Clinical Research Specialist II
About The Position
As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. The main functions of this position are to oversee activities within a portfolio of active grant projects across several labs. This involves coordinating projects, activities, personnel, deliverables, and pre- / post-award responsibilities associated with grants (currently HRSA, DoD, NIH). This position will also provide support for intern applications/interviews/onboarding and interface with community medical partners as well as accreditation recordkeeping, reporting, and self-study/site visitations for the Rochester Psychology Internship Consortium (RPIC) based in Addiction Psychiatry. The internship program is a component of grant-related activities. This is a full time position.
Requirements
- Bachelor’s degree required
- 4 years of experience or equivalent combination of education and experience required
- Ability to understand, follow and coordinate standard research protocols and procedures required
- Fully adheres to applicable safety and/or infection control standards required
- Understands and follows data integrity standards and processes required
- Proficient in MS Office (e.g. Word, Excel, and PowerPoint), email, internet preferred
Nice To Haves
- Advanced degree in health systems administration, public health, clinical informatics, or similar preferred
- Strong interpersonal, communication, and organizational skills preferred
- Highly collaborative, ability to work well in teams preferred
Responsibilities
- Participant recruitment, enrollment, and retention: Oversees, coordinates and conducts recruitment of research participants for various active grants at Strong Recovery. Follows up with participants to enhance retention through outreach and participant compensation. Tracks participant payments and compliance with research protocols. Tabling events will be mandatory and may occur on nights and weekends. Actively directs the activities of study staff and clinicians, providing updates to project PIs.
- Project services, advancement, and presentation: Manage upper-level resources, budgets, timelines, clinical trial management, in overseeing grant logistics and service delivery. Function as a main point of contact for funding agencies, community stakeholders, and partners within the university as well as RPIC agencies. Duties include presentation of data and project activities to stakeholders.
- Regulatory: Demonstrates accountability for continuous learning in accordance with Good Clinical Practice guidelines. Keeps current with industry standards, best practices, relevant research studies and designs, implements and monitors resulting study changes.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
