Clinical Research Coordinator II - Own Your Studies

Profound Research

Carlsbad (CA)

On-site

USD 60,000 - 85,000

Full time

6 days ago
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Benefits offered by this job

Health insurance
PTO
Retirement plan
Professional development support

Job summary

Profound Research is seeking a Clinical Research Coordinator II to serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up to closeout, lead interactions with participants, and maintain audit-ready documentation while collaborating with investigators, sponsors, and CROs.

This on-site role emphasizes owning your studies, ensuring patient safety and data integrity, with opportunities to grow and lead in a dynamic clinical research

Qualifications

  • Bachelor’s degree or higher with 1+ year of relevant experience, OR Associate degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience.
  • Experience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing.
  • Comfortable working independently and managing competing priorities.
  • Strong documentation skills and familiarity with EDC platforms and clinical trial management systems.

Responsibilities

  • Serve as primary coordinator for assigned clinical trials, managing study activities 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 throughout their study experience
  • Maintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
  • Track and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
  • Communicate directly and professionally with investigators, sponsors, CROs, and internal teams
  • Support site readiness for monitoring visits and audits

Skills

Organizational skills
Detail-oriented
Independent worker
Communication

Education

Bachelor’s degree
Associate degree
High school diploma

Tools

EDC platforms
Clinical trial management systems

Job description

Profound Research is seeking a Clinical Research Coordinator II to serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up to closeout, lead interactions with participants, and maintain audit-ready documentation while collaborating with investigators, sponsors, and CROs.

This on-site role emphasizes owning your studies, ensuring patient safety and data integrity, with opportunities to grow and lead in a dynamic clinical research

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