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Research Study Manager
Actalent
An engineering and sciences services and talent solutions firm connecting specialized experts with industry projects.
Oversee oncology research, manage coordinators, ensure compliance, support recruitment.
Communicate services that will support and enable the growth of clinical research, particularly in recruitment, retention, coordination of research, and data management.
Assist doctors in selecting trials and understand screening processes to improve site enrollment.
Partner with physicians to educate and assist them in selecting appropriate studies and explaining feasibility.
Conduct quality assurance audits to ensure compliance with regulatory standards.
Work with research sites to oversee oncology research and ensure compliance with protocols.
Supervise and manage the workflow of coordinators in the assigned disease-specific group.
What you bring
oncology
supervisory
bachelor’s
clinical research
nci
regulatory
3-5 years of oncology experience.
At least 1 year of supervisory experience.
Bachelor’s Degree in a science discipline.
Experience as a Clinical Research Supervisor or Research Program Manager.
Familiarity with NCI Designated Cancer Institutes.
Strong understanding of clinical operations and regulatory compliance.
Experience in supervising coordinators and managing workflow.
Prior experience in oncology and as a Clinical Research Coordinator (CRC).
Benefits
Time Off/Leave (PTO, Vacation or Sick Leave)
Health Spending Account (HSA)
Employee Assistance Program
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Transportation benefits
Critical Illness, Accident, and Hospital
Medical, dental & vision
Short and long-term disability
401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
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