Oncology Clinical Research Coordinator - Trial Activation

Temple Health; Philadelphia (Philadelphia County); On-site; USD 55,000 - 85,000; Full time

Job summary

Temple Health is seeking a Clinical Research Coordinator to support the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. The role involves coordinating clinical research protocols to ensure recruitment, safety, and data quality, while developing tools for accrual monitoring and timely study activations.

The position requires a Bachelor's degree with 2+ years of healthcare experience (oncology/clinical trials

Qualifications

• Bachelor's Degree required.
• Graduate level classes or degree in a relevant program preferred or
• Combination of relevant education and experience may be considered in lieu of degree.
• 2 years direct experience in a healthcare setting preferably oncology or clinical trials or a minimum of 3 Years related experience Required
• General Experience and knowledge of chemotherapy and/or radiation therapy administration Preferred
• General Experience Previous experience performing phlebotomy and specimen processing Preferred
• Cert Clin Research Coordinator Preferred Or Cert Clin Research Prof Preferred or

Responsibilities

• Coordinate and facilitate the conduct of clinical research protocols to ensure participant recruitment and accrual, protocol compliance, safety and data quality.
• Develop effective tools for close monitoring and reporting of trial accrual and coordinate timely study activation and protocol amendments.
• Interact with institutional investigators, healthcare team members, service line members and research participants to support conduct of clinical trials.

Education

Bachelor's Degree

Graduate level classes or degree in a relevant program

Job description

Temple Health is seeking a Clinical Research Coordinator to support the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. The role involves coordinating clinical research protocols to ensure recruitment, safety, and data quality, while developing tools for accrual monitoring and timely study activations.

The position requires a Bachelor's degree with 2+ years of healthcare experience (oncology/clinical trials