Oversee and administer research study and associated activities
Assists in project planning, ensuring that established work scope, study protocol and regulatory requirements are followed
Recruit and coordinate research subjects, as appropriate
Serve as principle administration liaison for the project
Oversee and coordinate the provision of administrative and staff services to investigators
Develop and maintain 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; may coordinate the collection and analysis of research data
Document all correspondence and communication pertinent to the research
Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization

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 possess a positive, friendly and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
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