. Excellent communication and collaboration abilities. Ability to work independently and manage multiple priorities in a fast-paced environment. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need. IQVIA Biotech has an exciting position within its EU Clinical Monitoring team. The Clinical Monitoring department is the largest team within IQVIA Biotech, providing CRA, Clinical Leads, Management and oversight to global clinical studies. Please note, for this role you must be based in the Netherlands. Basic Functions: Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites.  Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements. Responsibilities Participates in the investigator recruitment process, performing site evaluation visits of potential investigators to evaluate the capability of the site to successfully manage and conduct the clinical study. Coordinate activities with the site and internal departments in preparation for the initiation of the study. Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF and EDC system; monitoring activities and study close-out activities. Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS. Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs. Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor.  Performs investigational product inventory.  Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification and works with sites to resolve data queries and produce robust data. May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA. Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested. Assists with, and attends, Investigator Meetings for assigned studies. Attends study-related, company, departmental, and external meetings, as required. Ensures all study deliverables are completed per IQVIA Biotech and study timelines Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs. Serves as mentor for junior CRAs and those new to the company and/or study. KNOWLEDGE, SKILLS AND ABILITIES: Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology. Minimum of 1-2 years of onsite monitoring experience is a must. Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions. Able to form productive professional relationships both internally within own function, cross-functionally and externally with health care professionals. Able to handle several priorities within multiple, complex trials. Able to reason independently and recommend specific solutions in clinical settings. Able to work independently, prioritize, and work within a matrix team environment. Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research. Candidates must have strong communication levels of Dutch and English. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Our MedTech Healthcare Collection Associate will be responsible for collecting reprocessed medical equipment in a hospital. You will be working with surgical, non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. This is a great opportunity for you to gain medical experience!  You will have a flexible schedule Monday thru Friday - No evenings/No Weekends and an opportunity to grow and expand into new opportunities while earning supplemental income and learning about the medical device industry.  What you will be doing in the role:Visit assigned hospitals as required to collect products to be reprocessed Package and ship product to client manufacturing plant Document and log daily collections totals Notify the local Sales team of shipping supply needs Appropriate PPE is provided to all employees prior to the start of assignments. Per Diem and flexible availability Job Requirements:  An active and unrestricted driver license is required for this position  Minimum High School diploma or equivalent Reliable vehicle for transportation Must be comfortable with basic software programs and Microsoft operating system  Excellent customer service skills and strong attention to detail Ability to lift 30-50 lbs Ability to clear hospital vendor credentialing requirements, including proof of vaccination status, required Position may/will require up to date immunizations.  Travel Requirement:Travel locally for up to 2-3 hours to support customer needs.  Must have an active driver license and a personal vehicle to use for job related assignments Travel, and your time traveling is paid, as is mileage. Preferred Attributes:Experience in healthcare, general labor, warehouse or customer service, is beneficial for this position. Ability to work independently in customer settings with minimal supervision. IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities.  Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  *Please note: Due to the nature of this role, it is not eligible for Visa sponsorship. #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $25-$27 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Combineer je medische kennis en communicatieve skills als jr. medisch afgevaardigde en bouw sterke vertrouwensrelaties op met artsen in regio Kortrijk, Ieper, Veurne, Roeselare, Oostende. Wat houdt de job in? Klantenopvolging Huisartsen en specialisten bezoeken en een professionele vertrouwensrelatie met hen uitbouwenDe wetenschappelijke kennis assimileren en ze op een gestructureerde, duidelijke en overtuigende manier overbrengenAnalyse, planning Actieplannen opstellen om de vooropgestelde objectieven te bereikenDe feedback van je dokters verwerken en analyserenDeelnemen aan meetings (team meetings, seminaries, cycle meetings)De belangrijkste artsen in je doelgroep identificerenWat breng jij mee? Je beschikt over een Bachelor of Master diploma (in een wetenschappelijke of commerciële richting)Je bent positief ingesteld, enthousiast, leergierig, ondernemend, klantgericht en flexibel.Je beschikt over uitstekende communicatieve vaardigheden en staat open voor verandering.Je bent sales gedreven.Je beschikt over een rijbewijs B en woont in de regioWat hebben we jou te bieden? Contract onbepaalde duurCompetitief salaris afgestemd op jouw ervaringAantrekkelijk pakket aan extralegale voorwaarden (inclusief bedrijfswagen + laadkaart, groeps- en hospitalisatieverzekering, ..)Uitdagende functie met veel autonomieBegeleiding en opleiding#LI-SD1 #LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

For one of its customers IQVIA is looking to recruit a GP Engagement & Omnichannel Key Accountmanager (Women’s Health).  This national function combines field and office-based work and and plays a key part in strengthening engagement with General Practitioners (GPs)  Does this sound like the perfect fit for you? Read on! What does the job entail? Basically we are looking for a driven business developer with digital skills who wants to further expand the GP channel through a smart mix of personal contact and digital engagement. Someone who thrives on building connections, sees opportunities in a large target audience, and knows how to turn those opportunities into tangible results. You will: Be the SPOC for GPs: engaging via face-to-face interactions, virtual meetings, events and congressesActively build and maintain relationships with GPs across your regionDevelop and implement an omnichannel GP journey in collaboration with marketingIdentify, organize and follow up on GP-focussed events and congressesDrive hybrid engagement strategies, combining digital and physical touchpointsInitiate and execute marketing activities (online & offline) based on GP needsCollaborate closely with KAMs (e.g. Specialties / Gynaecology) to ensure a consistent approachContribute actively to the digital transformation of the GP channelProactively identify new opportunities and expand the GP network and potentialWhat do you bring to the table? Experience in GP visits and field-based rolesKnowledge of GP events and congress landscapeDigital native with a strong affinity for omnichannel engagementBlend of business development mindset and marketing acumenHands-on ability to execute digital journeysStrong communicator who easily builds connections with physicians and can confidently present to and engage groupsAutonomous, proactive and results-driven (“will to win”)Strong team player, collaborating across sales, marketing, and digital teamsLanguages: Dutch, English and French (good proficiency required)What do we have to offer you? Contract with IQVIA (outsourcing)Competitive salary based on your experienceAttractive benefits package (including a company car + fuel card, group and hospitalization insurance, etc.)Challenging role with a high degree of autonomyMentoring and trainingReady to make an impact? Apply today! Send your resume to [email protected] #LI-CES #LI-SD1 #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvides the client relationship to a mid-sized client or clients through relationships with executives and leaders in the client organization in a part of mid-sized market or part of a large region. Grows revenue by leveraging the full IQVIA offerings and identifying new business opportunities. Essential Functions Under direct supervision, assists the sales team in selling IQVIA products and services within assigned accounts or territory to achieve assigned revenue goal.Participate in sales/proposal presentations in face-to-face meetings with potential clients.Identifies contract expansion opportunities within assigned account(s) and elevates for qualification and decision to pursue.May interfaces with marketing, market research and/or IT at the user level in existing and prospective client(s).Represents the company to the client and the client to the company in all sales related activities.Monitors client satisfaction with contracted deliverables and provides feedback to Account team members on level of customer satisfaction.Effectively manage renewals and subscriptions.As required, may participate in contract renewal efforts on large multi-year contracts.Qualifications Bachelor's Degree  PrefFour (4) years experience Req preferrable in media and pharmaceutical industriesIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $54,300.00 - $135,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewUnder guidance, provides client relationship to a client or clients through relationships with managers in the client organization. Grows revenue by leveraging the IQVIA offerings and identifying new business opportunities. Essential Functions Develops the skills and knowledge to understand the key priorities of the client to achieve or exceed the assigned revenue and growth goal in assigned account(s) or sales territory.Develops relationships with clients to act as advisor on marketing, market research, sales management, industry issues, trends and IQVIA product, consulting and service capabilities.Anticipates clients’ needs and, in collaboration with IQVIA marketing, sales specialists, consulting and client service, develops and presents proposed solutions to client's complex business issues.Typically interfaces with marketing, market research, sales management and/or IT at the manager level in existing and prospective client(s).Represents the company to the client and the client to the company in all sales related activities.Monitors client satisfaction with contracted deliverables and works with sales management team and Client Service’s management to achieve and maintain a high level of customer satisfaction.Participates in managing renewals and subscriptions.May work with global and regional account management in the pursuit of multi-country opportunities.Qualifications Bachelor's Degree PrefOne (1) year’s relevant sales or account management experience and/or solution sales management experience (preferred) ReqOne (1) year’s relevant sales or account management experience and/or solution sales management experience (preferred)IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $38,100.00 - $95,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

The Senior Manager, Biosamples Operations Lead will own end-to-end biosample operations across assigned studies/programs - from operational feasibility, vendor selection, and execution of biosample operations activities through analysis and data delivery. As the primary point of contact for the Study Team on all biosample operations activities, including biomarker and bioanalytical operational activities, you will ensure every biosample is collected, processed, and delivered to the highest quality and regulatory standard, while keeping a sharp focus on patient burden and operational efficiency. Main Responsibilities• Provides strategic and expert input for the operational feasibility, implementation and execution of the biosample operations activities in assigned clinical studies/programs.• Manages biosample management activities in clinical studies with low to moderatecomplexity, risk, impact and reach.• Accountable for planning, implementation and execution of biosample operations activities, ensuring proactive risks and issues management and alignment with overall clinical study timelines• Owns biosample operations plan and is responsible for its maintenance and adjustments during clinical study conduct.• Leads cross-functional biosample operations team and manage team meetings to review status of biosample operations activities, discuss risks/issues and agree on appropriate mitigation.• Acts as the single point of contact (POC) in Study Team on biosample operations related aspects (including biomarker and bioanalytical activities). Ensures timely status updates and escalation of risks/issues to the clinical Study Team.• Contributes to central lab or assay lab vendor selection and qualification.• Oversees Central lab set-up, kit management, and ongoing study level vendor performance.• Manages CRO and central lab interfaces to ensure cross-functional alignment on deliverables.• Maintains a patient focus approach while delivering the complex requirements of a clinical study, balancing patient burden, sampling requirements, the complexity of collection and the cost implications.• Responsible for overseeing the biosample lifecycle and compliance to ensure that the biosamples are collected, processed, analysed and stored with the highest degree of quality and according to applicable regulations.• Reviews and provides input to protocols, ICFs, lab manuals, and regulatory submissions.• Leads budget planning & forecasting for biosample activities of assigned studies.• Ensures all activities comply with ICH-GCP, GCLP, biobanking policies, and applicable ethical standards.• Leads audit and inspection readiness; act as interviewee and prepare regulatory responses.• Impacts the successful delivery of a program/study and ensure optimized execution of the biosample/biomarker operations strategy on time, within budget and required quality.• Leverages strategic operational knowledge and serves as subject matter expert for current biosample management processes and regulations.  Required Skills and Education• Minimum Bachelor’s degree in Biology, Pharmaceuticals, or Life Sciences or related field. • At least 6+ years of experience in Clinical Operations with a focus on Biosamples management activities in a CRO or pharma setting.• Proven track record in central lab oversight, vendor management, and Phase I–III biosample logistics. • Experience in CDx development and/or Bioanalytical requirements, would be advantageous.• Broad experience across multiple therapeutic areas, trial phases and biosample lifecycle management.• Comprehensive and working knowledge of GCP, GCLP guidelines and other relevant regulations and requirements for the collection, analysis and storage of clinical biosamples.• Very good knowledge of biosample management related systems and technologies (LIMS, BRICK, CTMS, etc)• Demonstrated experience in effectively collaborating with other functions in a complex matrix organization. • Very good command in English language. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 225 500,00 zł - 418 600,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewManages multiple teams of professional-level employees and/or managers.Develops and communicates objectives and priorities to meet the organization's plan and results requirements. Essential Functions• Manages multiple teams of professional-level employees and/or managers and ensures that a consistent design, deployment, and maintenance process is followed for all sites and systems.• Develops and communicates objectives and priorities to meet the organization's plan and results requirements.• Establishes organization-wide budgets, policies and practices with significant impact on area operations.• Influences decision-making at the management and executive level.• Provides coaching and guidance on job performance and career development to direct reports; models and provides leadership examples for organization. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req• Experienced in migrating legacy dashboards to new environments and identifying opportunities to leverage the newer features• Has led small development teams (3-6 developers) for Tableau/Analytics solutions driving both excellence in delivery and mentorship of the team• Have experience with developing career progression plans for a team IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Location: Nagpur Job OverviewMaximize sales growth in a specified geographical territory, consistent with Company strategy and objectives. This is generally achieved by educating and informing physicians and/or hospital staff on the features and benefits the customer’s product(s) versus competitor products in order to increase prescriptions and/or use by the healthcare professionals. Essential Functions• Achieve assigned activity goals and targets for the territory as agreed with the reporting manager, with an initial high level of supervision and coaching provided by the company, customer and manager.• Conduct sales interviews, carry out pre-call planning and preparation and develop a self analytical approach in order to identify learning areas from each call.• Promote and sell customer’s therapeutic products to general practitioners, other identified healthcare providers, and/ or other healthcare professionals in the retail market.• Within a specific geographical territory, identify target customers while maintaining and analyzing customer records.• Maintain records in the reporting systems within the required timescales.• Effectively utilize the relevant software (e.g. Electronic Territory Management System, CRM systems) to maintain records updated and to report daily calls.• Organize and hold group events to optimize business while complying with relevant country legislation.• Keep Line Manager informed about changes in competitor activities and other market changes.• Maintain an up-to-date sales / technical knowledge of specialty and disease areas and relevant publications as per customer profile.• Keep all Company equipment safe and in a good state of repair.• Share experiences, ideas and techniques in order to assist with the sales training of colleagues.• Discuss, agree and document assigned activity, Key Performance Indicator tools, and targets as agreed with Line Manager.• Successfully complete career development courses and additional training as required by the customer.• Ensure the reporting of any identified Adverse Events in line with prevailing process and guidelines.• Project a professional impression of the Company and act in accordance with the relevant Pharmaceutical Industry’s Code of Practice• Perform other duties as assigned. Qualifications• High School Diploma or equivalent 5 years’ relevant experience Req Or• Bachelor's Degree Life Sciences or related field Req• Equivalent combination of education, training and experience may be accepted in lieu of educational requirements Req• Basic knowledge of Pharma Market and related procedures.• Fluency software operating systems, such as MS Office and customer relationship management systems.• Effective verbal and written communication skills.• Ability to conduct face to face presentations to customers.• Ability to prioritize and coordinate multiple work requirements to meet deadlines.• Ability to establish and maintain effective working relationships with co-workers, managers and clients.•  Make plans to obtain any industry qualifications essential to function as a Medical Representative in the relevant market.  Req• AZDL  - Driver Licence - Valid And In State   Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers Essential Functions • Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.• May be responsible for delivery and management of smaller, less complex, regional studies.• Develop integrated study management plans with the core project team.• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.• Set objectives of the core project team and/or sub-team(s) according to agree upon contract, strategy and approach, effectively communicate and assess performance.• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;• Ensure the financial success of the project.• Forecast and identify opportunities to accelerate activities to bring revenue forward.• Identify changes in scope and manage change control process as necessary.• Identify lessons learned and implement best practices.• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.• Adopt corporate initiatives and changes and serve as a change advocate when necessary.• Provide input to line managers of their project team members’ performance relative to project tasks.• Support staff development and mentor less experienced project team members on assigned projects to support their professional development. Qualifications • Bachelor's Degree Life sciences or related field Req• 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience. Req• Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience. Req• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.• Problem solving - Strong problem-solving skills.• Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.• Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.• Organization - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.• Prioritization - Ability to handle conflicting priorities.• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.• Quality - demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.• IT skills - good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.• Finances - Good understanding of project financials including experience managing, contractual obligations and implications.• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

[The final job title will be determined after the interview evaluation.] Job Overview Secure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Essential Functions ● Actively prospect and leverage potential new business opportunities within specified customer account(s). ● Cultivate strong, long-term relationships with key decision-makers within Account and develop in-depth knowledge of the customer organization. ● Maintain general knowledge of all IQVIA services for appropriate cross-sell opportunities. ● Aggressively pursue awareness of competitive activities, positioning and pricing, which includes specific reasons for awards and non-awards. ● Identify and respond to customer needs in order to define potential opportunities. Propose appropriate strategy/solution to customer. ● Coordinate with contracts/proposals to develop proposal. ● Work with operations and functional managers to identify sales team and prepares and leads the sales presentation. Educate team participants in customer culture, operational needs/methods and sales techniques needed to close the sale. ● Handle follow-up related to the sale and drive completion of contractual documents. ● Adapt successful strategies and tactics to meet market demands and financial targets. ● Maintain high visibility within customer organization. Monitor customer satisfaction by communicating regularly with customer. ● Establish and execute a comprehensive sales plan for each target account. Ensure appropriate strategy/solution is proposed to customer. Monitor actions and results against plans. ● Analyze potential opportunities and develop sales plans for each target account. Ensure appropriate strategy/solution is proposed to customer. ● Monitor actions and results against plans. ● Record all customer sales related activities in CRM system. ● Prepare sales activity report for Sales Management as required. ● Serve as a liaison between the customer and technical and operational groups at IQVIA, Inc. Qualifications ● Bachelor's Degree in Business Management ● 5-10 years related experience, including 3 years of relevant industry (CRO/Pharmaceutical) and/or sales experience ● Equivalent combination of education, training and experience Req ● Proven track record at mid-level and high-level contacts ● Strong organizational, planning, project management skills ● A developing record of customer contacts at the outsourcing, procurement and mid - management level ● Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business ● Excellent analytical skills in assessing and interpreting customer business data ● Ability to maintain demanding timelines ● Ability to influence others internally and externally ● Adaptability and flexibility to changing priorities ● Demonstrated ability to work creatively in a fast-paced environment ● Exceptional attention to detail and ability to work simultaneously on multiple priorities ● Ability to work independently and as a team player ● Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel ● Excellent oral and written communication skills ● Ability to establish and maintain effective working relationships with coworkers, managers and clients IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Manila Speaker Bureau Financial Close & Review Planner IQVIA’s Speaker Bureau team consists of dedicated meeting professionals who plan and manage highly compliant meetings and events for Life Sciences organizations.  We work with our clients to deliver a high-quality attendee experience through a range of in-person, hybrid, and virtual meetings by seamlessly pairing deep industry expertise, best-in-class compliance technology and an innovative, scalable approach to support our client’s Speaker Bureau.  The Manila Speaker Bureau Financial Close & Review Planner is overall accountable in auditing and reviewing actual financials post meeting. FCR Planner is heavily focused on ensuring we are accurate in our government required Transfer of Value reporting responsibilities. Essential Duties & Responsibilities Collaborate as an integral part of the client Core Team which comprises of meeting planners, logistics planner and speaker bureau planners and other roles supporting execution of planning of each meetingReview all aspects of planning are within the client’s business rules and budgetary requirement. The following items are critical to the FCR Planner role in executing seamlessly:Assess accuracy of Management Fee applied tied to the program typeReview Speaker Travel expenses to ensure no discrepancy between itinerary vs travel chargesReview Speaker Honorarium to ensure Speaker is paid correctly.Accurately plot venue/caterer charges to the specific FCR approved calculator to flag any overage on approved cost per person as neededAccurately move charges to their applicable budget category following client’s business rules on approved categoriesReview and resolve attendance discrepancies as needed.Ensure all expenses matches between systems (EFX and Centris) and document approved exemptions as neededObtain necessary documents (receipts) are uploaded in the meeting and other related documents as requiredCommunicate timely with meeting planner, speaker bureau planner, logistics planner, vendors related to task completion and other related inquiry or follow up needsApplication of client business and compliance rules throughout the financial close & review process.Ability to trigger or escalate any items that can impact risk on meeting compliance.Ensure understanding of system functionalities related to job function as assigned.Liaise with relevant internal and external stakeholders to ensure appropriate team members have the most up to date informationComply with timekeeping standards & policies in Sprout, PSA ensuring accurate work hours are logged.Other related team task maybe assignedQualifications 2+ years of customer service or equivalentPrevious work experience in catering to US clients, preferably in a phone-based Customer Service role, is requiredRelevant audit experience is preferredPharma Industry experience is a plusFamiliarity with US cultural norms and practices to better understand and service stakeholders and clients. Bachelor's Degree RequiredProficiency in PC applications, Microsoft Office suite of products (Word, Excel, PowerPoint, Teams) and Outlook is requiredKnowledge in SharePoint, Salesforce and Smartsheet preferredProficiency in using phone systems such as Twilio, CRM software and other relevant technology is preferredAble to work during US standard business hours and be flexible on work schedule and/or extended hours to meet clients’ business needs during peak seasonExpert on analysis and information gathering to resolve problems on routine matters.Ability to multi-task/plan numerous meetings simultaneously while still demonstrating a strong attention to detailComfortable working in a fast-paced team environment, while also able to work independentlyExceptional customer service skillsA strong sense of urgency and the ability to effectively problem solveExcellent in communication, both oral and writtenCollaborate as an integral part of the project team to execute world class events as measured by internal and external client satisfactionStrong aptitude of financial calculations.A strong sense of urgency and advanced ability to effectively problem solve.Advanced oral and written communication skills with focus on the ability to be concise and clear, summarize a situation and articulate the necessary next steps, effectively listen, and assess the need for urgent action.Able to be flexible to report onsite frequently, dependent on business needConducive work space when working remotely at home, which includes ability to receive and make calls during your shift, work with company provided dual monitors and have appropriate internet speed to complete work.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für unseren Kunden, ein renommiertes, international agierendes Familienunternehmen, suchen wir zum nächstmöglichen Zeitpunkt einen Pharmaberater (m/w/d) General Medicine / Diabetes Im Gebiet: Stuttgart, Ludwigsburg, Leonberg Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du die Verordnung Deiner Präparate und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte in anspruchsvollen Indikationen. (optional: zum Wohle des Patienten/für den Patienten/und trägst somit zur Gesundheit und dem Patientenwohl bei) Du führst regionale und zentrale Fortbildungsveranstaltungen in enger Abstimmung mit dem Regionalleiter und Deinem regionalen Team durch. Das bringst Du mit: Du hast idealerweise bereits erste Erfahrung im Pharma-Außendienst gesammelt, idealerweise in der Indikation Diabetes. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, Dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für Dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Du kannst mit digitalen Medien gut umgehen und hast solide Kenntnisse, um auch englische Fachtexte zu verstehen. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater; #Biologie; #Chemie; #Pharmareferent; #BTA; #CTA; #PTA; #Oecotrophologie; #Pharmazie; #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join IQVIA's Nordic Consulting Team | Stockholm Are you passionate about improving patient access to innovative medicines and helping shape the future of healthcare in Sweden? IQVIA is looking for an experienced Associate Director, Value & Access Consulting to join our growing Nordic consulting team at Forskaren in Stockholm. This is a senior, client-facing role for a market access expert who thrives on combining strategic thinking, scientific evidence, and commercial insight to support life sciences companies across Sweden and the Nordics. As a trusted advisor, you will lead consulting engagements focused on market access, reimbursement, HTA, health economics, and evidence generation. You will work closely with clients to develop evidence-based access strategies while contributing to the growth and development of IQVIA's Nordic Value & Access practice. What You'll Do Lead Strategic Client Engagements Serve as a senior advisor to life sciences clients on market access, reimbursement, HTA, and pricing strategy.Lead and deliver high-quality consulting projects across Sweden and the Nordics.Manage cross-functional project teams and ensure excellence in delivery and client satisfaction.Present strategic recommendations and insights to senior client stakeholders.Drive Value & Access Excellence Lead projects covering market access strategy, launch planning, reimbursement pathways, value communication, and health economic evidence.Advise clients on Swedish and Nordic payer and HTA requirements, with a particular focus on the Swedish market.Support the development and adaptation of health economic and outcomes evidence, including cost-effectiveness and budget impact models.Identify evidence gaps and support real-world evidence strategies that strengthen value demonstration and payer engagement.Contribute to stakeholder engagement activities, advisory boards, and market access implementation at national and regional levels.Contribute to Business Growth Approximately 30-40% of the role is dedicated to business development. Build and strengthen relationships with clients and key market access stakeholders.Identify new business opportunities and develop consulting proposals.Contribute to the growth of IQVIA's Nordic Value & Access offering by combining local expertise, data, analytics, and global capabilities.Mentor and support colleagues, helping develop capabilities across the consulting team.About You Bachelor's degree required; Master's degree preferred.8-12 years of experience within life sciences, consulting, market access, HTA, HEOR, health economics, pricing, or reimbursement.Strong expertise in the Swedish market access and payer environment.Experience from one or more additional Nordic markets is an advantage.Proven ability to lead complex projects and manage multiple priorities.Excellent communication, presentation, and relationship-building skills.Established network within the life sciences and market access community.Collaborative, entrepreneurial, and motivated by delivering meaningful impact for clients and patients.Why IQVIA? At IQVIA, you'll join a highly experienced and collaborative Nordic consulting team with access to world-leading healthcare data, analytics, and global expertise. You'll have the opportunity to work on some of the industry's most important challenges - helping innovative treatments reach the patients who need them while shaping the future of healthcare across the Nordics. If you're ready to combine your market access expertise with strategic consulting and business leadership, we'd love to hear from you. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvides support to CMS leads  on activities related to the CMS team, in partnership with project and clinical lead, and in collaboration with other functional teams, to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies and practices. Associate Centralized Monitoring Lead has particular focus on supporting the centralized team functionally reporting to leads towards solutions to clinical risks identified and working towards successful implementation of those strategies to address the issues. Support in efficient and effective review of Site Visit Reports and assure consistent standards of implementation for quality to meet or exceed quality standards. Ensure subject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SOP, ICH/ GCP guidelines, protocol requirements and regulatory compliance. Review of the Study Central Monitoring Plan Essential Functions Provide support to CMS leads on clinical deliverables on assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operation Plan (COP) from Applications/ Analytics/ Therapeutics/ Quality perspective.; May perform functional lead responsibilities for assigned project deliverables for certain smaller or less complex projects from start-up to final deliverables including closeout.; Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested and note CMS specific action items.; Support CMS Lead to oversee the Finance related information in the study and provide inputs to EAC.; May manage Investigator Payment Activity from set up to close out of the study.; Contribute to the development and use of study management plans including Risk Assessment and Mitigation Plan, specific tools and document templates and/or other study specific plans to evaluate the quality and integrity of the study, including complete and accurate documentation so that the project is audit ready.; Support CMS Lead/project team to develop monitoring strategy including monitoring triggers/thresholds, and the study specific analytics strategy, work on developing analytics based on applicable study specific plans, develop new analytics proposal as per customers demand, Perform quality reviews on the analytical output created by the team members. Manage operational insight of the assigned project(s) and perform the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and discuss the action plan, review, triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.). Provide Inputs to CMS Lead/Project team, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections. Identify the value adds from the centralized review & remote monitoring in the study and provide the inputs to relevant stakeholders. Support in managing project resources (CRAs/CTAs/Centralized monitoring team). Support in performing the IP management for the assigned study to identify risk and propose mitigation plan, if any (including re-supply, re-labelling, Import/export licenses etc.). Conduct periodic review of site level KRIs and historic site performance according to Central Monitoring Plan and enable early identification of site-level risk/issue(s) and take appropriate action. Monitor operational triggers/Key Data Points/data trends and monitor their compliance check by performing regular Quality Check. Evaluate the quality and integrity of site practices related to the proper conduct of the study as per protocol. Create and maintain relevant project documents/ trackers. Ensure accurate completion and maintenance of internal systems, tracking tools and timelines. Coordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles. Act as lead for the reviewers performing Subject Level Data Review, create plans to review the clinical data of subjects in accordance with project requirements, maintain study metrics on delivery and quality. Perform regular quality checks for the data reviewed at subject-level. Participate in (study) team meetings/Project kick off meetings and interaction with cross functional staff to verify information and/or triage new data issues. Review site visit reports per annotations, SOPs, guidelines etc., identifies issues and escalates the same to the Clinical Lead, assists with creating annotations, CRA trainings, support to conducts monthly calls with relevant stakeholders to discuss major issues emerging from the trends noted during report review. May require to mentor or coach for junior CMS staff and foster ownership and collaboration with the team. Act as back up to CMS leads on assigned projects. May contribute as Subject Matter Expert to support the CMS department in delivering trainings, perform periodic review of Centralized monitoring trainings and/or identify the training needs of the team and provide inputs whenever required. Act as a technical solution specialist (TSS) point of contact to connect with the project teams/internal stake holders for gathering the criteria and requirements. Analyze the complexity of the requirements and provide the EAC hours and turnaround time. Monitor site performance and make recommendations for timely corrective actions (e.g. Site Telephone Contact or Triggered Onsite Monitoring Visit). Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observed. Work in accordance of the Study Central Monitoring Plan Adhere to the key activities outlined in the SOW as per customer requirements. Qualifications Bachelor's Degree Clinical, life sciences, mathematical sciences, or related field, or nursing qualification. Minimum 4 years of relevant work experience or equivalent combination of education, training, and experience. At least 2 years of experience in clinical research field or centralized monitor role preferred. Experience level may vary based on customer specific requirements. Good knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Good Clinical system expertise. Strong written and verbal communication skills including good command of English language. Results and detail-oriented approach to work delivery and output. Understanding of clinical/medical data.; Good motivational, influencing, negotiating and coaching skills. Ability to work on multiple projects and manage competing priorities. In depth therapeutic and protocol knowledge.; Strong organizational, problem solving and decision-making skills. Demonstrated ability to deliver results to the appropriate quality and timeline metrics. Effective presentation skills. Ability to work across cultures and geographies with a high awareness and understanding of cultural differences and maintain effective working relationships with co-workers, managers and clients. Demonstrated ability to deliver results to the appropriate quality and timeline metrics. Ability to effectively work in team. Extensive use of keyboard requiring repetitive motion of fingers. Extensive use of telephone and face-to-face communication requiring accurate perception of speech. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Local: Regiões estratégicas do território nacionalModelo de atuação: Externo | Visitação PresencialRegime de contratação: CLT Sobre a posiçãoBuscamos um(a) profissional da área da saúde para atuar na geração de demanda e no relacionamento científico com profissionais de saúde em hospitais, clínicas e instituições estratégicas. O objetivo da posição é ampliar o conhecimento sobre terapias especializadas, promover educação científica, apoiar treinamentos técnicos junto às equipes assistenciais e desenvolver relacionamentos sustentáveis com stakeholders relevantes, contribuindo para os resultados do projeto e para a qualidade do atendimento aos pacientes. Principais responsabilidades - Realizar visitas presenciais a médicos, enfermeiros e demais profissionais de saúde.- Promover conteúdos técnico-científicos e apoiar iniciativas de educação continuada.- Ministrar treinamentos técnicos para equipes assistenciais e de enfermagem.- Desenvolver e fortalecer relacionamentos com stakeholders estratégicos das instituições atendidas.- Executar o plano de visitas e garantir cobertura adequada do território.- Registrar atividades e oportunidades em sistema CRM.- Acompanhar indicadores de produtividade, cobertura, frequência e execução.- Identificar oportunidades de negócios e compartilhar insights de mercado.- Participar de eventos científicos, treinamentos e reuniões periódicas.- Atuar em conformidade com as diretrizes de ética, compliance e regulamentação do setor farmacêutico. Requisitos - Ensino superior completo em Farmácia, Enfermagem, Biomedicina ou áreas correlatas da saúde.- Experiência em visitação médica com promoção científica na indústria farmacêutica.- Vivência no ambiente hospitalar e institucional será considerada um diferencial.- Experiência com treinamentos técnicos e educação para profissionais de saúde será valorizada.- Conhecimento de ferramentas de CRM, gestão de território e indicadores de desempenho.- CNH ativa e disponibilidade para deslocamentos frequentes e viagens.- Excelente comunicação, capacidade de influência e habilidade para construção de relacionamento.- Perfil consultivo, analítico e orientado para resultados.- Organização, planejamento e gestão eficiente de prioridades.- Proatividade, autonomia e senso de dono.- Adaptabilidade para atuar em ambientes dinâmicos e projetos de alta visibilidade.- Compromisso com ética, compliance e excelência na execução A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! #LI-CES #LI-DNP #LI-LATAM IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Localização: Preferencialmente em regiões com fácil acesso a aeroportos e ampla conectividade aéreaModelo de atuação: Campo | Viagens frequentesRegime de contratação: CLT Sobre a oportunidadeBuscamos um(a) Consultor(a) Científico(a) para atuar como referência técnico-científica junto a profissionais de saúde, principais especialistas e stakeholders do ecossistema de saúde. Este profissional será responsável por construir relacionamentos científicos estratégicos, disseminar conhecimento médico de alta qualidade e apoiar iniciativas de educação científica em diferentes áreas terapêuticas. A posição exige forte capacidade analítica, elevado conhecimento técnico, excelente habilidade de comunicação e disponibilidade para uma rotina dinâmica, com intensa atuação em campo e interação constante com especialistas. Principais responsabilidades - Desenvolver e manter relacionamento científico com médicos, pesquisadores, líderes de opinião (KOLs) e demais stakeholders estratégicos.- Realizar discussões científicas aprofundadas sobre doenças, evidências clínicas e terapias.- Apoiar iniciativas de educação médica e atualização científica.- Mapear oportunidades e gerar insights relevantes provenientes do campo.- Participar de congressos, eventos científicos e reuniões médicas.- Fornecer suporte técnico-científico às áreas internas quando necessário.- Identificar tendências, necessidades não atendidas e oportunidades de desenvolvimento científico.- Atuar de forma ética e em conformidade com as diretrizes regulatórias e de compliance aplicáveis.- Gerenciar múltiplas demandas e áreas terapêuticas de maneira organizada e estratégica. Requisitos - Graduação completa na área da saúde (Farmácia, Nutrição, Biomedicina, Biologia e outras)- Perfil técnico-científico sólido.- Experiência prévia em funções científicas, médicas, clínicas ou correlatas será considerada um diferencial.- Conhecimento ou experiência em doenças raras será um diferencial relevante.- Capacidade de compreender e comunicar conteúdos científicos complexos para diferentes públicos.- Excelente comunicação verbal, escrita e habilidade para construção de relacionamento.- Perfil organizado, proativo e com alta capacidade de planejamento.- Facilidade para atuar com autonomia e gerenciamento de agenda.- Capacidade de trabalhar em ambientes dinâmicos e lidar com múltiplas áreas terapêuticas simultaneamente.- Disponibilidade para viagens frequentes e atuação em campo aproximadamente 4 dias por semana.- Residir em localidades com boa malha aérea para suporte às necessidades de deslocamento da posição. - Possuir veículo próprio e disponibilidade para utilizá-lo nas atividades profissionais e deslocamentos da região de atuação.- CNH válida e regular. A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! #LI-CES #LI-DNP #LI-LATAM IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

External Job DescriptionAtividades: Suporte na gestão de projetos de pesquisa de mercado Desenvolver questionários de pesquisa de mercado Analisar as respostas dos médicos às questões de pesquisa de mercado Elaboração de gráficos que mostrem claramente os resultados Montagem de apresentações finais com insights, análises e recomendações Realizar análises competitivas Requisitos: Graduação completa em  Marketing, Comunicação, Ciências da Saúde e correlatos Bons conhecimentos em Excel e PowerPoint Experiência em pesquisa de mercado  Experiência na indústria farmacêutica será um diferencial Inglês intermediário Disponibilidade para trabalhar no modelo híbrido em São Paulo/Capital (4x presencial) A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Sobre a posiçãoEstamos em busca de um(a) E-MSL (Electronic Medical Science Liaison) para atuar como um importante elo entre a área médica e os profissionais de saúde, promovendo intercâmbios científicos de alta qualidade por meio de canais digitais e presenciais. Buscamos um perfil com forte embasamento científico, excelente comunicação e conforto em ambientes dinâmicos, que exijam alto volume de interações, agilidade nas respostas e uso constante de ferramentas digitais. Principais responsabilidades - Conduzir interações científicas com profissionais de saúde por meio de canais digitais e remotos.- Fornecer informações médicas e científicas de forma clara, precisa e alinhada às estratégias da área médica.- Desenvolver e manter relacionamentos sólidos com stakeholders internos e externos.- Apoiar eventos científicos, reuniões médicas e iniciativas de engajamento com a comunidade médica.- Gerenciar múltiplas demandas simultaneamente, garantindo qualidade e cumprimento dos prazos de resposta.- Colaborar com equipes locais e globais para compartilhamento de conhecimento e melhores práticas. Requisitos - Graduação completa na área da Saúde (Farmácia, Biomedicina, Medicina, Enfermagem ou áreas correlatas).- Boa capacidade de interpretação e comunicação científica.- Familiaridade com interações digitais e gestão de alto volume de contatos.- Inglês avançado, com capacidade de comunicação em contexto profissional.- Fluência digital e facilidade no uso de ferramentas tecnológicas, especialmente Microsoft Teams e plataformas de comunicação virtual.- Disponibilidade para participação em eventos e interações presenciais quando necessário.- Experiência prévia em Medical Affairs, MSL ou funções de relacionamento científico (diferencial).- Vivência com plataformas digitais de engajamento médico (diferencial).- Participação em projetos globais ou interação com equipes internacionais (diferencial). A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! #LI-CES #LI-DNP #LI-LATAM IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für unseren Kunden, ein renommiertes, international agierendes Familienunternehmen, suchen wir zum nächstmöglichen Zeitpunkt einen Pharmaberater (m/w/d) General Medicine / Diabetes Im Gebiet: Saarbrücken, Homburg, Neunkirch Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du die Verordnung Deiner Präparate und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte in anspruchsvollen Indikationen. (optional: zum Wohle des Patienten/für den Patienten/und trägst somit zur Gesundheit und dem Patientenwohl bei) Du führst regionale und zentrale Fortbildungsveranstaltungen in enger Abstimmung mit dem Regionalleiter und Deinem regionalen Team durch. Das bringst Du mit: Du hast idealerweise bereits erste Erfahrung im Pharma-Außendienst gesammelt, idealerweise in der Indikation Diabetes. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, Dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für Dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Du kannst mit digitalen Medien gut umgehen und hast solide Kenntnisse, um auch englische Fachtexte zu verstehen. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater; #Biologie; #Chemie; #Pharmareferent; #BTA; #CTA; #PTA; #Oecotrophologie; #Pharmazie; #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewResponsible to perform spirometry and other Pulmonary function tests overread for records received from trial sites as per study specific requirements and latest ATS/ERS Guidelines . Job Responsibilities: To perform Spirometry/Pulmonary function tests overread and proficiency review. Understand and comply with core operating procedures and work instructions of Connected Devices. Maintain operational responsibility for managing study specific requirements. Assist in the induction process, mentoring and training of new Primary analyst- Spirometry. Qualifications: Registered Respiratory Therapist (RRT) or Registered Respiratory Therapist PFT.Pulmonary function technologist, Respiratory physiologist At least 1-year relevant experience in Respiratory physiology and Lung function testing. Computer Literate Ability to work well within a team Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Associate Creative DirectorRole Overview  IQVIA is seeking a highly creative and technically skilled Associate Creative Director to lead the development and execution of innovative visual solutions across our healthcare marketing and communications portfolio. This role will serve as a subject matter expert in emerging creative technologies, including AI-generated art, digital imaging, photo composition, retouching, 3D asset creation, and animation. The Associate Creative Director will partner with senior creative leaders, marketing teams, and agency partners to deliver compelling brand experiences while driving innovation in creative processes and visual storytelling.   Responsibilities  Lead the execution of creative strategy, brand development, and visual asset creation across a broad range of marketing initiatives.  Develop and implement AI-enabled creative workflows and champion the adoption of emerging creative technologies.  Create and oversee the production of AI-generated imagery, photo compositions, retouched photography, 3D assets, animations, and other visual content.  Partner with senior creative leadership to develop breakthrough creative concepts that differentiate brands in the marketplace.  Collaborate with internal stakeholders and external agency partners to deliver high-quality campaign assets and creative solutions.  Lead concept development and execution for branding, advertising, and integrated marketing communications campaigns.  Mentor and develop creative team members, sharing expertise in campaign execution, emerging technologies, and best practices.  Contribute to process improvements and help elevate the overall creative capabilities of the organization.  Qualifications  Bachelor's degree in Graphic Design, Fine Arts, Visual Communications, or a related discipline.  10+ years of experience in a creative agency, in-house creative organization, or similar environment.  4+ years of experience leading, mentoring, or managing creative professionals.  Deep expertise in AI-generated imagery and advanced creative production tools.  Advanced proficiency with Adobe Creative Suite; experience with AI image-generation platforms; expertise in image retouching, photo composition, digital asset creation, 3D modeling, rendering, animation, branding, and visual storytelling.  Why Join IQVIA?  Join a global leader in healthcare intelligence and life sciences, where creativity, technology, and innovation come together to improve human health. You will have the opportunity to shape the future of creative development through AI-powered solutions, work alongside industry-leading talent, and make a meaningful impact on brands and campaigns that reach healthcare professionals and patients worldwide.  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $88,300.00 - $246,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

【会社紹介・ビジョン】 私たちIQVIAは、ヒューマンデータサイエンスの先駆的な企業として、医療・ヘルスケアの前進に取り組む皆様をIQVIAならではの革新的なソリューションによってご支援することで、「誰もが、より健康に自分らしく生きられる社会」の実現を目指しています。世界最大規模を誇る医療・ヘルスケア関連データを基盤に、人・データ・サイエンスを融合させた見地から、未だ満たされない治療ニーズに応える、新たな医薬品や医療機器の開発と市販化、厳格化する規制やコンプライアンスへの対応、持続可能な医療システム推進の支援など、患者さんをはじめとするすべての人々のために、より良い未来へと医療・ヘルスケアを前進させていく力となることが、私たちの使命です。 世界100以上の国と地域で約9万人が活動するIQVIAの日本法人として、IQVIAジャパンでは約6,000人が一丸となり、この使命に向かって日々、力を尽くしています。 【部門】 IQVIAのメディカルインフォメーション部門は、製薬企業のお薬相談室やコンタクトセンターを受託運営し、医療従事者や患者さんからの問い合わせ対応、有害事象情報の収集・報告、品質管理などを担う部門です。 【魅力】 ・グローバルの顧客とコミュニケーションをするため、国際的な仕事ができる ・担当する製品には新薬も多く含まれるため、新しい知識を学ぶことが好きな方には特に面白い環境です。医薬品や医療テクノロジーの進化を間近で感じながら、専門性を高めていくことができます。好奇心旺盛で、常に学び続けたい方におすすめのポジションです。 Grade：Grade140 【担当業務】 ・医療機関や一般からの問い合わせに対し、適切な回答を行う ・メール・電話による有害情報の聞き取り・収集 ・収集・整理した有害事象のクライアントへの報告（システム経由） ・上記業務における品質改善、進捗管理、問題可決、メンバーサポートなどのスーパーバイザー業務 【必須要件】 ・ビジネスレベルの日本語能力・ビジネスレベルの英語力（英語での会議が可能、読み書き可）　※目安：TOEIC850点以上 ＊グローバルの顧客とコミュニケーションが発生するため ・製薬業界でのご経験・医療関係者（医師・薬剤師など）との対応力（スムーズさ、マナーなど） 【歓迎要件】・医薬品業界におけるコンタクトセンター/コールセンター、お薬相談室などでの医療機関対応経験（年数不問）・ライフサイエンス関連の学歴・職歴・添付文書やインタビューフォームの改訂作業をしたことがある・薬剤師もしくはMR資格 【勤務地】 東京または大阪 フルリモート（必要に応じ、東京の顧客オフィスに訪問有） ＊東京にお住まいでない場合には、年1回ほど出張有 必要に応じてオフィス（品川/新大阪）へ出勤 【勤務時間】 標準時間（9:00-17:30) 想定残業時間：月間10～20時間程度 【雇用形態・勤務時間・福利厚生・休日休暇】 雇用形態：正社員 勤務時間：9:00-17:30 在宅勤務制度：あり福利厚生：法定内（社会保険制度）・法定外（IQVIA独自制度）の両面から充実した福利厚生制度あり 受動喫煙対策：あり 休日休暇：年次有給休暇、夏季休暇、病気休暇、特別休暇、女性特別休暇、育児介護休暇、看護休暇·など 試用期間：あり（通常６か月） 【給与・待遇】 給与：当社規定により優遇します 昇給：あり 賞与：あり 時間外手当：あり 【選考プロセス（オンライン完結）】 ①書類提出（履歴書・職務経歴書） ②書類選考 ③人事面談（オンライン） ④部門面接（オンライン） ※状況に応じて変更になる場合がございます IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.