Principal Scientist, - USA - Pennsylvania - North Wales (Upper Gwynedd)

Job Description · Principal Scientist / Director, GLOBAL REGULATORY CMC Biologics (R5) · Under general supervision of an Executive Director/Senior Director, the Principal Scientist /Director is responsible for developing and implementing Chemistry, Manufacturing, and Controls (CM ...

Job Description · GRACS CMC – Principal Scientist, CMC, – Pharm Pre-approval (Inhalation/Respiratory Franchise) · Reporting to the Ex-Director/ Sr. Director in Pre-approval Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our Company ...

A Principal Scientist/Director has primary responsibility for developing value evidence strategies. · Develops American Managed Care Pharmacy (AMCP) dossiers for US payers, · and Global Value Dossiers · , Critically assesses drivers and barriers to reimbursement · , · ...

This position resides within our company's Value and Implementation (V&I), Outcomes Research organization. · Lead or participate in value evidence teams. · Critically assess drivers and barriers to reimbursement. · ...

Under the guidance of a senior leader, a Principal Scientist/Director has primary responsibility for developing value evidence strategies. · ...

This is an exciting opportunity for a Principal Scientist to join our team! As the primary responsibilities of this role include developing the integrated evidence strategy for cardiometabolic products worldwide and planning Outcomes Research and Real World evidence programs. · ...

Job summaryUnder the guidance of a senior leader, a Principal Scientist/Director, has primary responsibility for developing value evidence strategies, · and planning/managing real world and economic evidence activities for in-line · and pipeline products to meet the value eviden ...

Develops value evidence strategies for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers and health systems globally. · ...

The incumbent has primary responsibilities for developing integrated evidence strategies including HTA/reimbursement and overall Real World evidence strategies for cardiometabolic products on a worldwide basis.Develops integrated evidence strategy including HTA/OR strategy genera ...

The incumbent has primary responsibilities for developing the integrated evidence strategy, including HTA/reimbursement and overall Real World evidence strategies. · In-depth understanding of HTA/reimbursement and market access needs in key global markets. · Previous Outcomes Res ...

This position resides within our company's Value and Implementation (V&I), Outcomes Research organization. · ...

The Principal Scientist will develop the integrated evidence strategy for cardiometabolic products on a worldwide basis. · ...

Job Description · Associate Principal Scientist, Regulatory CMC - Biologics (R4) · This Associate Principal Scientist position is equivalent to an Associate Director position. · Under direction from Director/Executive Director, the Assoc Principal Scientist is responsible for imp ...

As part of Our Company s Manufacturing Division, · the Sterile Drug Product Commercialization group provides · the technical process leadership and laboratory capabilities · for late stage and commercial drug product processes for vaccines, · biologics, and sterile pharmaceutical ...

As part of Our Company's Manufacturing Division, the Sterile Drug Product Commercialization group provides technical process leadership and laboratory capabilities for late stage and commercial drug product processes for vaccines biologics and sterile pharmaceutical products. · T ...

Job Description · Role Summary · Under the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence n ...

Job Description · Principal Scientist, Biologics, Sterile Drug Product Commercialization · As part of Our Company's Manufacturing Division, the Sterile Drug Product Commercialization group provides the technical process leadership and laboratory capabilities for late stage and co ...

Job Description · GRACS (Global Regulatory Affairs & Clinical Safety) CMC – Associate Principal Scientist, CMC – Pharm Pre-approval (Respiratory/Inhalation Products) · This Associate Principal Scientist in Pre-approval Pharmaceutical CMC will be responsible for developing and imp ...

In BARDS (Biostatistics and Research Decision Sciences), quantitative scientists apply state-of-the-art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of pati ...

We are seeking a highly skilled Associate Principal Scientist/Associate Director with expertise in conducting outcome researching using real world data. This role requires analyzing complex data sets, developing algorithms, and creating innovative solutions to enhance our data-dr ...