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Partners closely with the team members from Therapeutic Area, other GCDO functions, Clinical Supply Chain, Bioresearch Quality and Compliance Group, Clinical Business Operations, Finance, Project Management Organization, Regulatory and external partners, to influence alignment on issues and decisions affecting trial management, enabling successful trial outcome.
$117,200 - $263,700 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Partner with Therapeutic Area Heads, Clinical Leads and other functional leaders to optimize the Project Team’s effectiveness and decision making; facilitate team building and communication, create and drive timelines to keep project(s) on schedule.
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Matrix with other parts of the Takeda organizationincludingchemistry, DMPK, safety, translational,and clinical development to advance pipeline programs. Contribute to multiple preclinical or clinical projects, actingas senior scientificconsultant and /orproject team leader.
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In this role, you will represent the Dev DMPK function on cross-functional development project teams; oversee developmental drug disposition metabolism and non-clinical pharmacokinetics activities of multiple projects; be responsible for preparation of regulatory dossier/responses; and assist in developing strategy for the group.
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The Director, Clinical Project Management works cross-functionally with the Epidemiology, Biostatistics, Clinical Informatics, Engineering, and Data Science teams to drive the scoping and execution of new projects.
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As a DPS at Allucent, you will serve as a key role in project administration to ensure delivery of projects within the established budget and timeline in collaboration with Clinical Project Management.
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As a Statistical Project Leader (Associate Director) in our Statistical Innovation Hub, you will provide technical expertise in psychometric analysis to support establishment o novel digital endpoints or re-engineering of existing endpoints from (digital) clinical outcome assessments (COAs.
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Responsible for the validation, nomination and progression of drugdiscovery pipeline programsthroughdirect project championroles and management of junior staff. Scientific leader with deep subject-matter expertise, driving project team progression and development oftechnical capabilities.
$149,100 - $234,300 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Reporting to the Senior Director, Head of Clinical Operations, the Senior Clinical Project Manager/Associate Director will contribute to the overall success of PepGen’s Clinical Development of its Enhanced Delivery Oligonucleotide (EDO) technology.
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As a result of your expertise and efforts we will optimize the use of our clinical trials samples to meet protocol requirements, deliver on our promise to our rare disease patients and advance our science by ensuring our scientists have timely access to all available samples to answer new research questions.
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Clinical Project Director: Harvard Medical School affiliate, Marcus Institute for Aging Research. The ideal candidate has a master’s, doctorate, or advanced clinical degree (nursing or social work) and a minimum of 3-5 years of project coordination or advanced research administrative experience, or equivalent combination of education and experience.
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This includes integrating strategic and tactical input from diverse disciplines (e.g., clinical, regulatory, market access, manufacturing, CMC, commercial, and other areas) as applicable to the project.
$135,500 - $213,400 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago
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