Clinical Research Coordinator - Columbia, MD
About The Position
Clinical Research Coordinator – Columbia, MD Work Setup: On-site Schedule: Part-time (32 hours per week) Shape the Future of Medicine with IQVIA! Are you passionate about advancing healthcare and improving patient outcomes? Join IQVIA as a Clinical Research Coordinator (CRC) and play a vital role in supporting clinical research studies that drive meaningful innovation. This hands-on role blends clinical procedures, patient recruitment, and study compliance to ensure the highest standards of safety and care. About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient lives. Our teams combine scientific expertise with advanced technology to transform clinical trials and healthcare delivery.
Requirements
- High School Diploma or equivalent education/experience
- Minimum 1 year of relevant clinical research experience (preferred)
- Working knowledge of clinical trials, GCP principles, and medical terminology
- Strong attention to detail and ability to build effective working relationships
- Recruitment-focused with strong patient-facing experience as a Clinical Research Coordinator (CRC)
- Demonstrated knowledge of the full study lifecycle from start-up to close-out
- Hands-on experience performing CRC tasks in a clinic setting
- Skilled in patient recruitment, prescreening, and using study protocols to identify inclusion/exclusion criteria
- Proficient with Electronic Data Capture (EDC) systems and query resolution
- Experience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referrals
- Experience in both research and clinical settings
Nice To Haves
- Regulatory experience is a plus
Responsibilities
- Perform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signs
- Coordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP)
- Prepare study materials, manage logistics, and support overall site operations
- Recruit, pre-screen, and orient volunteers, including chart reviews, physician referrals, and community outreach
- Communicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteria
- Collect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs), including corrections and query resolution
- Assist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study-related issues
- Maintain a safe environment for volunteers in alignment with Health & Safety policies
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees
