Supervisory Research Health Science Specialist - Research Study Coordinator
Full-time
Others
Asheville, North Carolina
8 months ago
***THIS IS NOT A VIRTUAL POSITION, YOU MUST LIVE WITHIN OR BE WILLING.....
***THIS IS NOT A VIRTUAL POSITION, YOU MUST LIVE WITHIN OR BE WILLING TO RELOCATE WITHIN A COMMUTABLE DISTANCE OF THE DUTY LOCATION***
Supervisory Duties:
- Oversees the daily operations of the unit, ensuring that agency policies and priorities are being followed;
- Develops performance standards and evaluates work performance of subordinates;
- Monitors work efforts and assignments;
- Provides advice, counseling and instruction to employees on both technical and administrative matters;
- Identifies and provides training to staff as needed;
- Hears and resolves minor complaints from employees;
- Effects minor disciplinary measures such as warnings and reprimands;
- Recommends appointments, promotions, and reassignments;
Manages Clinical Tests and Collects Data: - Collects and analyzes data, educates, and interacts with study participants and leadership;
- Provides detailed and summary information and recommendations for further actions based on the data analysis;
- Manages implementation, control and reporting on clinical tests;
- Implements data collection and monitors protocols for difficult clinical research studies;
- Ensures that all tracking data is organized and is monitored during the progress of the study;
- Identifies test results and trends requiring further analysis;
- Maintains all study and regulatory records;
- Prepares project and statistical reports for review process;
Recruits and Manages Candidates for Clinical Trials - Oversees, screens, and evaluates recruitment of candidates for clinical research studies via telephone and/or in person;
- Uses objective rating techniques to identify potential candidates for participation in study where project design is complex;
- Performs informed consent process throughout the study and continuously educates participants on study processes and procedures;
- Performs day-to-day activities related to conducting, overseeing participant interviews and follow-up;
Research Project Support: - Manages the routine, day-to-day activities, and administration of the project;
- Ensures all required documentation, paperwork and forms for initial and continuing human subject's review are submitted by established timeframes;
- Analyzes processes and documentation to ensure compliance with all technical, regulatory requirements, and information safety regulations;
- Conducts quality assurance evaluations for project data and clinical research instruments, as applicable; Establishes and monitors remediation plans to correct deficiencies;
- Drafts detailed and summary reports for presentation at meetings and conferences and for publication in peer reviewed journals;
- Compiles and produces educational and training materials to include determining content needed for training binders and tools;
Performs other directly related duties as assigned.
Work Schedule: Monday through Friday, 8:00am - 4:30pm
Recruitment & Relocation Incentives: Not authorized
Critical Skills Incentive (CSI): Not approved
Financial Disclosure Report: Not Required
Starting at $82,830 Per Year (GS 12)
Official account of Jobstore.