Oct 09, 2019
PARSONS Research Assistant Naval Medical Center Camp Lejeune Parsons is seeking a Research Assistant to support the Clinical Investigations Department (CID) at the Naval Medical Center Camp Lejeune (NMCCL). NMCCL, CID is engaged in the advancement of scholar activity that is operationally relevant to both the Command and the community. CID currently supports a number of research efforts to include traumatic brain injury, post-traumatic stress disorder, alternative treatment therapies, prevention and treatment of mental health disorders and military training and readiness. Responsibilities include: Execute and provide maintenance on research studies. Carry out tasks related to research studies as required by investigators. Maintain files and records of ongoing research projects. Maintain patient confidentiality according to HIPAA and institutional regulations. Make patient appointments by phone and with the use of Composite Health Care System (CHCS) or other method as prescribed by the protocol, command, and clinic structure and assist in the appointment visits. Recruit and telephone screen subjects. Communicate with research subjects; via telephone or in person and ask relevant research questions as per protocol. Perform selected research subject visit duties, for example, presenting questionnaires and collecting demographics. Perform data collection as per protocol and enter data into Microsoft Excel and Statistical Package for the Social Sciences (SPSS) databases (if applicable). Transfer data from questionnaires and data sheets to the databases. Preparation of progress reports and documentation of all correspondence and communication pertinent to the research projects Perform administrative duties related to the research such as obtaining signatures and delivering documents to CID for the investigators. As required by protocol, obtain patient's medical record/reports following procedures. Obtain lab and x-ray results as needed, via CHCS or AHLTA systems. Assist principal investigators, research team members, and other staff in the development of, preparation for, and closeout of clinical research studies. Actively participate in CID departmental and command-wide research educational and training programs by providing instruction, presentations, and assistance to research staff as needed. Assist the compliance Officer with monitoring process to ensure protocol compliance. Attend conference and other meetings as required by the protocol, the PI or sponsoring agency as authorized by the contract. Perform other research related duties as needed and within the scope of work. Education / Experience: Bachelor's Degree with a focus in Biology, Healthcare or related discipline (such as Psychology) OR the equivalency of a minimum of three years working experience in a research setting to include a hospital, physician's office, or academic setting, i.e., pre-med student. A minimum of one year of experience coordinating research protocols as a certified research coordinator; OR certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA). Must be eligible to obtain and maintain, or currently possess Secret clearance. Ready for action? We're looking for the kind of people who see this opportunity and don't hesitate to act. Parsons is a leader in the world of Technical Services and Engineering. We hire people with a broad set of technical skills who have proven experience tackling some of the greatest challenges. Take your next step and apply today.
Professional Diversity Network Camp Lejeune, NC 28547, USA Full-Time