Oversees and administers research study and associated activities
Assists in project planning, and ensures that pre-established work scope, study protocol and regulatory requirements are followed
May recruit and coordinate research subjects, as appropriate
Serves as principle administration liaison for the project
Oversees and coordinates the provision of administrative and staff services to investigators
Develops and maintains record keeping systems and procedures
Promote safety and confidentiality of research participants at all times
Adhere to OSHA, GCP, GLP, and infection control procedures
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
Plan, implement and maintain data collection and analysis systems in support of research protocol
Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate
Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol
Organize and facilitate meetings, conferences, and other events associated with research activities

Bachelors degree or equivalent work experience required
2-4 years experience in clinical research preferred
2-4 years non-profit, research, or healthcare experience desired
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor
Must be flexible with changing priorities
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Knowledge of CFR, GCP and ICH guidelines

Clinical Research Coordinator

Key skills