Oncology Clinical Trials Nurse Manager
3 days ago
A Clinical Research Nurse Coordinator at Actalent plays a crucial role in ensuring the successful execution of clinical trials. You will collaborate with investigators to prepare and implement new protocols, screen and enroll study participants, and provide protocol-related clinical management to those participants while on study. The ideal candidate will have two years of oncology nursing experience and one year of clinical research experience.
Responsibilities:
• Collaborate with the Protocol Activation office to initiate and activate new clinical trial protocols
• Prepare and review study tools such as medication diaries and eligibility checklists
• Verify Scientific Review Board (SRB), Institutional Review Board (IRB), data collection plans, and finance/contract approvals prior to study activation
• Translate finalized protocol treatment plans into sample orders
• Serve as a resource for Clinical Trial Billing Information related to assigned studies
Requirements:
• Graduate of an accredited school of nursing with a license to practice in the State of New Jersey
• Bachelor's Degree in Nursing
• Two years of oncology nursing experience required
• One year of clinical research experience
• Proficient in computer applications (Word, Excel, etc.)
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Estimated Salary: $55.00 - $57.00 per hour
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