Full-Time

Clinical Research Manager

Clinical Trials Management Office

Posted on 9/2/2025

Ohio State University

Ohio State University

No salary listed

Company Does Not Provide H1B Sponsorship

Columbus, OH, USA

In Person

Category
Biology & Biotech (2)
,
Required Skills
Data Analysis
Requirements
  • Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education 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 and must be maintained.
Responsibilities
  • Serves as Clinical Research Manager in the Department of Neurosurgery; works conjunctively with the COM Center for Clinical Research Management (CCRM); participates in execution of clinical research activities in collaboration with site Principal Investigator(s);
  • Evaluates and implements designated aspects of new research strategies and protocol start-up; participates in developing and implementing processes to enroll patients to clinical trials to ensure consistency and integrity in eligibility determination, recruitment and subject management;
  • Collaborates with the CCRM to implement study participant consenting processes to comply with COM, sponsor and federal regulations;
  • Oversees and manages planning, implementation and execution of clinical trials within the Department of Neurosurgery; plans and supervises daily administrative, research and patient care activities of the clinical research staff;
  • Oversees clinical research staff’s recruitment activity including, interviewing, screening and enrolling of patients into relevant protocols;
  • Assists with training and re-training of newly hired and current clinical research staff; supervises clinical research data collection, management, analysis and reporting;
  • Collaborates with investigators to develop research protocols and assists with writing and preparation of grant applications to obtain research funding; participates in writing and submission of manuscripts and articles for publication and presentation;
  • Conducts quality assurance reviews of research processes and data; ensures compliance to federal, state and local regulations and guidelines; plans, coordinates and participates in site visits by research sponsors and regulatory agencies as needed; actively contributes to the COM and Department research initiatives.
Desired Qualifications
  • 8-12 years of experience in a progressively responsible administrative or management research capacity preferred;
  • Supervisory experience preferred;
  • Knowledge of clinical trials data management preferred;
  • Experience writing research grants and proposals strongly desired.
Ohio State University

Ohio State University

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