Senior Clinical Research Coordinator: Own Your Studies

Profound Research; Carlsbad (CA); Sur place; USD 85 000 - 110 000; Plein temps

Avantages offerts par ce poste

Health insurance

PTO

Retirement plan

Professional development

Résumé du poste

Profound Research in Carlsbad, CA is seeking a Clinical Research Coordinator III to serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout and interact directly with investigators, sponsors, and CROs to ensure compliant, high-quality data.

You’ll own the study process, maintain audit-ready documentation, oversee patient interactions, and support regulatory and safety reporting to advance patient care and trial

Qualifications

• Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years, OR HS diploma with 4+ years and 1+ year CRC experience.
• Experience performing clinical procedures and data collection.
• Strong documentation and ability to manage competing priorities.

Responsabilités

• Serve as primary coordinator for assigned clinical trials from start-up through closeout.
• Execute full visit flow independently: participant visits, protocol procedures, data collection, and documentation.
• Lead patient interactions with clarity and compassion, ensuring participants feel informed and supported.
• Maintain audit-ready documentation across source documents, CRFs, and EDC systems.
• Track and report adverse events, deviations, and safety findings per protocol.
• Communicate with investigators, sponsors, CROs, and internal teams.
• Support site readiness for monitoring visits and audits.

Connaissances

Clinical research experience

Documentation skills

EDC software

Independent worker

Study coordination

Formation

Bachelor’s degree +1y CRC

Associate’s degree +3y CRC

HS diploma +4y CRC

Outils

Study management systems

Description du poste

Profound Research in Carlsbad, CA is seeking a Clinical Research Coordinator III to serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout and interact directly with investigators, sponsors, and CROs to ensure compliant, high-quality data.

You’ll own the study process, maintain audit-ready documentation, oversee patient interactions, and support regulatory and safety reporting to advance patient care and trial