Principal Clinical Research Coordinator

4 weeks ago

Irvine, United States City of Hope Full time

Principal Clinical Research Coordinator - Orange County

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.

Embark on a rewarding journey as a Principal Clinical Research Coordinator in Orange County, where you'll serve as a key link to the Executive Director of Clinical Research. Within our Clinical Trial Office (CTO), you'll collaborate closely with COH investigators, overseeing a diverse range of research studies involving human subjects. As a PCRC, you'll not only lead your disease team but also provide invaluable mentorship to new staff members, ensuring the seamless integrity of multiple research endeavors. Your adeptness in maintaining data integrity and navigating regulatory landscapes, including GCP, FDA, NIH, and HIPAA, will be instrumental in driving the success of our projects. With a focus on managing complexity, meeting deadlines, and fostering open communication, you'll play a pivotal role in advancing clinical research within our dynamic environment. Don't miss this opportunity to contribute to impactful research initiatives - apply now and become an integral part of our dedicated team

As a successful candidate, you will:

* Ensure protocol procedures are followed as specified
* Report adverse events according to protocol and regulations
* Abstract and enter data accurately and timely
* Ensure data integrity and compliance with GCP
* Liaise with sponsors and attend meetings
* Participate in monitoring visits and audits
* Mentor colleagues and assist in training
* Lead coordination of meetings and study communications
* Participate in meetings and professional development
* Serve as a resource for assigned protocols

Your qualifications should include:

* Bachelor's Degree
* Minimum of five years of experience related to the management and conduct of clinical trials in an academic setting.
* Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development.

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

To learn more about our Comprehensive Benefits, please CLICK HERE.

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