Jefferson
Jefferson
Jefferson je zdravstvena in izobraževalna organizacija, ki skrbi za skupnosti na širšem območju Filadelfije, v dolini Lehigh, severovzhodni Pensilvaniji in južnem New Jerseyju. Več kot 65.000 članov njene ekipe podpira izvajanje zdravstvene oskrbe v 32 bolnišničnih kampusih, poleg tega pa organizacija izvaja raziskave in strokovno izobraževanje prek 10 visokih šol in treh šol, ki ponujajo več kot 200 programov za več kot 8.300 študentov. Jefferson prek organizacij Jefferson Health Plans in Health Partners Plans zagotavlja tudi zdravstveno zavarovanje za 360.000 članov ter tako krepi svojo vlogo v regionalnem zdravstvenem sistemu.

Senior Clinical Research Coordinator – Oncology Trials

Support oncology trial regulatory coordination at Jefferson Health, including PRMC and IRB submissions, regulatory files, amendments, and monitoring preparation.

Opis

  • Oversee clinical trial activities under Good Clinical Research Practice (GCP).
  • Manage assigned trial tasks from startup through closeout.
  • Coordinate participant screening, recruitment, enrollment, and consent.
  • Plan feasibility activities and manage study data.
  • Handle biological specimens.
  • Prepare for monitoring visits.
  • Draft regulatory and IRB documentation.
  • Ensure study procedures follow protocols and applicable regulations.
  • Support orientation and training for new staff.
  • Create workflows and training materials.
  • Update standard operating procedures and guidance documents.
  • Take part in work groups.
  • Act as the primary regulatory contact for assigned protocols.
  • Maintain regulatory binders and files, including version control.
  • Coordinate submissions to ancillary committees, including Radiation Safety.
  • Communicate with IRBs and sponsors about regulatory management.
  • Work with study teams and sponsors to finalize documents in response to PRMC and/or IRB recommendations.
  • Prepare and submit study amendments and continuing review applications.
  • Prepare regulatory files for audits and monitoring visits.

Zahteve

  • High school diploma or GED.
  • Five years of experience with a high school diploma or GED and SoCRA, or six years of clinical research experience.
  • Two years of experience with a bachelor’s degree and two years of clinical research experience.
  • One year of experience with a master’s degree and one year of clinical research experience.
  • Knowledge of Good Clinical Research Practice (GCP).
  • Ability to lift and carry 40–50 pounds.
  • Frequent to continuous standing and walking.
  • Ability to perform role-specific physical activities, including kneeling, bending, squatting, and CPR where required.

Ugodnosti

  • Medical insurance, including prescription coverage.
  • Supplemental insurance.
  • Dental insurance.
  • Vision insurance.
  • Life and accidental death and dismemberment insurance.
  • Short- and long-term disability insurance.
  • Flexible spending accounts.
  • Retirement plans.
  • Tuition assistance.
  • Voluntary benefits with access to group insurance rates and discounts.
  • Tuition discounts at Thomas Jefferson University after one year of full-time service or two years of part-time service.