GENERAL OVERVIEW:
Provides day to day supervision of all activities surrounding the research in the department to ensure compliance with internal and external regulatory agencies.
ESSENTIAL RESPONSIBILITIES:
- Promotes growth and development of research through networking activities with internal and external agencies. Acts as a liaison to facilitate study progress, compliance and enrollment. (30%)
- Evaluates the workload of personnel and study requirements and appropriately distributes responsibilities to staff. Manages the day to day operation of the clinical research department (30%)
- Regularly reviews the trends and rulings of the governing authorities and monitors and ensures departmental compliance for both internal and external agencies. (20%)
- Supports and oversees the orientation, education and evaluation of all departmental research staff members by conducting performance evaluations and maintaining records of employee competencies, mandatory education and required certifications. (10%)
- Oversee the financial aspect of clinical research studies, participates and monitors clinical trials budget processes and provides reports to management. Performs other duties as requested. (10%)
QUALIFICATIONS:Minimum- Bachelor's degree or relevant experience and/or education as determined by the company in lieu of bachelor's degree
- 5 years of clinical research experience
Preferred- Master's degree
- Research Coordinator certification
- Experience in clinical research budgets as well as required computer skills including SPSS, Excel, Word, PowerPoint and electronic data capture reporting
Disclaimer: The job description has been designed to indicate the general nature and essential duties and responsibilities of work performed by employees within this job title. It may not contain a comprehensive inventory of all duties, responsibilities, and qualifications required of employees to do this job.
