Clinical Research Manager

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Job Title:

Clinical Research Manager

Department:

Medicine | Radiation Oncology

Clinical Research Manager who will manage, develop, and oversee the conduct of non-therapeutic clinical trials for the Department of Radiation Oncology research team under direction of the Chair, Dr. Arnab Chakravarti.

 

Responsibilities:

• Oversees planning, organization, implementation, and execution of all clinical research projects specific to radiation oncology

• Manages and supervises daily administrative, operational, research and patient care activities in a specific cancer disease site collaborating and communicating with faculty, administration, research staff and shared resources within James Cancer Hospital and OSUCCC as appropriate

• Plans, directs, assigns, and monitors team workflow, activities, and productivity to ensure fulfillment of research goals

• Manages hiring, supervising, training, scheduling, and evaluating research personnel

• Directly manages own team of clinical research staff

• Develops and implements plans to meet requirements of new studies/protocols and ensures all requirements within disease team are met

• Plans and leads disease team meetings at which protocol activity and progress, resource allocations and productivity benchmarks are reviewed

• Provides feasibility assessments

• Conducts quality assurance reviews of research processes and data

• Collaborates with OSUCCC investigators in the development, review, submission, and implementation of research protocols

• On a limited level, collaborates with principal investigator (PI) to develop, negotiate, implement, and administer research study budgets

• Reviews, monitors, and approves expenditures to ensure appropriateness

• Manages and supervises recruitment, interviews, screening and enrolling of patients into research protocols

• Develops, implements, and oversees education of patients participating in study

• Ensures appropriate patient care and follow-up according to protocol

• Participates in writing and submission of manuscripts

Minimum Education and Experience:

• Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required

• 5 yrs. experience in a clinical research capacity conducting & implementing research projects required

• Experience in a progressively responsible administrative or management research capacity preferred

• Knowledge of clinical research regulations, guidelines & compliance issues required including Institutional Review Board (IRB) & federal or industry sponsor processes and requirements

• ACRP (Assn of Clinical Research Professionals) or SOCRA (Society of Clinical Research Associates) certification required

• Supervisory experience preferred

• Knowledge of clinical trials data management preferred

• Requires successful com