Calendar Management, Case Report Form (CRF), Clinical Medicine, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Conference Management, Data Analysis, Data Collection, File Maintenance, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Leadership, Legal, Maintain Compliance, Medical Records, Medical Research, Medicine, Meeting Minutes, Military, Nonprofit, Organizational Skills, Patient Status Reports, Physical Therapy, Plan Meetings, QoS (Quality of Service), Regulations, Regulatory Compliance, Reporting Skills, Research Protocols, Time Management
- Reviews new patient records and screens patients for eligibility in participation of research protocol.
- Interviews patients for protocols and collects and analyzes appropriate data for recruitment purposes, determine patient commitment and obtains informed consent.
- Educates patients about the research protocol, their roles in the protocols, and any other vital information.
- Collects, organizes, catalogs, disseminates, and maintains appropriate files of current data. Maintains weekly/monthly status reports on all patients.
- Acts as a liaison between patients and clinicians and serves as a resource for the patients.
- Transcribes and resolves queries of data in case report forms (hardcopy or electronic) and prepares documents, under direction of project heads.
- Adheres to legal, professional and ethical codes with respect to confidentiality and privacy. Assures that protocol requirements are achieved within Good Clinical Practices.
- Schedules patients for appointments and visits. Assists with monitoring audits/visits for protocols. Travels from their assigned workplace to support protocols at other sites as needed.
- Provides support to investigators by generating and/or revising Institutional Review Board (IRB) protocols in accordance with requirements imposed by the committees.
- Ensures consent is properly obtained from participants and that documents and data are properly completed, filed, and tracked.
- Assists in arranging meeting, conferences, and visit requests; maintains office calendars and appointment/meeting schedules as appropriate; prepares meeting agendas and minutes as needed.
- Requests, compiles, and analyzes data to develop reports for leadership, sponsors, and regulatory bodies as needed.
- Ensures compliance with all pertinent regulations, guidelines, and policies.
Join the HJF Team!
HJF is seeking a Clinical Research Coordinator II to perform clinical research and patient treatment in conjunction with one or more specified clinical research protocols. Supervised by either a Clinical Site Manager or designee.
This position will be in support of the Extremity Trauma and Amputation Center of Excellence (EACE) at the Naval Medical Center San Diego. The EACE works to advance medical and scientific knowledge through relevant research that will optimize clinical care and quality of life for Service members and Veterans with traumatic extremity injuries and amputations. We are looking for a new team member to assist with a study aimed at improving pain and function in Service members with limb trauma.
The Henry M. Jackson Foundation for the Advancement of Military Medicine (HJF) is a nonprofit organization dedicated to advancing military medicine. We serve military, medical, academic and government clients by administering, managing and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike. Since its founding in 1983, HJF has served as a vital link between the military medical community and its federal and private partners. HJF's support and administrative capabilities allow military medical researchers and clinicians to maintain their scientific focus and accomplish their research goals.
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The Henry M Jackson Foundation for the Advancement of Military Medicine Inc