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Learn More Here - The Project Manager will play a key role in supporting new product development & innovation projects within the new Business Transformation Office (BTO). The BTO has a combined focus on strategic projects, innovation projects, and mergers & acquisition projects supporting JMCRS (JAX Mice and Clinical Research Services) as well as JAX organizational growth.
$84,300 - $141,138ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with industry cross-collaboration amongst functions involved in product launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.
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Economic modeling studies ; familiarity with COA/PRO development, validation research and clinical trial implementation. Independently identifies appropriate internal and external data resources and external experts to execute strategies and research activities led by HEOR.
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Outcomes Research projects. health economics, health services research, pharmaceutical sciences , or related discipline. Experience in drafting of study reports, creation of presentation materials from study reports, ability to present scientific research to non-scientific audiences.
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Scientific Research Annual Plan ; communicates any changes from plan in timely manner. for their potential to affect current research responsibilities in order to provide advice/guidance on best course of action.
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Assures alignment of research activities with. clinical trial design. Actively participates in cross-functional meetings (e.g., Pipeline Commercialization Model teams, Global Brand Teams) as subject matter expert for tactical discussions and proactively escalates foreseeable challenges/issues back to manager in a timely manner.
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Broad multidisciplinary understanding of the pharmaceutical clinical research and development processes with hands on regulatory, clinical operations, or clinical trial monitoring/management experience, e.g., clinical study design, conduct, management, reporting, and/or product development life cycle.
$120,000 - $155,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Within product development and management across the full product life cycle: pre-clinical research and development; clinical development; regulatory submissions and compliance; commercialization; product management; quality assurance and control.
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Lead product development projects and programs in the pharmaceutical, medical technology and biotechnology industries, including pre-clinical R&D, commercialization and product lifecycle management.
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Within each sector we lead, at the core team level, product development projects including pre-clinical R&D through commercialization, including planning for regulatory, clinical, and commercial strategies and processes, and product lifecycle management.
$135,000 - $180,000 a yearFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Within each sector we lead, at the core team level, product development projects from pre-clinical R&D through commercialization, including planning for regulatory, clinical, and commercial strategies and processes, and product lifecycle management.
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Under the supervision of the manager to support the Value Proposition to Regulators, Payers, Patients, Prescribers, and Policy-makers. under the supervision of the manager, to support. Ability to write study protocols with a high scientific standard and able to defend the protocol methodologies at the HEOR Protocol Review Committee review meetings.
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As a service, product, functional and/or therapeutic area Specialist acting as the primary Sponsor/Client project liaison and advocate is responsible to plan, execute, manage, and monitor complex, multinational clinical research project(s), for multiple modalities or in different therapeutic areas.
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The project coordinator for the cardiovascular franchise will work closely with the cross functional teams to plan and execute a variety of ongoing projects across clinical studies, research and development and product management.
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Carry out numerous and varied activities associated with the conduct and successful performance of clinical trials/studies with demonstrated expertise and ability to navigate in at least one project/contract-specific tool or system in support of the following: patient recruitment; data management, collection and processing of adverse events reports; tracking and reporting of site monitoring/management activities, and/or regulatory document collection (e.g., EDC, CTMS, or eTMF systems.
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clinical research product development jobs Title: project manager
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