Clinical Trials Data Coordinator

Davita Inc.; California (MO); Remote; USD 60,000 - 85,000; Full time

Job summary

A leading healthcare company is seeking a Clinical Trials Data Coordinator for a remote position. This full-time role involves ensuring data integrity across multiple oncology research studies. The ideal candidate will have a Bachelor's degree, along with at least two years of relevant experience, and be well-versed in Good Clinical Practices and federal regulations. Join a dedicated team working to advance clinical research and make a difference in patient lives.

Qualifications

• At least two years of experience related to the conduct of oncology clinical trials.
• Working knowledge of clinical trials and relevant regulations.

Responsibilities

• Ensure data integrity for research studies.
• Coordinate sponsor monitor visits and maintain audit-ready data.
• Oversee electronic research records and patient information.

Skills

Attention to detail

Communication skills

Collaboration

Problem resolution

Education

Bachelor's Degree

Job description

Clinical Trials Data Coordinator - Remote

Join the transformative team atCity 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

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 is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, pleaseclick here.

To learn more about our Comprehensive Benefits, pleaseCLICK HERE.

City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, pleaseclick here.

To learn more about our Comprehensive Benefits, pleaseCLICK HERE.