Clinical Research Manager - CCC | Clinical Trials Office

The Ohio State UniversityColumbus, OH

About The Position

Clinical Research Manager to manage, develop, and oversee the conduct of clinical trials of a cancer disease-specific research team within OSUCCC Clinical Trials Office (CTO) under direction of Clinical Trials Director.

Requirements

  • 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
  • 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

Nice To Haves

  • experience in a progressively responsible administrative or management research capacity preferred
  • supervisory experience preferred
  • knowledge of clinical trials data management preferred

Responsibilities

  • Oversees planning, organization, implementation, and execution of all clinical research projects specific to disease team
  • 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
  • Assists Clinical Trials Director in 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 and regulatory staff 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

Benefits

  • Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
  • Paid time off, including sick and vacation time and 11 holidays.
  • State retirement plan or an alternative retirement plan, both with generous employer contributions.
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