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Effectively motivate team member to lead cross functionally, particularly across Market Access, HEOR, Brand, Government affairs, and Advocacy, to ensure alignment around delivery against access goals at each stage of a products lifecycle.
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This role involves collaboration with various departments, including operations, procurement, legal, research and development, regulatory affairs, and quality assurance to ensure that contracts align with business objectives, comply with relevant regulations, and mitigate risks.
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Work closely with the Data Governance Lead to develop and maintain a right size data catalog of and data lineage for commercial and medical affairs applications. For the expansion of our Business Information Systems (BIS) team, argenx is looking for a Data Architecture Lead with focus on the Commercial and Medical Affairs functions.
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Collaborate with other departments, such as the Business Office, Development and Alumni Relations, the President's Office, Academic Affairs, and the Business Office, to ensure that all student organization events are planned and executed successfully.
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Ph. D. with over 10 years of experience in pharmaceutical regulatory affairs, of relevant experience in biotech or pharmaceutical industries. Provide strategic and operational leadership in regulatory affairs, including regulatory strategies, clinical study requirements, and marketing approvals in various regions.
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The Associate Director is accountable for aligning pre- and post-launch plans with internal constituents in Medical Affairs, Commercial, and Clinical Development Teams. Leading planning, prioritization, and execution in alignment with internal stakeholders (US Medical Affairs, Commercial, Clinical Development) to ensure adequate resources for Medical Review for product launches.
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With a focus on providing talent for field/inside sales, medical device support, clinical support, and medical affairs, our CSMS division has 10,000+ field professionals in more than 30 countries addressing physician and patient needs.
$90,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Collaborate across all internal and external stakeholders (i.e., Market Access Strategy, Contract Operations, GtN, Accounting/Finance, US Public Affairs, Legal, Audit, Commercial leaders, and external Legal and consultants.
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Through a comprehensive understanding of the diagnostic and care landscape, the candidate will closely collaborate with the International Business Unit (IBU) marketing and medical teams, Government Affairs, and International Communication teams to execute, in partnership with the local affiliate teams, integrated solutions designed to remove obstacles to optimal patient pathways.
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Work collaboratively with other Medical Directors, and colleagues in Biostatistics, Medical Writing, Drug Safety, Clinical Operations, Translational Medicine, and Regulatory Affairs. Collaborate with Regulatory Affairs to align studies with local, national and international health authority requirements.
$324,000 a yearFull-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Subject matter expertise in matters pertaining to behavioral threat assessment, both international and domestic (U.S.) affairs, and violent extremism as they pertain to the current threat environment.
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This role includes the management and oversight of the planning, forecasting, packaging, labeling, distribution and return of clinical supplies for assigned clinical trials and collaborates closely with the broader CMC and Supply Chain Management team, as well as with key internal stakeholders such as Clinical Operations, Regulatory Affairs and Quality Assurance.
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Successful candidates would be expected to have demonstrated the potential for excellence in any discipline relevant to international affairs, and share a commitment to the Pardee School’s institutional values of diversity, equity, inclusion, and social justice.
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Work with Community and Legislative Affairs to conduct community engagement with external stakeholders on fare policy decisions. Minimum Qualifications:Bachelor's degree from an accredited institution in public policy, public administration, political science, urban planning, urban studies, or related field.
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This role will develop strong relationships, collaborate, and interact with various departments (i.e., Quality Operations, Quality Systems, Chemistry Manufacturing, and Controls (CMC), Analytical, Regulatory Affairs, Pharmacovigilance, Procurement), and all levels of management at Akebia to accomplish company objectives.
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affairs job Company: Dow in Cambridge, MA
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