Sr. Research Program Supervisor (Oncology)
Core
Oversee day-to-day activities of clinical research studies, supervise support staff, and ensure compliance with protocols and regulations.
Role type
Senior Clinical Research Program Supervisor
Builds
Clinical trials and studies for disease prevention and treatment
Domain
Oncology / Clinical Research
Deliverable
client delivery
Required skills
Protocol operational oversight, staff supervision and performance management, budget formulation, regulatory compliance, data collection system setup, recruitment strategy development, IRB submission preparation, literature search, data abstraction
Preferred skills
None stated
Technologies
None stated
Responsibilities
Assist Principal Investigator in ensuring operational feasibility of study design, facilitate administrative hiring processes, oversee day-to-day activities of support staff, delegate and oversee performance of study tasks, set performance goals and conduct evaluations, develop standard operating procedures and data collection forms, develop consent forms for clinical trials, prepare materials for IRB submission, ensure compliance with protocols and regulations, contribute to study budget development, develop and oversee participant recruitment strategy, set up data collection systems, perform self-audits and audit other sites, participate in study meetings and provide status updates, conduct literature searches, abstract and index information
Seniority
Senior, hands-on IC