Clinical Trials Data Coord

["united States-California-Duarte"]mid

OtherClinical

2 views0 saves0 applied

Apply Now

Quick Summary

Key Responsibilities

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

Requirements Summary

Bachelor’s Degree, relevant experience may substitute for degree. At least two years of exp

Technical Tools

OtherClinical

Clinical Trials Data Coordinator - Remote

Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today.

This full-time remote position entails ensuring data integrity for various research studies. Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data. You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research.

As a successful candidate, you will:

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.

Qualifications - External

Your qualifications should include:

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.