Clinical Research Manager

Overview

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.

Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required.

Bachelor’s degree in biological sciences, health sciences, social sciences or other medical field or equivalent 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.

Requires successful completion of a background check. Selected candidate may be requested to complete a pre-employment physical including a drug screen.

8-12 years of experience in a progressively responsible administrative or management research capacity preferred; supervisory experience preferred; knowledge of clinical trials data mgmt preferred; experience writing research grants and proposals strongly desired.

FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research

CAREER BAND: People Leader
- Managerial

CAREER LEVEL: M2

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Thank you for your interest in working at Ohio State.

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

The university is an equal opportunity employer, including veterans and disability.

• Seniority level:
  Mid-Senior level
• Employment type:
  
  Full-time
• Job function:
  Research, Analyst, and Information Technology
• Industries:
  Hospitals and Health Care

Note:

This description reflects a portion of the position and information provided here is subject to change.