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This position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit risk profile throughout product lifecycle.
$92 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Title: Regulatory Studio - Associate Director, Precision Medicine & Digital Health. Worked on drug trials that use a biomarker to select patients into the trial, include but not limited to, understand clinical trial assay (CTA) requirements with diagnostic partners, sample testing/shipping regulations in different countries, and CDx development requirements.
$55 an hourExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Common Job Titles: We frequently fill positions such as Research Scientist, Clinical Research Associate, Quality Assurance Specialist, Regulatory Affairs Manager, Pharmaceutical Sales Representative, and more.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The Associate Director of Regulatory Writing is a key role responsible for producing scientifically accurate, high-quality clinical regulatory documents while adhering to regulatory guidelines.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Specifically, the candidate will support the development and optimization of pre-clinical and clinical assays for neutrophil-mediated diseases by assisting with cell culture, in vitro and ex vivo assays, and molecular biology assays.
$119,267 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Culture primary cells and continuous cell lines such as neutrophils, hematopoietic stem cells, immune cells, and/or relevant cell lines to support in vitro/ex vivo experiments.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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A New Jersey State license to practice as a Psychologist (Psy. D/Ph. D), Licensed Professional Counselor (LPC), Licensed Clinical Social Worker (LCSW), Licensed Associate Counselor (LAC), or Licensed Social Worker (LSW.
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For Associate Director level with Ph. D. approximately 5+ years experience with demonstrated progression clinical pharmacology and Pharmacometrics experience. The CP&P team interacts with discovery and translational scientists, project leadership, early and late clinical development teams and commercial colleagues to provide input on clinical pharmacology profiling, dose optimization, formulation bridging, and combination strategies to enable faster and more effective drug development informed by core scientific principals and data.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The in-house Clinical Research Associate / Senior Clinical Research Associate (CRA) is a key contributor to early phase/clinical pharmacology studies. Strong understanding of ICH/GCP, applicable standards, and FDA regulations for clinical trials.
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The Research Associate II, Formulation Development contributes to the drug discovery and drug product development process by developing and supporting formulations for preclinical and clinical evaluation and performing pre-formulation characterization studies to support drug product formulation development.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.
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Training on ICH/GCP Guidelines & overview of clinical drug development will be provided to all new hires. Engagement Strategy aligned to Diversity and Inclusion in Clinical Trials (DICT.
$109,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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This role responsibilities include: facilitating vendor selection, RFI, RFP, contracting, and negotiation with a focus on CRO services outsourced in support of clinical trials. Has excellent communication skills and is comfortable interacting with internal and external teams, such as, clinical operations, finance, legal, business conduct, vendor management and payments.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Associate Degree required; Bachelor’s degree preferred. Atlantic Health System is seeking a Per Diem Respiratory Therapists for the Morris Plains Clinical Services Unit. The position will be working approximately 2-day shifts per week - 8:30 - 5pm Monday -Friday.
Full-timeExpandApply NowActive JobUpdated 17 days ago
clinical associate jobs in Bernards, NJ
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