Clinical Research Coordinator

Regulatory Jobs; Jefferson City (MO); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA in Jefferson City, MO is seeking a Clinical Research Coordinator to join our team on-site. This role involves performing clinical procedures, coordinating studies, and ensuring compliance with GCP guidelines under the supervision of a principal investigator.

Responsibilities include ECGs, sample collection, patient recruitment and data entry into CRFs, plus collaboration with investigators and monitors to maintain data quality and patient safety.

Qualifications

• Bachelor’s degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to establish effective working relationships.
• Proficiency with EDC systems, data entry accuracy, and query management.

Responsibilities

• Perform ECG, sample collection, and vital signs.
• Coordinate clinical research studies and ensure GCP compliance.
• Prepare study materials, set up equipment, and plan logistical activities.
• Recruit, screen, and orient patients, ensuring their safety and well‑being.
• Collect and record clinical data in case report forms (CRFs).
• Collaborate with investigators and monitors, addressing queries and ensuring data quality.
• Act as a patient advocate and maintain a safe environment per Health and Safety policies.

Skills

Attention to detail

Data entry accuracy

Communication skills

Team collaboration

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

Clinical Research Coordinator – Jefferson City, MO

Work Set-Up: On-site
Schedule Weekly Hours: 24 hours/week

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.

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.

Key Responsibilities

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

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

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

• Recruit, screen, and orient patients, ensuring their safety and well‑being throughout the study.

• Collect and accurately record clinical data in case report forms (CRFs).

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

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

Qualifications

• Bachelor’s degree preferred or equivalent combination of education and relevant experience.

• Minimum 1+ years of relevant work experience in clinical research.

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

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

• Proficiency with EDC systems, data entry accuracy, and query management.

Please note: This position is not eligible for sponsorship.

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 $35.00-$42.00 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.