Job Description

Clinical Research Coordinator position at an SMO managing multiple clinical trials with exposure to diverse therapeutic areas. Role requires hands-on clinical skills and site operations knowledge, with opportunities for professional development in clinical research.

Responsibilities

• Manage 2–6 concurrent trials of varying complexity from initiation to completion
• Recruit study participants and obtain informed consent per protocol requirements
• Perform clinical procedures and maintain regulatory documentation
• Coordinate with investigators, sponsors, and study monitors on trial activities
• Mentor junior staff and contribute to internal training programs

Requirements

• 1–3 years clinical research experience at investigative site (CRC I) or 3+ years (CRC II)
• Proficiency obtaining vital signs, phlebotomy, ECGs, and lab specimen processing
• Demonstrated experience with pediatric blood draws
• Understanding of site operations and drug development process
• Strong written and verbal communication with attention to detail
• Proficiency with CTMS, eCRFs, and Microsoft Office applications

Compensation: $37,800–$94,500 base annually

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