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Founded in 1987, Canfield Scientific, Inc. is a core imaging lab providing custom photographic systems, image monitoring, and centralized analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting documentation.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Previous relevant & significant clinical study experience, across the broad spectrum of Clinical Pharmacology and FIH studies, either in the biopharmaceutical industry leading early phase clinical trials, as a PI or sub-investigator in a CRO or relevant academic medical center.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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As a Biostatistician, you will play a key role in analyzing and interpreting data from clinical trials, contributing to the design of study protocols/method validations, and providing statistical insights to support decision-making.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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This role will be responsible for the sourcing, contracting, including, facilitating vendor selection, RFI, RFP, contracting, and qualification with a focus on CRO services outsourced in support of Gilead clinical trials.
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Provide Statistical leadership to oncology clinical trials: developing trial design options and providing high quality decision support. Is expected to oversee and contribute to the completion of all technical and operational statistical activities for a group of clinical trials for a compound/indication or equivalent through management of internal and external resources.
$173,910 - $225,060 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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This role will be responsible for the sourcing, contracting, including, facilitating vendor selection, RFI, RFP, contracting, and qualification with a focus on CRO services outsourced in support of clinical trials.
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This role will be responsible for the sourcing, and contracting, including, facilitating vendor selection, RFI, RFP, contracting, and qualification with a focus on CRO services outsourced in support of clinical trials.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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This position will be responsible to develop and maintain sourcing plans, as well as sourcing events and contracting in a clinical research environment. In-depth knowledge of the clinical research process and the regulatory environment across functions.
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Actalent Clinical Study Specialist Morristown , New Jersey Apply Now 3 IMMEDIATE CLINICAL TRIALS SPECIALIST OPPORTUNITIES IN ONCOLOGY WITH LEADING BIOPHARMA. Summary: The Clinical Trial Specialist/In-house CRA provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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This role will be responsible for the sourcing, contracting, including, facilitating vendor selection, RFI, RFP, contracting, and qualification with a focus on CRO services outsourced in support of Client clinical trials.
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Collaborate with cross-functional teams to design and implement statistical methodologies for clinical trials, including sample size determination, randomization schemes, and statistical analysis plans.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Strategic Relationship Manager provides support and assistance in the planning, execution and management of outsourcing for services associated with global clinical trials. Work with clinical study teams to evaluate outsourcing needs for global clinical trials and assist in developing specifications for contracted deliverables.
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Manages contract and sourcing activities for clinical development programs providing consistent customer service and delivering quantitative value through cost savings and transformation/innovation.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Provide regulatory support and guidance to the technical, medical/clinical team with post marketing CMC changes, labeling and packaging review, and phase IV clinical trials, etc. Provide regulatory support and guidance to the technical, medical/clinical team with post marketing CMC changes, labeling and packaging review, and phase IV clinical trials, etc.
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Responsibilities: Support and maintains clinical data management processes and data capturing systems for clinical trials by following Ferring SOPSupport CRFs development, data mapping specifications, DVP, DMP, and data transfer specifications and tests EDC system functionalities.
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clinical trials jobs in Mine Hill, NJ
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