Vaccine Clinical Research Coordinator — Impact & Growth

Profound Research

Riverbank (CA)

On-site

USD 55,000 - 85,000

Part time

14 days+

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Benefits offered by this job

Meaningful impact
Professional growth
Leadership potential
Collaborative culture
Full benefits
Clinical exposure variety

Job summary

Profound Research in the United States is seeking a Clinical Research Coordinator I to support high-volume vaccine trials on-site at our California site in Riverbank. You will manage study activities, lead participant visits, and ensure protocol-required procedures and documentation are completed with accuracy.

This 1099 contract role emphasizes ownership, collaboration with investigators, sponsors, CROs, and internal teams, and may convert to full-time based on performance and business needs.

Qualifications

  • Proven clinical research experience and ability to manage study visits.
  • Experience with protocol-driven workflows and source documentation.
  • Ability to perform clinical procedures and maintain accuracy under pressure.
  • Comfortable working independently in a fast-paced site environment.
  • Strong documentation and regulatory knowledge (GCP, GDPr).

Responsibilities

  • Serve as coordinator for assigned vaccine trials from start-up to closeout.
  • Execute visit flow with patient interaction and protocol procedures.
  • Support high-volume clinic days ensuring efficient visit flow.
  • Lead patient interactions with clarity and compassion.
  • Perform procedures such as vital signs, EKGs, phlebotomy, specimens.
  • Maintain audit-ready docs across CRFs, EDC, CTMS, and sources.
  • Communicate with investigators, sponsors, CROs, monitors, and teams.
  • Support site readiness for monitoring visits and audits.
  • Follow GCP, GDP, and infection control expectations.

Skills

Clinical research experience
Communication skills
Attention to detail
Independent work

Education

Bachelor’s degree with 1+ year
Associate’s degree with 3+ years
High school diploma with 4+ years + CRC experience

Tools

EDC platforms
Clinical trial mgmt systems
eSource tools
EMRs
Lab portals

Job description

Profound Research in the United States is seeking a Clinical Research Coordinator I to support high-volume vaccine trials on-site at our California site in Riverbank. You will manage study activities, lead participant visits, and ensure protocol-required procedures and documentation are completed with accuracy.

This 1099 contract role emphasizes ownership, collaboration with investigators, sponsors, CROs, and internal teams, and may convert to full-time based on performance and business needs.

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