Job Title: 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.