Clinical Research Coordinator (Oncology) Job at Medasource, San Luis Obispo, CA

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  • Medasource
  • San Luis Obispo, CA

Job Description

Job Description

Position: Clinical Research Coordinator (Oncology)

Duration: 6-month Contract to Hire

Location: Onsite - San Luis Obispo & St. Marie, California

About the Role:

We are seeking an experienced Clinical Research Coordinator (CRC) to support active oncology clinical trials at hospital-based research sites in California. This is a hands-on, fully onsite role supporting patient-facing research activities from study start-up through close-out.

This is a net-new, urgent opening with a strong likelihood of extension and potential conversion to a full-time role.

What You'll Be Doing:

  • Coordinate and execute oncology clinical trials under the direction of Principal Investigators
  • Recruit, screen, consent, and enroll research participants
  • Coordinate and conduct protocol-required visits, procedures, labs, and assessments
  • Collect, enter, and report study data per protocol and sponsor requirements
  • Process, handle, and ship biological specimens in accordance with federal regulations
  • Support study drug accountability and coordinate medication administration
  • Identify and report adverse events, SAEs, protocol deviations, and violations
  • Participate in sponsor monitoring visits, audits, and inspections
  • Serve as a liaison between patients, investigators, sponsors, IRBs, and clinical teams
  • Maintain inspection and audit readiness across studies

Required Qualifications:

  • 3+ years of experience as a Clinical Research Coordinator
  • At least 1 year of oncology clinical trial experience
  • Experience serving as primary CRC on multiple drug and/or device trials
  • Strong patient-facing experience in a healthcare or research setting
  • Bachelor’s degree in a science or related field (or equivalent experience)
  • Experience with EDC systems and CTMS platforms
  • Ability and willingness to work fully onsite

Certifications:

Willingness to obtain one of the following within 12 months:

  • CCRP (SOCRA)
  • CCRC (ACRP or SCRA)
  • Certified Phlebotomy Technician (ANCC)

Additional Details:

  • Full-time, onsite schedule
  • Equipment provided
  • EHR: Cerner
  • Interview process includes one virtual interview and one onsite interview

Job Tags

Full time, Contract work,

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