
Clinical Research Project Manager, College of Medicine, Department of Neurology & Rehabilitation
- Cincinnati, OH
- Permanent
- Full-time
- 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. This job description can be changed at any time.
- Bachelor’s Degree.
- Nine (9) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.
- Possess excellent communication skills so as to be able 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 timeframes 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.
- SoCRA and/or ACRP certification.
- Sitting - Continuously
- Competitive salary based on experience
- Comprehensive health coverage (medical, dental, vision, prescription)
- Flexible spending accounts & wellness programs
- Professional development & mentorship opportunities