- Merck & Co. (North Wales, PA)
- Job DescriptionThe Director , Regulatory Affairs Liaison, is responsible for development and implementation of global regulatory strategy for their ... regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (Rahway, NJ)
- …a critical role in leading major global initiatives aimed at enhancing Medical Affairs practices. The SRO is a recognized internal management consulting team within ... with cross functional teams across multiple geographies and functions.Exposure to Medical Affairs function within a reputed Pharma would be a plusStrong strategic… more
- Aequor (Newbury Park, CA)
- This will be a 100% remote role. The hiring manager confirmed they are looking for someone who works regular hours (7a-4p or 8am-5p etc)/ with EST timezone ... Support the implementation of Veeva Vault, IDMP, EU CTR, and other regulatory initiatives. Work with stakeholders to gather requirements and develop solutions.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Serve on Local Labeling Committee (LLC) and provide medical input to Regulatory Affairs Physical Requirements 30% overnight travel required. Position can ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...Area in certain instances, at the discretion of Executive Director of Medical Affairs . Assists the Senior… more
- Jazz Pharmaceuticals (Palo Alto, CA)
- …please visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter. Brief Description:The Associate Director , Regulatory Affairs will be a key ... efforts to obtain worldwide approvals to market our products. An Associate Director , Regulatory Affairs within the Regulatory Strategy group will… more
- Merck & Co. (Rockville, MD)
- …with the company's Research Laboratories divisions and most directly with Global Regulatory Affairs and Clinical Safety (GRACS) to define and implement ... Research and Development Division's colleagues, regulatory liaison staff, and local regulatory affairs staff for submission of product applications and other… more
- Merck & Co. (Rahway, NJ)
- …there are important interactions with, inter alia, Quality Assurance, Finance, Regulatory , Clinical Supplies and legal in a highly matrix-based organization. There ... are some interfaces with Human Health/Global Medical Affairs (GMA).Primary activities:Provide Leadership to the country(ies): Build the best team and chart the… more
- Jazz Pharmaceuticals (Philadelphia, PA)
- …new ways to solve problems. Collaborate with Biostatistics [clinical and medical affairs ], data science, regulatory , clinical development, medical writing, and ... countries. For more information, please visit and follow @JazzPharma on Twitter. The Director will be responsible for managing the product leaders and external FSP… more
- Jazz Pharmaceuticals (Philadelphia, PA)
- …new ways to solve problems.Collaborate with Biostatistics [clinical and medical affairs ], data science, regulatory , clinical development, medical writing, and ... visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter. Brief Description: The Director will be responsible for managing the product leaders and… more
- Jazz Pharmaceuticals (Philadelphia, PA)
- …new ways to solve problems. Collaborate with Biostatistics [clinical and medical affairs ], data science, regulatory , clinical development, medical writing, and ... information, please visit and follow @JazzPharma on Twitter. Brief Description: The Director will be responsible for managing the product leaders and external FSP… more
- Merck & Co. (Washington, DC)
- … will monitor, analyze, and communicate internally about federal legislative and regulatory activities and initiatives.- The Associate Director will also ... Job DescriptionPosition Description: Associate Director , Federal Policy and Government Relations The Associate Director is responsible for helping to craft and… more
- Merck & Co. (North Wales, PA)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.-Specifically, the Director may be… more
- Merck & Co. (North Wales, PA)
- Job DescriptionPosition Description: Legal Director (FDA promotion/Labeling Drugs & Vaccines) The position provides legal support to the Human Health Division, with ... Act complianceAdvertising and promotionProduct labelingClinical research activitiesCommercial and Medical Affairs policies and practicesPolicy initiatives in support of business… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … Liasions to ensure successful implementation of CDx and data collection- Supports Regulatory affairs in providing content and providing review of documents ... Creates a forward-looking Diagnostic development strategy while keeping abreast of regulatory and policy updates in the external environment and by tracking… more
- Jazz Pharmaceuticals (Palo Alto, CA)
- …area of focus. The Medical Science Liaison team in conjunction with the Director , Medical Science Liaisons and Regional Medical Director , will integrate their ... requires close alignment with the internal stakeholders including Medical Affairs , Commercial, Marketing and Clinical Development groupsEducate payers (Health plans,… more
- DivIHN Integration Inc (Chicago, IL)
- …duration with extension potential (up to 3-4 yrs) Primary Job Function: Supports Global Director of Medical and Scientific Affairs to defining medical affairs ... Divya | 224 369 2969 Title: Medical Manager Location: Remote role but need local to Illinois Duration: 11...the following responsibilities under the supervision of the Global Director of Medical and Scientific affairs : Functions… more
- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May… 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 ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be… more
- Lundbeck (MA)
- …with cross-functional teams.ESSENTIAL FUNCTIONS:STRATEGIC LEADERSHIP Partner with National Director to execute Field Medical strategies, set clear priorities ... scientific knowledge, tools, and communication skills In collaboration with National Director , set individual and team performance goals for MSLs, and continuously… more
- Battelle Memorial Institute (MA)
- …common. Healthcare innovation is at the core of what we do. Join Battelle as the Regulatory Affairs Director where you will lead and drive the organization's ... regulatory affairs strategy for our Health Business...operations in **_Columbus, OH; Boston, MA_** but may be remote . **Major Responsibilities** + Direct all regulatory … more
