Please note that currently this position is fully on-site at the site in Metairie, Louisiana. This site is scheduled to move to Kenner, Louisiana after September, 2025. Therefore this position will eventually be fully on-site in Kenner, Louisiana.

Join a collaborative, patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role — it’s a unique opportunity to deepen your expertise in clinical trial coordination, grow within a supportive environment that values professional development, and make real progress toward your career goals. It’s an ideal fit for a hardworking, driven, and passionate individual who thrives in a fast-paced, team-oriented setting and is eager to make a meaningful impact through clinical research.

Overview:

Coordinate and participate in clinical research studies ensuring that studies are carried out according to protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.

Essential Functions

Coordinate clinical research studies conducted by a supervising principle investigator.

May assist as back-up CRC on other studies

Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved

Obtains informed consent of research subjects

Develops strong working relationships and maintain effective communication with study team members

Completes all protocol related training

Performs patient/research participant scheduling

Collects patient/research participant history 

Collects and maintains source documentation

Manages inventory and administers test articles/investigational product to participants 

Performs data entry and query resolution

Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.)

Adheres to an IRB approved protocol

Supports the safety of research subjects, report adverse events

Coordinates protocol related research procedures, study visits, and follow-up 

Facilitates pre-study, site qualification, study initiation, monitoring visits, and study close out activities

Collects, processes and ships laboratory specimens

May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs arise

Complies with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines

Performs other duties as assigned

Qualifications

Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines

Clinical Research Coordinator experience within a similar setting preferred

Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.

Knowledge and experience of site operations and the drug development process

Effective communication

Computer proficiency in use of Microsoft Word, Excel

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

The potential base pay range for this role, when annualized, is $36,600.00 - $91,300.00. 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.