Clinical Research Project Manager, Department of Neurology & Rehabilitation
Listed on 2026-06-27
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Science
Clinical Research
Clinical Research Project Manager
The University of Cincinnati, College of Medicine, Department of Neurology and Rehabilitation Medicine is seeking a full-time Clinical Research Project Manager for the NIH-funded Stroke Net Thrombectomy Endovascular Platform (STEP) clinical trial. STEP is a unique, first-of-its-kind platform trial that is looking at various treatments for patients with an Acute Stroke. As the Prime Project Manager of, the candidate will oversee several aspects of national project management for this unique clinical trial.
The project manager will work directly with performance sites in the clinical trial. The appropriate candidate should have a clinical background and extensive clinical research experience.
Essential Functions:
- Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines
- Prepare, oversee, and review documents that are related to the assigned clinical study
- Arrange or help in organizing clinical study meetings
- Ensure the availability of necessary resources for the execution of clinical projects
- Help develop training materials and train clinical staff at sites
- Communicate with sites regarding key study updates during study webinars and other avenues
- Lead the clinical project team and various study team meetings
- Fully involved in resolving issues; take part in procedure improvement initiatives
- Attain clinical study goals by working with other members of the study team to outline their priorities, and to also resolve conflicts that may come up in the project process
- Work hand-in-hand with the study team to manage documents that are related to the clinical study
- Responsible for maintaining the protocol versions and manual of procedures for the trial
- Help prepare safety reports in collaboration with clinical leaders of the project and sites
- Work collaboratively with team members to ensure regulatory compliance
- Perform related duties based on departmental need.
Required
Education:
Bachelor's Degree. Nine (9) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.
Required Experience:
Five (5) years related experience.
Additional Qualifications Considered:
- Excellent communication skills to effectively convey messages across to both study team members and other external people like vendors and external consultants
- Good problem-solving, organizational, and leadership skills are highly required
- Ability to work with little or no supervision
- Ability to pay keen attention to detail at all times
- Must be able to work within stipulated time frames or deadlines even in the face of multiple responsibilities or projects
- Must be able to work as part of a team or in most cases lead a team
- Must have a 'one of a kind' work ethic, and must exhibit a great level of self-discipline
- Ability to organize and motivate other members of the study team
- Proficient user of basic computer applications for the execution of daily project operations
- Experience in writing clinical study procedures and other clinical documents is a plus
- Experience in an academic or clinical setting in the area of clinical specialization
Physical Requirements/Work Environment:
- Sitting
- Continuously - Repetitive hand motion (such as typing) - Often
- Talking
- Often - Hearing, listening
- Often
Compensation and Benefits: UC offers an exceptional benefits package designed to support your well-being, financial security, and work-life balance. Highlights include:
- Salary/Hourly Pay Rate Information
- Comprehensive Tuition Remission
- Robust Retirement Plans
- Real Work-Life Balance
- Additional Benefits Include:
Competitive salary based on experience Comprehensive health coverage (medical, dental, vision, prescription) Flexible spending accounts & wellness programs Professional development & mentorship opportunities
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