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The primary role for this Protocol Navigator (PN) position is to provide clinical research regulatory support through the NINDS Clinical Trials Unit (CTU) for the NINDS Intramural Research Program, including specific groups as assigned.
Full-timeExpandUpdated 22 days ago - UpvoteDownvoteShare Job
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Develop novel methodologies for analyzing immunological and pharmacokinetic data from both vaccine and monoclonal antibody clinical trials. Responsibilities Provide accountability for the scientific deliverables and contributions of the Vaccine Research Center’s (VRC) Translational Science Team. Oversee essential team functions, ensuring that: All scientific objectives of VRC clinical trials are met; Clinical trial data is accurately analyzed and project timelines established by VRC leadership are met.
$67,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
$10,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provide leadership and medical expertise in the planning and implementation of CVIsupported vaccine clinical trials and related activities (e.g., epidemiological studies, vaccine preparedness studies, effectiveness studies, post-marketing pharmacovigilance, development and training of key staff, etc.
Full-timeExpandUpdated 27 days ago - UpvoteDownvoteShare Job
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The MEL conducts critical activities that support advancing science, educating on evolving clinical practices, transforming science into patient care, and facilitating the development of new research collaborations (including Investigator Initiated Trials and Real-World Evidence.
Full-timeRemoteExpandUpdated 22 days ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator II conducts and manages multiple clinical trials from start up through study close out in accordance with the study protocol, GCP, and Velocitys SOPs.
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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
Full-timeRemoteExpandUpdated 25 days ago - UpvoteDownvoteShare Job
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
InternExpandUpdated 23 days ago - UpvoteDownvoteShare Job
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Ensure the smooth running of the clinical research program team including that colleagues are updated on all relevant issues, develops systems to track multiple projects including all regulatory files, investigator and IRB information, patient recruitment activity and financial management as well as ensuring high data quality across all clinical trials.
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Serves as a preceptor for new employees, coworkers and students and evaluates their performance by validating clinical and technical skills and interpersonal interactions. Maintains clinical skills specifically required on unit.
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Serves as protocol liaison to community-based physicians regarding patient referrals for clinical trials in coordination with the ACTU Study Coordinator. Ability to learn the clinical trials and/or grants process.
Full-timeExpandUpdated 22 days ago - UpvoteDownvoteShare Job
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Experience with developing study concepts for clinical development and clinical trial designs with cross functional input, including biostatistics, observational research and patient reported outcomes in Phase 2 and/or 3 clinical trials.
Full-timeRemoteExpandUpdated 24 days ago - UpvoteDownvoteShare Job
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5 - 10 years of customer facing Project Manager experience in a SaaS, CTMS, EDC, Patient Recruitment or other Clinical Trials services environment focused on delivering implementations. To be successful in this role, you will need to demonstrate superior product knowledge to effectively collaborate with stakeholders in the research pharmaceutical, biotechnology, and medical device industries who have chosen Vibrent as the platform for their research programs or clinical trials.
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Synthesize project workloads for vaccine and antibody-based development from research through Phase I and Phase I clinical trials. Synthesize project workloads for vaccine and antibody-based development from research through Phase I and Phase I clinical trials.
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EDUCATION, EXPERIENCE AND QUALIFICATIONS · Licensed as a Registered Nurse (RN) or Advanced Practice Registered Nurse (APRN) in the State of Florida. All new to practice RN will be placed into the RN Residency Program.
$15,000 a yearExpandUpdated 22 days ago
clinical trials jobs in Mclean, VA
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