Job Title:
Clinical Research Manager
Job ID:
445495
Location:
College of Medicine
Department:
Endo, Diabetes & Metabolism
Full/Part Time:
Full-Time
Regular/Temporary:
Regular
Shift:
Shift Varies
FTE %:
100
Salary Range Min:
$55,390.40
Salary Range Max:
$85,987.20

Position summary

Clinical Research Manager (Job Opening 445495) - Clinical Research Manager who directs the clinical research program in the Department of Internal Medicine in the Division of Endocrinology/Diabetes/Metabolism; reporting to the CTMO Assistant Director and the Operations and Implementation Director, the Clinical Research Manager?s responsibilities are guided by the overall strategic direction set forth by the leadership team of the College of Medicine and the CTMO; oversees planning, organization, implementation and execution of all clinical research projects; ensures compliance with all local, state and national regulations including adherence to Good Clinical Practices (GCP); recruits, hires, trains, supervises and evaluates clinical research staff; plans, directs, assigns and monitors clinical research staff activities and productivity; participates in the development of new projects and protocols; oversees and supervises submission of required regulatory documents; directs, oversees and monitors clinical subject accrual; monitors, identifies and reports adverse reactions of participants; directs and supervises clinical research data collection, management, analysis and report functions; collaborates with Principal Investigators (PI) to develop and negotiate research study budgets with sponsors; implements, administers and oversees grants, budgets and expenditures; assists with the writing and preparation of grant proposals for extramural funding; participates in writing and submission of manuscripts, articles, abstracts and research reports for publication and presentation; develops, implements and oversees collaborative research initiatives; travels to investigator meetings; assists with modifications of project data collection tools to develop information systems and measures to protect patient confidentiality; serves as a liaison with institutional review board (IRB), federal, state and industry sponsors related to patient care issues and patient status; plans, coordinates, oversees and prepares for external

Education and experience

Master?s degree in biological sciences or an equivalent combination of education and experience required; extensive experience in a clinical research capacity conducting clinical research studies required; experience in an administrative capacity working on clinical research studies or in a medical research setting required; clinical research certification from SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) required; knowledge of clinical research regulations, guidelines & compliance issues required; requires successful completion of background check; qualified candidates may be asked to complete a pre-employment physical, including a drug screen.