Qualifications

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

Responsibilities

Promote safety and confidentiality of research participants at all times

Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (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

Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope

Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives

Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives

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