Contractor- Clinical Research Coordinator (San Diego, CA)
Profoundresearch · Southern California
Posted 21 days ago
or apply directly on Profoundresearch's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 21 days Profoundresearch's roles stay open a median of 44 days
- Reposted
- No
- Salary listed
- No 0% of Profoundresearch's roles list one
- Ghost-job risk at Profoundresearch
- low 0 stale, 0 reposted of 14 open
- Hiring momentum
- 20 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Profoundresearch's own lever board since 2026-08-04. Full hiring picture for Profoundresearch.
About this role
As a Clinical Research Coordinator at Profound Research, you will manage and execute high-volume vaccine clinical trials, ensuring efficient participant visits and compliance with study protocols. Your responsibilities will include leading patient interactions, performing clinical procedures, maintaining accurate documentation, and collaborating with investigators and sponsors. This role requires a proactive approach and a strong understanding of clinical research standards in a fast-paced environment.
- benefits
- 3/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Profoundresearch as an employer.
What you need
- Bachelor's degree with 1+ year of relevant experience, OR Associate's 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
- Prior experience in clinical research, including exposure to clinical trial coordination, study visits, source documentation, and protocol-driven workflows
- Experience performing or supporting clinical procedures, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, or lab-related workflows
- Comfortable working independently in a fast-paced, site-based clinical research environment
- Ability to support high-volume patient visits while maintaining accuracy, professionalism, and a patient-centered approach
- Strong documentation skills and understanding of audit-ready clinical research standards
Nice to have
- Experience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
- Prior experience serving as a primary or lead coordinator for assigned studies
- Experience with adverse event documentation, protocol deviations, query resolution, monitoring visits, and sponsor/CRO communication
- Active or prior ICH-GCP, IATA, phlebotomy, or related clinical research certifications
- Experience supporting start-up, closeout, or audit/monitoring readiness activities
What you get
- Competitive compensation
- Health insurance
- PTO
- Retirement plan
- Professional development support
Worth weighing
- This is a 1099 contract role with potential for full-time conversion based on performance and business needs.
- The role requires a proactive approach and the ability to work independently in a fast-paced environment, which may not suit everyone.
- No specific salary or hourly rate mentioned in the posting.
Summarised from Profoundresearch's posting. Read the full original.
Listed by Profoundresearch on their lever job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.