Clinical Research Project Manager, Department of Neurology & Rehabilitation, STEP
- 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
- Repetitive hand motion (such as typing) - Often
- Talking - Often
- Hearing, listening - Often
- 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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