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The RWE Director will closely collaborate with cross-functional partners including Regulatory, Clinical Research, Clinical Operations, Biometrics, Medical Affairs, Patient Advocacy, and Commercial to successfully incorporate HEOR strategies and evidence generation to support the development and commercialization of our asset in acromegaly.
$235,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Cross functional partners include R&D, GSM, US marketing, Business Development, Medical Affairs, Clinical Research, Regional HEMA & Marketing, Regulatory Affairs, HCC and Legal. Advanced degree (MS, MPH, PhD, MHA, MBA) in health economics, outcomes research, or healthcare-related field is required.
$312,110 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Work closely with Global Patient Safety and Risk Management (GPSRM), Clinical Research, Regulatory Affairs, Clinical Operations, Biostatistics, and Medical Affairs to inform clinical development and real-world outcomes and answer product- and disease-area research questions for Alnylam RNAi therapeutics using observational studies, EMR/claims data, and RWE. The Senior Director, Epidemiology reports directly to the Senior Vice President, Data Science, Statistics, and Epidemiology.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Director, Health Economics & Market Access for the Robotics and Interventional Solutions platforms, reporting to the Senior Director, HEMA for Energy/Endomech/Robotics, will work in close collaboration with Global Strategic Marketing, Research & Development, Medical, Clinical & Preclinical, and Regional HEMA partners to build and execute fully integrated health economic and market access strategies for the Robotics and Interventional Solutions platforms.
$312,110 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Johnson & Johnson is recruiting a Director, Health Economics & Market Access (HEMA) for the Johnson & Johnson MedTech Surgery business with a focus on the Robotics and Interventional Solutions platforms.
$312,110 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The Director will support a therapeutic area and cultivate strong partnerships to enable effective cross-functional collaboration with other product team members from internal groups including HEOR-Strategy, Clinical Development and Operations, Biostatistics, Regulatory Affairs, Medical Affairs, and the Commercial organization.
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The Senior Director of Regulatory Affairs and Quality is a hands-on leadership role. 10+ years of relevant regulatory/industry experience in biotech or pharmaceuticals with at least 8 years as the global Regulatory Affairs lead representative on project development teams that have led to marketing authorization.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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With clinical development, regulatory affairs, biostatistics, medical writing, and other stakeholders, lead the development of fit-for-purpose RWE study protocols and statistical analysis plans for approval by internal scientific and strategic forums.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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PhD (preferred), or MS/MPH in epidemiology, biostatistics, health economics and outcomes research, or similar required. This leadership role leads a team of direct reports and drives strategic decision-making to create best in class RWE research to support clinical and regulatory submissions.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Master's or similar degrees in healthcare administration, such as MBA, MHA, MS, MPH, or MPA. Expert knowledge of regulatory environment including Joint Commission, CMS, National Committee for Quality Assurance (NCQA.
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Requires a Bachelor's degree, and a minimum of 12 years prior relevant experience in a managed care healthcare setting with experience in Compliance, HIPAA/Privacy, FWA and/or Regulatory Affairs operations preferred, including 6 years of management experience.
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The Senior Director, Clinical Operations Oversight ensures clinical and operational program integrity and compliance with state and federal regulatory standards and accreditation standards.
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Collaborate with cross-functional teams, including regulatory affairs, quality assurance, and data management, to ensure the successful execution of clinical projects. Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 30 days ago
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