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Reporting to the VP, Clinical Operations, CARGO is seeking a Clinical Trial Associate to play a crucial part in the Study Management Team. The successful candidate will coordinate various administrative aspects of the sponsor's project management and oversight activities.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Serves as the Records Manager for all clinical trials at Corcept throughout the TMF lifecycle (i.e., from study start up to archiving) Working directly with the respective study teams, oversees execution of study TMF plans, ensuring all clinical study documentation is collected, handled, transferred, stored and/or entered into Corcept’s Veeva Vault TMF in compliance with SOPs and global and local standards and requirements.
$170,000 - $180,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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ORA Ph. D. or equivalent doctoral degree in a related field of study such as: Sociology, Business Management, Business Administration, Public Administration, Social Science, Environmental Science, Geosciences, Political Science, Law Enforcement, or other fields related to the petroleum industry.
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This role will help to define and implement meaningful oversight of CROs by supporting study start-up activities, tracking study progress, overseeing the Trial Master File quality and completeness, maintaining meeting agendas and minutes, and implementing learnings/sharing knowledge with other study management teams.
$88,000 - $121,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Strong understanding of science and drug development, with specific expertise in nonclinical study design, preclinical CROs, data management systems, nonclinical study procedures, and statistical analysis methods.
$265,000 - $300,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The successful candidate has experience in drug-development process, clinical study lifecycle, regulatory compliance, and the uses of real world evidence in clinical development and safety endeavors.
$221,170 - $286,220 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Conduct In-Vivo Pharmacokinetic, Pharmacodynamic and Toxicology study design and data review, serving as the main point of contact for receiving, reviewing, and interpreting study data. Experience with In-Vivo Pharmacokinetic, Pharmacodynamic and Toxicology study design and data review.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Oversee and provide strategic direction for Toxicology/Pathology, BioAnalytical/DMPK, Biomarkers, and Clinical Pharmacology teams to ensure robust support for clinical development programs. 12+ years of experience in the biopharma industry in non-clinical development (toxicology, pharmacology, pharmacokinetics, bioanalytical sciences, or related discipline.
$265,000 - $300,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Clinical Data Manager / Senior Clinical Data Manager (CDM) is responsible for data management activities across one or more studies from study start-up through study closure to ensure completion per established project team goals and objectives, including oversight of the CRO DM Vendor, if the project is outsourced.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The senior coordinator will develop, execute, and manage studies funded through NIH, including a study launching in 2024 under a priority precision medicine in mental health initiative. The most direct experience would be with projects using measurements such as neuroimaging within treatment study designs, and with treatment trial designs.
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The Research Assistant will support ongoing research projects that study stem cell and tissue engineering approaches to treat vascular disease and muscle injury. The Research Assistant will support ongoing research projects that study stem cell and tissue engineering approaches to treat vascular disease and muscle injury.
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Responsible for working with regional and country teams to ensure that country and site level Trial Master File is created, maintained and QCd on a regular basis as per the study TMF QC plan. + Accountable for submissions of study in countries in assigned region in close collaboration with regional study start up team and regulatory affairs.
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This position has primary responsibilities for setting strategy across the clinical development program, oversight of strategic study design, study start up, CRO and vendor management, clinical data and safety monitoring, analysis and reporting of studies.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams (e.g., regulatory, translational research,quality, CMC, statistics, etc) in study start-up planning as well as to coordinateefforts for study deliverables (e.g., regulatory submissions, sample reconciliation,PK and exploratory biomarker analyses, SOP development, drug supply projections,pharmacy manual and IP management, developing data cleaning timelines forstats/programming TLF deliverables, etc.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Responsibilities include support the design and execution of multiple clinical studies, proposing novel statistical methodological approaches to enhance study efficacy and sensitivity, and leveraging expertise in Python or R/R-Shiny, Artificial Intelligence, Machine Learning, Deep Learning, RWE, causal inference, etc., as appropriate.
Full-timeExpandApply NowActive JobUpdated 11 days ago
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