Clinical Trials Data Coord

Responsibilities

Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations

Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information

Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution

Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements

Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work

Benefits

Full-time remote position

Glassdoor

3.5

Cancer research and treatment nonprofit for diabetes and other illnesses.

Duarte, California, USA

http://www.cityofhope.org

Late Stage

Total Funding

$10.3M

Key Investors

California Institute for Regenerative Medicine

2024-05-20

Grant· $5.4M

2022-02-22

Grant· $4.9M

Leadership Team

Nisha Morris

System Senior Vice President, Chief Communications and Marketing Officer

Vanessa Almendro Navarro

SVP, Chief Commercialization Officer

Recent News

Fierce Healthcare

Industry Voices—Why health system CFOs can't budget their way out of coverage disruption

2026-10-11

Morningstar.com

City of Hope Names New Presidents of Cancer Centers in Arizona and Atlanta

2026-10-07

Study Unveils ‘Plug-and-Play’ CAR T Technology Designed to Adapt as Cancer Changes

2026-09-23

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Qualifications

Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations

Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information

Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements

Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work

Bachelor's Degree, relevant experience may substitute for degree

At least two years of experience related to the conduct of oncology clinical trials

Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements

At least two years of experience related to the conduct of oncology clinical trials.

Required skills

Clinical Practice (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, HIPAA regulations, Oncology clinical trials, Clinical trial conduct, Federal, state, and local regulations, Institutional Review Board (IRB) requirements, Clinical Trial Management Systems (CTMS)

Preferred skills

Written and verbal communication

Experience

2+ years