Supervisor Research Operations - Poughkeepsie
Description
Summary: Responsible for overseeing and coordinating the activities of designated clinical research studies. Involves interpreting research protocols, enhancing program initiatives, and maintaining relationships with industry stakeholders, including the FDA and granting agencies. Ensures compliance with Good Clinical Practice and regulatory requirements while leading a team of research staff to achieve departmental goals.
Responsibilities:
1. The Supervisor of Clinical Research is responsible for overseeing and coordinating the activities of designated clinical research studies networkwide
2. This role involves interpreting research protocols, enhancing program initiatives, and maintaining relationships with industry stakeholders, including the FDA and granting agencies .
3. The supervisor ensures compliance with Good Clinical Practice and regulatory requirements while leading a team of research staff to achieve departmental goals .
4. Collaborates with AVP to evaluate new trial opportunities, manage the feasibility committee review through assessments in partnership with clinical teams.
5. Supervises and coordinates the staff and activities of designated studies.
6. Interprets protocols and makes recommendations for program enhancement initiatives.
7. Conducts weekly meetings with the research staff to ensure all research related timelines are maintained, especially with respect to data submission, regulatory submissions and recruitment campaigns.
8. Clinical duties include, conducting protocol specific research tasks within scope of practice (e.g. phlebotomy, EKG, blood pressure, etc.) as well as a limited role in non-research clinical nursing duties as necessary.
9. Hires, trains, disciplines, and evaluates the performance of staff.
10. Maintains comprehensive study lists and cooperative relations with drug companies and research centers .
11. Makes recommendations for program enhancements and best practices.
12. Demonstrates regular, reliable and predictable attendance. Travel to various sites as needed.
13. Performs other duties as required.
14.Maintains and Models Nuvance Health Values.
15.Demonstrates regular, reliable and predictable attendance.
Education and Experience Requirements:
- Bachelor's Degree required, or equivalent combination of education and related experience, plus three years of related experience.
- 4-6 years of relevant experience in clinical research.
- 0-2 years of leadership or management experience.
- Capable of prioritizing and managing several projects at once and taking responsibility for meeting deadlines.
- Prefer: Masters Degree, Registered Nurse (RN) or Licensed Practical Nurse (LPN)
Minimum Knowledge, Skills and Abilities Requirements:
- MS Excel
- Windows
- PowerPoint
- Proven ability to work independently.
License, Registration, or Certification Requirements:
- Certification preferred: Clinical Research Coordinator (ACRP-CP or SoCRA-CCRP) or equivalent experience.
- Current Basic Life Support (BLS) certification.
Salary Range: $40.43 - $75.10 Hourly, commensurate with experience