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Profoundresearch

Contractor- Clinical Research Coordinator (Oceanside, CA)

Profoundresearch · Oceanside, CA

Posted about 3 months ago

or apply directly on Profoundresearch's site. We never take the application ourselves.

Is this posting real?

This role has been open
80 days
Profoundresearch's roles stay open a median of 81 days
Reposted
No
Salary listed
No
0% of Profoundresearch's roles list one
Ghost-job risk at Profoundresearch
high
14 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
2026-10-24

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 I at Profound Research, you will manage and support high-volume vaccine clinical trials, ensuring efficient participant visits and adherence to protocols. Your responsibilities will include executing clinical procedures, maintaining documentation, and communicating with various stakeholders to facilitate smooth trial operations. This role requires ownership and a strong understanding of clinical research standards, as you will be integral to the success of the trials.

Our read on this posting2.0out of 5
benefits
1/5
freshness
1/5
career value
4/5
role clarity
4/5
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

Worth weighing

  • This is a 1099 contract position, so benefits are not included.
  • The role may convert to full-time based on performance and business needs, but this is not guaranteed.
  • The position requires on-site work, which may involve prolonged periods of sitting, standing, or walking and navigating clinical facilities.
  • Expectations for ownership and independence suggest a fast-paced environment with potentially high demands on time and attention.

Summarised from Profoundresearch's posting. Read the full original.

Listed by Profoundresearch on their lever job board, last confirmed open on 2026-10-24. PitchMeAI is not the employer.

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