Qualifications

Bachelors degree (Advanced degree preferred) or equivalent work experience required

2-4 years experience in 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

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

Prepare research subjects (animal or human) for research study

Execute and maintain research study

Manage study documentation to include accurate and timely filing

Prepare progress reports

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

Procure supplies and equipment as authorized per research budget guidelines

Comply with all the rules and regulations as applicable to assigned duty station

Assist in all phases of the research project to include: recruit research participants, consent volunteers, administer questionnaires, prepare animal research, sanitize animal research areas

Coordinate data collection schedules of all research team members,

Monitor budgets

Create and adhere to a data quality and quality assurance plan

Assist with interim and annual reports. S/he will be the primary liaison at the data collection site and will be responsible for explaining the project to military personnel associated with the study

Make travel arrangements for consultants, when needed

Schedule and attend regular team meetings

Assist with the initial coding and data entry of structured questionnaires and data collection tools, when applicable

Demonstrate proficiency in performing basic study related procedures (i.e., Vital Signs, ECG, phlebotomy, animal surgery) as required

Recruit research participants, assist in enrollment and protocol procedures, monitor follow-up visits, oversee regulatory and administrative details, and provide data management assistance and project close-out support as applicable

Complete required and applicable research training needed to complete research

Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.)