Senior Clinical Research Coordinator

Piper Companies is seeking a Senior Clinical Research Coordinator to join a rapidly growing clinical research organization for a full-time onsite position in Encino, California. The Senior Clinical Research Coordinator will play a key role in overseeing day-to-day clinical trial activities, supporting patient engagement, and ensuring studies are conducted in accordance with sponsor requirements, regulatory standards, and established protocols.

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.

Keywords: clinical research, clinical trials, clinical research coordinator, GCP, regulatory compliance, informed consent, neurology, psychiatry, patient recruitment, study startup, study closeout, source documentation, protocol adherence, sponsor relations, CRO, clinical operations, research compliance, IRB, FDA regulations, ICH guidelines, EDC, CTMS, patient retention, quality assurance, trial management, clinical study coordination, adverse events, clinical documentation, site management, healthcare research, medical research, regulatory documentation, participant enrollment, audit readiness, protocol execution, research records, clinical development, study monitoring, research site operations.

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