Role OverviewThe Clinical Research Coordinator is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards. The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.
What You Will Do
Key responsibilities include study management & coordination, recruitment, enrollment & consent, clinical oversight & subject monitoring, documentation, data & systems, investigational product & specimen management, quality, compliance & team support, and communication & outreach.
Why It Might Be a Fit
The ideal candidate will have strong leadership and communication skills, exceptional organizational and multitasking abilities, high attention to detail, and a commitment to regulatory compliance. Experience in clinical research or clinical trial management is required, and a Bachelor's degree in a related field is preferred.
Requirements
- Strong leadership and communication skills
- Exceptional organizational and multitasking abilities
- High attention to detail and commitment to regulatory compliance
- Ability to work independently and collaboratively in a multidisciplinary environment
- Strong time management and operational efficiency skills
- Proficiency with office equipment and study-specific systems
- Ability to maintain strict confidentiality
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