Senior Clinical Research Coordinator

Responsibilities: of the Senior Clinical Research Coordinator include: · Oversee clinical studies throughout the full research lifecycle, from site initiation through study closeout. · Coordinate participant recruitment, screening, scheduling, and retention efforts to support enrollment goals. · Facilitate informed consent discussions and perform protocol-related study procedures and assessments. · Maintain accurate source documentation, regulatory records, and study files to ensure audit readiness. · Serve as the primary liaison between study participants, sponsors, CROs, and monitoring teams throughout study execution. Qualifications: for the Senior Clinical Research Coordinator include: · 4+ years of experience as a Clinical Research Coordinator supporting industry-sponsored clinical trials. · Demonstrated knowledge of GCP guidelines, protocol implementation, and clinical research regulations. · Experience managing patient-facing research activities, informed consent processes, and study documentation. · Ability to coordinate multiple active studies while maintaining high levels of accuracy and compliance. · Phlebotomy certification preferred; candidates willing to obtain certification after hire are encouraged to apply. · Experience within neurology, psychiatry, or related therapeutic areas is highly preferred. Compensation: for the Senior Clinical Research Coordinator: Salary Range: $80,000-$90,000/year (USD) Comprehensive Benefits: Medical, Dental, Vision, 401(k), PTO, and additional employee wellness programs This job opens for applications on 11/10/2026. Applications for this job will be accepted for at least 30 days from the posting date.