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Note the following does NOT fit the requirement: management of clinical trials, IT project management, facilities project management or project management within a Pharma company but hasn’t supported development/project management of a new medicine.
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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Conducts medical review and interpretation of efficacy and safety data from clinical trials; this may include delivery of top-line report in collaboration with study statistician, and delivery of clinical study report in collaboration with medical writer and accountable for overall quality and timeliness of analysis and reporting.
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The Director will work closely with senior management and our business development team to gain credibility with our clients by identifying and recommending innovative services and solutions that translates into new business; and successfully delivering our solution engagements in support of our clients in planning and execution of successful clinical trials.
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Experience in the design, execution, and reporting of clinical trials in oncology with small and large molecule drug candidates. SUMMARY/JOB PURPOSE:In collaboration with clinical and project teams of the company, the Clinical Science Director designs, plans and develops studies in early and/or late phase clinical oncology.
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This position reports to the Associate Director, Global Clinical Supplies Quality and is critical to maintaining the global clinical supply chain via disposition activities for clinical finished goods provided by our Company for worldwide clinical trials.
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This position will support the VP, Therapeutic Area Lead in successful execution of clinical trials including engaging appropriately in scientific exchanges around product information, disease education, and research ideas/activities with KOLS, investigators, physicians, and ancillary HCPs regarding current and future therapies in development.
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The Site Director - Philadelphia will be responsible for the execution and oversight of the clinic’s operational functions, inclusive of P&L, and will execute on Flourish Research’s mission of providing high-quality clinical trials to our growing client base utilizing a fiscally responsible, collaborative approach.
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Six or more years of experience in biomarker development and implementation in oncology clinical trials is required. The Associate Director, Biomarker Strategy will have responsibility for developing and effectively implementing biomarker strategies to support the clinical development plans for projects within the Interventional Oncology portfolio.
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IQVIA is a leading provider of scientific services spanning clinical trials, real world evidence, consulting, and technology. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment.
$167,400 - $286,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The Director, Biometrics is responsible for managing the design, monitoring the statistical analysis, and developing tracking systems to determine the efficiency/safety of clinical trials.
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Identify opportunities for leveraging AI and data science across various functions, including drug discovery, clinical trials, manufacturing, commercial operations, and corporate functions, to drive efficiency and innovation.
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DSG has successfully supported over 1,500 clinical trials with innovative, award-winning technology solutions including our flagship software product eCaseLink EDC (Electronic Data Capture), electronic patient diaries, data management,robust reporting and data analysis tools, and digital on-demand CRF publishing software.
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As a Director, Business Development, you will be responsible for generating new and repeat business for ICON Clinical Research, promoting our services throughout the Pharmaceutical, Biotechnology and Medical Device industries.
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Responsible for managing the strategy, design, development, and evaluation of the clinical plans and expediting the implementation of related clinical trials for the purpose of regulatory filing, obtaining outcomes data, and marketing efforts.
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clinical trials director jobs in King Of Prussia, PA
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