Oncology Clinical Trials Lead Coordinator

Temple Health

Philadelphia (Philadelphia County)

Vor Ort

USD 60.000 - 90.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Temple Health is seeking a Clinical Research Coordinator to coordinate and manage clinical research protocols across oncology trials. You will work with the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses to recruit participants and ensure protocol compliance and data integrity.

RESPONSIBILITIES include coordinating trial activation and amendments, interacting with investigators and healthcare teams, and

Qualifikationen

  • 2 years direct experience in a healthcare setting preferably oncology or clinical trials required.
  • General experience and knowledge of chemotherapy and/or radiation therapy administration preferred.
  • Phlebotomy and specimen processing experience preferred.

Aufgaben

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

Kenntnisse

Healthcare experience
Clinical trials

Ausbildung

Bachelor's degree required
Graduate level coursework preferred

Jobbeschreibung

Temple Health is seeking a Clinical Research Coordinator to coordinate and manage clinical research protocols across oncology trials. You will work with the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses to recruit participants and ensure protocol compliance and data integrity.

RESPONSIBILITIES include coordinating trial activation and amendments, interacting with investigators and healthcare teams, and

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