Research Protocol Analyst - Clinical Research Protections at City Of Hope
Duarte, CA 91009, USA -
Full Time


Start Date

Immediate

Expiry Date

05 Aug, 25

Salary

55.31

Posted On

12 May, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Management System, Microsoft Office, Interpersonal Skills, Processing, Research, Management Software

Industry

Pharmaceuticals

Description

Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we’re changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.
We are looking for a Research Protocol Analyst within the Clinical Research Protections department. They provide administrative, regulatory and operational support to the Cancer Protocol Review and Monitoring Committee (CPRMC), the Protocol Review and Monitoring Committee (PRMC), and the Institutional Review Board (IRB).
You will manage a portfolio of human research protocols from initial submission through the protocol’s life cycle ensuring that protocols are reviewed appropriately by relevant committees. You must be familiar with the human subject protection regulations set forth at 45 CFR 46 and 21 CFR Parts 50, 56, 312, 600 and 812 and other federal guidance, as well as the cancer center support grant requirements.

YOUR QUALIFICATIONS SHOULD INCLUDE:

  • A Bachelors degree with at least 2 years of experience in academic/clinical research review setting. At least 5 years of experience required to substitute for the minimum education requirement.
  • Experience in review and processing of research protocols in an academic research setting
  • Knowledge of complex federal and state regulations involving the use of human and/or animal subjects in research
  • Effective interpersonal skills to deal with complex, sensitive and confidential material with PIs and administrative and research personnel.
  • Certified IRB Professional (CIP) is preferred but not required
  • Software experience related to the role includes Microsoft Office; Outlook Excel; iMedRIS (Committee management software); Forte’s OnCore (clinical research management system)
Responsibilities

Please refer the Job description for details

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