Own Your Studies: Clinical Trial Coordinator

Profound Research; Carlsbad (CA); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

PTO

Retirement plan

Professional development

Job summary

Profound Research is seeking a Clinical Research Coordinator I to join our on-site team in Carlsbad, CA. You will manage study activities from start-up through closeout, lead participant visits, and ensure audit-ready documentation in collaboration with investigators, sponsors, and CROs.

You will own patient interactions, maintain data integrity, and support site readiness for monitoring visits and audits in a fast-paced clinical research environment.

Qualifications

• Strong documentation skills and familiarity with EDC platforms and clinical trial management systems.
• Experience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing.
• Ability to work independently and manage competing priorities.

Responsibilities

• 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 are 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 and regulatory requirements.
• Communicate with investigators, sponsors, CROs, and internal teams.
• Support site readiness for monitoring visits and audits.

Skills

Documentation skills

EDC platforms

Clinical procedures

Independent work

Education

Bachelor’s degree + 1 year experience

Associate’s degree + 3 years experience

High school diploma + 4 years + 1 CRC

Job description

Profound Research is seeking a Clinical Research Coordinator I to join our on-site team in Carlsbad, CA. You will manage study activities from start-up through closeout, lead participant visits, and ensure audit-ready documentation in collaboration with investigators, sponsors, and CROs.

You will own patient interactions, maintain data integrity, and support site readiness for monitoring visits and audits in a fast-paced clinical research environment.