Clinical Research Coordinator, On-Site
About The Position
Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. At Avacare, CRCs wear multiple hats, gaining experience across various therapeutic areas, managing complex protocols, and taking ownership of key trial activities. This role offers the opportunity to strengthen core CRC skills and prepare for future roles in clinical operations, monitoring, and beyond. The position is with IQVIA, a leading global provider of clinical research services, commercial insights, and healthcare intelligence.
Requirements
- Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
- Solid understanding of site operations and the drug development process.
- CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.
- CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.
- Strong written and verbal communication skills, with attention to detail and time management.
- Comfortable using CTMS, eCRFs, and Microsoft Office tools.
Responsibilities
- Manage 2-6 trials of varying complexity.
- Perform clinical procedures.
- Lead study coordination from start to finish.
- Work closely with investigators, sponsors, and monitors.
- Mentor junior staff.
- Contribute to internal training.
- Obtain vital signs.
- Perform phlebotomy.
- Conduct ECGs.
- Process lab specimens.
Benefits
- Health and welfare benefits
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
