Work Set-Up: Local Travel – In patient Home

Are you a Registered Nurse interested in Clinical Trial work?

IQVIA is looking for qualified Registered Nurses interested in community and clinical trial work to visit clinical trial patients in their homes. You will be responsible for going to patient homes to assist with conducting research, collecting data and samples to help evaluate safety/efficacy of a new medication.

The visits/hours can be arranged to suit your current work schedule but need to be in the morning/early afternoon. Preferably we look for PRN Nurses or Nurses who already work part time.

Responsibilities

• Complete all reports and written assignments in a timely, accurate, and thorough manner per set timelines and customer expectations.

• Maintain a high level of professional standards in all interactions with patients and customer contacts.

• Read, understand, and adhere to important documents such as fraud and abuse guidelines, FDA guidelines, Pharma code, and HIPAA guidelines and memos regarding policy and procedures.

Role of Nurse During Visit:

• Collecting samples and required information and data.

• Drawing blood, taking vitals, and conducting urine tests.

• Administering medication if needed.

• Labeling and shipment of samples.

• Reporting of adverse events.

• Inputting reporting and event notes post-assignment.

• Tasks can vary depending on the trial.

Requirements:

• Active RN license in home state.

• BLS certification required.

• Must be comfortable with basic software programs.

• Recent experience in drawing blood.

• Flexible with your time and available on short notice.

• Ability to travel regionally by car, and willing to travel up to 90 miles if needed.

• Possess a cellular phone, reliable transportation, and access to the internet.

• Ability to stand for long periods of time; bending or kneeling may be required.

You will have a flexible schedule, an opportunity to travel, grow, and expand into new opportunities while earning supplemental income and gaining exposure to clinical trials.

Please note, this position is not eligible for sponsorship.