Clinical Research Coordinator – Germantown, TN
Work Set-Up: On-site
Schedule: Part-time, 24 hours per week

About the Role

We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance. Responsibilities also include working directly with consenting patients, conducting study visits, processing laboratory samples, and performing ambulatory blood pressure monitor (ABPM) procedures. Accurate and timely data entry will be an essential part of this role.

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

Key Responsibilities

• Perform a variety of complex clinical procedures, including ECG, spirometry, sample collection, and vital signs.

• Phlebotomy is required; pediatric experience is highly preferred.

• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.

• Conduct patient consenting and perform study visits in accordance with study protocols.

• Process laboratory samples and perform ABPM (ambulatory blood pressure monitor) procedures.

• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.

• Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study.

• Collect and accurately record clinical data in case report forms (CRFs); complete timely and high‑quality data entry.

• Collaborate with investigators and monitors, addressing queries and ensuring data quality.

• Act as a volunteer advocate and maintain a safe environment in accordance with Health and Safety policies.

Qualifications

• High School Diploma or equivalent education and experience.

• Minimum 1 year of relevant work experience in clinical research (preferred).

• Working knowledge of clinical trials, GCP principles, and medical terminology.

• Strong attention to detail and ability to establish effective working relationships.

• Experience with CRIO is a plus.

• Experience with Allscripts/Altera EMR is a plus.

Please note: This position is not eligible for sponsorship.

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