Clinical Research Coordinator Job at Medasource, San Luis Obispo, CA

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  • Medasource
  • San Luis Obispo, CA

Job Description

Location: San Luis Obispo, CA (Onsite)

Employment Type: Contract-to-Hire (CTH)

Start Date: ASAP – End of February 2025

Position Overview

We are seeking an experienced Clinical Research Coordinator (CRC) to join our team in San Luis Obispo, CA , to support oncology clinical trials . The ideal candidate will have extensive experience in coordinating drug or device trials , interacting with patients in a healthcare setting, and ensuring compliance with research protocols and regulatory requirements.

Compensation

  • Non-RN CRC: ~$35-40/hr
  • RN CRC: ~$55-60/hr

Key Responsibilities

  • Coordinate and participate in site initiation visits and sponsor-required training.
  • Recruit, screen, and enroll research participants, ensuring informed consent processes are followed.
  • Coordinate all study-required visits, procedures, and tests according to protocol.
  • Collect, process, and ship laboratory specimens following federal biologics shipping regulations.
  • Maintain accurate data collection and reporting in compliance with protocols, sponsors, and regulatory requirements.
  • Ensure adherence to FDA, OHRP, GCP, and IRB regulations.
  • Monitor adverse events and report deviations, violations, or exceptions to sponsors and IRBs.
  • Prepare and maintain regulatory documents , including IRB applications, informed consent forms, and protocol amendments.
  • Act as a liaison between participants, investigators, sponsors, IRBs, and other stakeholders.
  • Assist in sponsor monitoring visits, audits, and query resolution .

Minimum Qualifications (Hard Requirements)

  • 3+ years of experience conducting oncology clinical trials .
  • Served as primary research coordinator for at least 5 drug or device trials .
  • 3+ years of experience interacting with patients in a healthcare setting .
  • SOCRA (CCRP) or ACRP (CCRC) certification required .
  • Local to San Luis Obispo, CA (onsite role).
  • Bachelor’s degree in a science or health-related field OR equivalent experience.
  • Experience with electronic data capture software and Clinical Trial Management Systems (CTMS) .
  • Lab processing experience required; Phlebotomy certification preferred .
  • Human Subjects Protection & Good Clinical Practice training required .

Preferred Qualifications

  • Experience in drug accountability and specimen collection .
  • Knowledge of oncology research protocols and IRB regulatory processes .
  • Ability to perform blood draws, ECGs, and NIH Stroke Scale assessments .
  • Strong communication and patient advocacy skills .
  • Experience working in a hospital, clinic, or research institute setting .

Interview Process

  1. 30-minute phone interview
  2. Virtual interview with the research team (if moving forward).

Next Steps

  • Ensure candidates have not applied internally before submission (RTR required).
  • Confirm willingness to work onsite in San Luis Obispo

Job Tags

Contract work, Local area, Immediate start,

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