Assists in designing, developing, executing, and implementing scientific research and/or development. Designs, writes, and executes protocols for evaluation of vaccine candidates in small and large animal models. Conducts laboratory assays to assess humoral and cellular immune responses in vaccinated animals. Develops and refines new assays for faster and efficient enumer

Is responsible for the Directorate Protocol program and monitors regulatory approvals for all projects. Also serves as HJF liaison for regulatory oversight. Assists in oversight of the Directorate abstracts and publication processes; interacting with program staff, including assigning and reviewing work, providing guidance, and submitting on government systems. Works with

Oversees and coordinates tasks for the study's various activities. Reviews tasks lists; ensures timely completion of project tasks. 'Prepares and maintains schedule of site visits, leadership briefings, and stakeholder interviews with national child exploitation investigators. Coordinates meetings with US Department of Homeland Security staff members. Uses qualitative res

Develops and coordinates an evidence synthesis program to support systematic, scoping, and related literature reviews across disciplines associated with polytrauma and limb loss. Develop policies and procedures for evidence synthesis in support of EACE strategic goals. Maintains comprehensive knowledge of principles and practices of evidence synthesis, expert searching an

Develops and maintains key internal and external relationships to improve the success of the HJF capture process. Gains clear understanding of customer requirements and assists customer in developing solutions that meet their needs. Champions the solution/opportunity internally to gain cross organizational support and buy in. Serves as key point of contact between the pro

Experience with International clinical trials including vaccines, therapeutics and/or cohort studies for infectious disease indications. Ability to contribute to the development of clinical study designs and clinical protocols. Serve as project/study 'owner' managing all time line, deliverable and fiscal aspects of assigned responsibilities. Serve as primary point of cont

Assists investigators and research staff in the conduct of clinical research studies. Performs a variety of research, data, and clerical duties of a routine and technical nature to support the conduct of clinical research. Assists in the preparation and submission of regulatory documents to the study sponsor and IRB, as required by the protocol and regulatory requirements

1. Independently performs waived, moderate and high complexity testing using manual and automated processes. Complies and participates with all regulatory agency guidelines (CLIA 88,TJC, CAP, FDA, etc.) and addresses concerns as needed. 2. Independently identifies and resolves analytical problems, troubleshoots equipment issues andtakes corrective action in evaluating tes

The Strategy, Policy, Plans and Programs (SP3)division is looking for a Research Scientist to join their team. Staff at this level will typically be leading smaller and/or less complex projects, playing a critical role as a team member on projects with specific regional, functional, and/or technical expertise, or operating as a field rep. Staff will be able to d evelop an

Apply appropriate procedural techniques related to specimen procurement and handling, instrument operation, operator maintenance, application of universal precautions and inventory monitoring. Perform and document quality control procedures and proficiency testing in accordance with established parameters and standards. Accurately enter assay results into client reports R

Under the supervision of the OCT Director, we are seeking a Regulatory Specialist II (RS) who will support investigator(s) and study team(s) in initiating studies. The RS will proactively engage with Principal Investigators (PIs) and their teams upon execution of Non Disclosure Agreements/Confidentiality Disclosure Agreements (NDA/CDAs) to offer assistance with study star

Study Visits (40%) Ensure that research charts are prepared on a timely manner, organized and maintained. Make appointment reminder calls/emails to the study patients. Complete feeding plans for baseline visits with patients. Communicate vehicle for peanut introduction with nutrition. Enter and update appointment information in CRMS, PCRU and EPIC. Data Management (35%) D

The Department of Pediatrics is seeking a full time Research Program Coordinator (RPC) for the division of Endocrine and Diabetes. Under general supervision, the successful candidate will work under two junior faculty pediatric endocrinologists and manage the day to day administration of their research programs. The RPC would spend 50% of their time managing each PI's res

Overall organization of the laboratory and its personnel. Lab related scheduling tasks, such as lab meeting and joint group meeting schedules. Perform scientific assays/experiments relevant to specific projects. Perform preliminary data analysis, summarize results, and report data to the Pl as well as present findings in laboratory meetings. Supervise undergraduate worker

Coordinate and implement recruitment efforts to obtain participants for research studies. Schedule research participants for testing. Participate in running the testing of research participants. Coding behaviors of research participants. Occasional testing of participants in their homes and/or schools. Hire and train undergraduate research assistants. Supervise current un