CLINICAL TRIALS DATA COORD - 10033964

Anywhere, USA

City of Hope is an independent biomedical research and treatment center for cancer, diabetes and other life-threatening diseases.

Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hope’s translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope™, a wholly owned subsidiary, was launched in 2019 and is dedicated to serving employers and their health care partners by providing access to City of Hope’s exceptional cancer expertise.

A National Cancer Institute-designated comprehensive cancer center and a founding member of the National Comprehensive Cancer Network, City of Hope is ranked among the nation’s “Best Hospitals” in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.

Pay Rate: $30.67 - $47.54 per hour

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.

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.

To learn more about our Comprehensive Benefits, pleaseCLICK HERE.

CLINICAL TRIALS DATA COORD - 10033964

Anywhere, USA

Apply now Make a referral

City of Hope is an independent biomedical research and treatment center for cancer, diabetes and other life-threatening diseases.

Pay Rate: $30.67 - $47.54 per hour

Clinical Trials Data Coordinator - Remote

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.

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.

To learn more about our Comprehensive Benefits, pleaseCLICK HERE.

PRINCIPAL CLIN RESEARCH COORD - 10034029

SR CLINICAL TRIALS DATA COORD - 10034024

CASH MANAGEMENT ANALYST - 10034197

SENIOR ELECTRONIC DATA CAPTURE ANALYST - REMOTE - 10033534

SENIOR COMPLIANCE ANALYST, RESEARCH COMPLIANCE - 10033690

CLIN TRIALS MONITOR/ AUDITOR - 10033539

COMPLIANCE ANALYST, RESEARCH COMPLIANCE - 10033682

EXECUTIVE DIRECTOR, STRATEGIC CONTRACTING - 10034158

EXECUTIVE DIRECTOR, PAYER RELATIONS - 10034161