Clinical Research Jobs in the United States
Guidehouse
$65000 - $78000 Per year
Bethesda, MD
A certification in any of the following: Association of Clinical Research Professionals Certified Professional (ACRP-CP), Association of Clinical Research Professionals (ACRP), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Associate (CCRA) preferred. 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.
Joslin Diabetes Center
Boston, MA
Requests sponsor authorization as necessary on changes in principal investigator, scope or work, key personnel, key personnel effort, performance site, proposed funding period or no-cost extension requests via eRA Commons. Skill in prioritizing workload to complete work in a timely manner where there are pressures of deadlines, competing requirements, and fluctuating workloads, without sacrificing quality.
Guidehouse
Rockville, MD
Work collaboratively with Clinical Trials Operations and Biostatistics (CTOBB) staff, Principal Investigators (PIs), Clinical Coordinators, Government Project Officers (GPOs) and Institute Contracting Officers; advise CTOBB regarding the findings of on-site observation of activities of both the Clinical Trials Coordinating Centers and/or the Clinical sites. Maintain current knowledge of regulatory monitoring literature as well as the design and implementation of scientific studies; read current literature; participating in meetings, conferences, and workshops.
DCS Corporation
Dayton, OH
The NIBS team is responsible for conducting human subject experiments to assess the ability of novel neuromodulation strategies to improve cognition under operationally relevant stressors such as sleep deprivation, physical fatigue, and high workload. DCS Air and Space Technology Sector is seeking a Cognitive Neuroscientist to support our Non-Invasive Brain Stimulation (NIBS) team’s current research efforts.
Joulé
Carnegie, PA
Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes. A top-ranked research university is currently searching for a Clinical Research Coordinator for one of its growing departments to be responsible for assisting in the operations of ongoing clinical trials.
UIC Ophthalmology & Visual Sciences
Chicago, IL
Clinical Research Coordinator within the Ophthalmic Clinical Trials and Translational Center (OCTTC) is responsible for managing, coordinating, and implementing all components of clinical research protocols, including pre and post-research activities both within and outside the clinical setting. Act as liaison between physicians, clinical staff and the UIC IRB office, grant sponsors and regulatory agencies to ensure priorities are clearly communicated and resources are allocated appropriately across multiple ongoing projects.
Judge Group
$140000 - $180000 Per year
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Expertise in clinical trials: a working understanding of statistical principles, demonstrated ability to perform literature research, analyze and author clinical trial publications; thorough knowledge of the whole processes of clinical trials, clinical research concepts, practices, and GCP and ICH Guidelines. Develops the study protocol synopsis, leads the analysis of benefit/risk for clinical development protocols and the final study protocol validation and protocol amendments; supports the clinical operations team during feasibility and study execution.
Judge Group
$105000 - $140000 Per year
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The ideal candidate will have a strong background in clinical research (preferably in Psychiatry), exceptional problem-solving skills, and the ability to build strong relationships with site staff and stakeholders. Perform site troubleshooting and issue spotting, proactively identifying and resolving challenges to ensure the smooth progress of clinical trials.
Judge Group
$325000 - $360000 Per year
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They will lead clinical development strategy and program execution of research projects, and lead translation of pre-clinical observations into clinical experiments and studies designed to demonstrate proof of pharmacology, proof of mechanism and proof of concept for new candidate medicines. They will establishes and cultivates collegial relationships with key clinical experts, academic entities, and clinical trial sites, and uses these relationships to help establish collaborations and enhance the company’s medial/scientific reputation.