What are the responsibilities and job description for the Clinical Trials Project Manager position at RQMIS?
The Clinical Trials Project Manager will develop/implement/ manage all aspects of clinical trials in domestic and international countries for our clients. In addition, the Clinical Trials Project Manager will provide training to clients and internal staff. This is a FULL-TIME salaried position.
OVERALL RESPONSIBILITIES:
- Develop/implement/manage all aspects of clinical trials in domestic and international countries.
- Provide training to clients and internal staff on such areas as clinical trial management, good clinical practices (GCPs), FDA Biomonitoring, CRF design, clinical report writing, Clinical Study Monitoring, etc.
POSITION DUTIES & RESPONSIBILITIES:
- Manage all aspects of clinical projects
- Write departmental procedures and assist in training efforts
- Participate in special projects as needed
- Travel required (up to 30 to 50%)
- Other duties as assigned
EDUCATION & PROFESSIONAL EXPERIENCE:
- Bachelor’s degree in clinical/science field, or similar work experience
- 5 to 7 years of experience in medical device clinical trials
- Previous supervisory or team leadership experience
- Knowledge of domestic/international medical device regulations
- Strong attention to detail
- Strong computer skills, including word processing, spreadsheet, and data programs
- Good oral and written communication skills
- Good leadership skills
- Ability to manage several tasks simultaneously while continuously assessing company and/or departmental priorities
Clinical Trials - Trials Can Pay $1k+
carehealth.com -
Beverly, MA
Clinical Research Site Manager
Alcanza Clinical Research -
Methuen, MA
Community Manager (Andover, MA)
The Mom Project -
Andover, MA