Clinical Research Coordinator

Geneva

  • Bethesda, MD
  • $60,000 per year
  • Permanent
  • Full-time
  • 12 hours ago
About the PositionThe Research Coordinator provides assistance to the Principal Investigator and Study Team coordinating research activities that may include recruiting research participants, data collection and management, and other research activities as assigned. The Research Coordinator will assist with report generation and project close-out support.This is an on-site position assigned to Walter Reed National Military Medical Center and Uniformed Services University in Bethesda, MD. A thorough government background check will be required.About the ProjectJoin the Musculoskeletal Injury Rehabilitation Research for Operational Readiness (MIRROR) team, a collaborative program dedicated to advancing care for musculoskeletal injuries (MSKIs) and reducing their impact on military readiness across the total force. This position will support a diverse portfolio of clinical research studies, including evaluations of platelet-rich plasma (PRP) for knee osteoarthritis, injectable biologics for discogenic low back pain, and ultrasound imaging of the ulnar nerve.Salary Range$60,000. Salaries are determined based on several factors including external market data, internal equity, and the candidate’s related knowledge, skills, and abilities for the position.QUALIFICATIONS
  • Bachelor's 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
  • Comply with all the rules and regulations as applicable to assigned duty station
  • 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
  • Demonstrate proficiency in performing basic study related procedures
  • 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.)

Geneva