Manager Clinical Research

Cincinnati, Ohio

TriHealth
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Job Overview:

Manager of Clinical Research - Oncology, Medical Specialties and Precision Medicine
The Manager of Cancer Clinical Research is responsible for ensuring TriHealth Cancer & Blood Institute, Medical Specialties Institute and Precision Medicine Institute has an appropriate and well-managed infrastructure for offering clinical research programs to its patients and practicing physicians. -
Responsibilities:

•   Manage and provide accountability for day-to-day operations of clinical research

•   Serve as the primary Sponsor contact for operational project-specific issues and study deliverables

•   Maintain in depth knowledge of protocol, therapeutic area, and indication

•   Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided

•   Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable

•   Develop operational project plans

•   Manage risk assessment and execution

•   Manage study vendors where applicable

•   Manage site quality and monitoring deliverables

•   Develop close working relationships with Physicians, Research Managers and Research Associates

•   Act as an "expert" for many projects managed within TriHealth Cancer & Blood Institute, Medical Specialties Institute, and Precision Medicine Institute.

•   Work collaboratively with the TriHealth Hatton Research Institute.

•   Provide oversight and management to ensure market research initiatives are designed to meet physician and patient needs.

Qualifications -:

•   Bachelor's degree in a health-related field; Advanced degree in a health-related field preferred

•   Experience with Phases 2-3 trials preferred

•   5+ years as a project/clinical research management

•   Management of overall project timelines

•   Strong leadership skills

•   Conducting project kick-off meetings with pharma and cooperative group trials.

•   Responsible for generating as well as maintaining project timelines

•   Creating analysis plans and structure of report deliverables

•   Working with cross-functional teams to coordinate projects from start to finish:

Reporting Structure

•   Reports to Vice President, Clinical Service Lines & Medical Director of Research.

Other Job-Related Information:

Working Conditions:

Climbing - Rarely

Concentrating - Frequently

Continous Learning - Frequently

Hearing: Conversation - Consistently

Hearing: Other Sounds - Frequently

Interpersonal Communication - Consistently

Kneeling - Rarely

Lifting
Date Posted: 07 April 2025
Job Expired - Click here to search for similar jobs