- Merck & Co. (North Wales, PA)
- Job DescriptionThe Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy for ... point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and...the application or hiring process. We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse… more
- Merck & Co. (North Wales, PA)
- …and approval of all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional ... practices are consistent with regulatory guidelines, our company's policies, and support business objectives.Serve...the application or hiring process. We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse… more
- Merck & Co. (Rahway, NJ)
- …updated on emerging regulations and industry trends affecting device quality and regulatory affairs .Strategic ContributionsServe as a key member of the device ... and Skills:10+ years of experience in device quality, device regulatory affairs , or a related field within...the application or hiring process. We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse… more
- Merck & Co. (North Wales, PA)
- …divestment and product withdrawal.Support new technology development.Demonstrate an understanding of regulatory affairs and applies this understanding to the ... for developing and implementing Chemistry, Manufacturing, and Controls (CMC) regulatory strategies for our organization's biologics product franchises in accordance… more
- Merck & Co. (North Wales, PA)
- …operates under the guidance of the Associate Director who supports the Global Regulatory Affairs & Clinical Safety (GRACS) and Quality Assurance (QA) ... utilization to achieve this mission. This is a unique opportunity to gain exposure and contribute to the Research...analytical support to our Research & Development Division, Global Regulatory Affairs & Clinical Safety (GRACS), and… more
- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding… more
- Merck & Co. (South San Francisco, CA)
- …research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations ).Provide clinical pharmacology ... Operations , Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout research… more
- Merck & Co. (Rahway, NJ)
- …Work effectively with cross-functional partners including research and development, medical affairs , regulatory affairs , manufacturing, Business Development ... & Licensing, market analytics, international and domestic operations , legal, scientific communications, professional education, training and development, health care… more
- Merck & Co. (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Senior Clinical Director May… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …technologies/ Implementing strategic and tactical plans to drive sustainable improvements.Supports Regulatory Affairs in providing quality content and review of ... at key governance meetings whereby GCLP/GLP activities are being discussed ( Regulatory affairs , Research unit LT, GRDC etc.,) Effectively interacts… more
- Merck & Co. (Rahway, NJ)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding… more
- Merck & Co. (Boston, MA)
- …discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations ) for the design and ... Job DescriptionWe have an exciting opportunity for a physician-scientist to join our group as a- Principal Scientist (Clinical Director) in Translational… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Health Systems Oncology Medical Affairs Director (HSO MAD) is a therapeutic and disease expert who develops ongoing professional relationships ... in a balanced and credible manner consistent with the regulatory environment and company's ethical standards. This role also...role also serves as a resource for the Medical Affairs (MA) management team on strategic planning and provides… more
- Merck & Co. (North Wales, PA)
- …people with cancer across the globe.The Regional Associate Director of Medical Affairs - Gastrointestinal Cancer (RADMA) position is a core function within Oncology ... Medical Affairs and supports the achievement of our scientific and...and Skills: Experience with US healthcare treatment guidelines and regulatory process - Experience working in the pharmaceutical industry,… more
- Merck & Co. (Rahway, NJ)
- …assay development and validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of ... the application or hiring process. We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse...Hiring Ordinance Search Firm Representatives Please Read Carefully-Merck & Co ., Inc., Rahway, NJ, USA, also known as Merck… more
- Merck & Co. (North Wales, PA)
- …therapy in Pulmonary Arterial Hypertension (PAH). This role offers a unique opportunity to drive innovation and make a significant impact on patient lives. ... US Brand Marketing, Account Management, Outcomes Research, Policy, and Medical Affairs , to ensure sustainable access and success.Key Responsibilities: Lead a… more
- Merck & Co. (North Wales, PA)
- …incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates and may ... reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs.In… more
- Merck & Co. (North Wales, PA)
- …and resources to address the opportunities.Collaborating with Global Medical and Scientific Affairs (GMSA), US, Senior Director of Medical Affairs (SDMA), Center ... other company brands for a One Company approach.Collaborating with Program Leads, Medical Affairs and Global Expert Management & Strategy to plan for Group Input… more
- Merck & Co. (Rahway, NJ)
- …the Company's vaccines pipeline, including during late-stage development, distribution and regulatory milestones, in a manner that reflects the Company's purpose and ... manage all communications across the vaccine portfolio and pipeline, including regulatory approvals, governing bodies, publications of scientific data and other… more
- Merck (Philadelphia, PA)
- **Job Description** The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy ... point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and...the application or hiring process. We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse… more
