Clinical Research Coordinator Position Available In Philadelphia, Pennsylvania

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Clinical Research Coordinator Job Description Join a leading team in the field of oncology, supporting cutting-edge studies backed by prominent pharmaceutical partners. Contribute to high-profile research aimed at improving the diagnosis and treatment of multiple myeloma. Responsibilities Recruit, screen, and enroll subjects into clinical trials. Explain the informed consent process to participants. Document adverse events accurately and promptly. Collect and manage study documents, protocols, regulatory documents, informed consents, case report forms, and source documents. Prepare applications for the Institutional Review Board (IRB). Essential Skills 2+ years of clinical research experience required. Experience with in-hospital clinical research. Proficiency in patient recruitment and consenting processes. Strong knowledge of IRB and human research protection regulations. Effective communication and writing skills. Experience with adverse event reporting. Additional Skills & Qualifications Bachelor’s degree (BA/BS) preferred. Background in oncology and patient care. Familiarity with Good Clinical Practice (GCP) guidelines. Work Environment Work in a dynamic and fast-paced environment that combines office and hospital/outpatient surgery settings. After three months, enjoy a hybrid work model with three days on-site and two days remote each week. Benefit from state-of-the-art equipment and the opportunity to work on prestigious studies with renowned sponsors at one of the most prestigious academic research institutes in the world.