- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Regulatory Affairs...degree in Pharmacy, Biology, Chemistry, or other related life science + Minimum 7 years of experience in the ... difference with. **How you'll spend your day** As the Associate Director , Regulatory Affairs you...(MS/PhD in pharmacy, biology, chemistry, pharmacology or related life science , MBA, or MD) + Minimum 10 years of… more
- Abbott (Abbott Park, IL)
- …regulatory data is maintained in electronic systems. + Depending on specific role, the Associate Director Regulatory Affairs may be involved in various ... generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Associate Director of Regulatory Affairs** **About Abbott** Abbott is… more
- AbbVie (Irvine, CA)
- …https://global.allerganaesthetics.com/. Follow Allergan Aesthetics on LinkedIn. Job Description The Associate Director of Regulatory Innovation supports ... of global submissions. Directs and supports development of the regulatory strategy with a focus on Clinical Outcome Assessment...objectives . + Qualifications + Bachelor's Degree in life sciences or engineering . Relevant advanced degree in a… more
- AbbVie (Chicago, IL)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , RA Global Regulatory Strategy, US & Canada ... product within a Therapeutic Area and supports the Global Regulatory Lead (GRL, Director ), in the development...Experience may determine level of position. Senior Manager or Associate Director . Additional Information Applicable only to… more
- AbbVie (North Chicago, IL)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , RA Global Regulatory Strategy, US & Canada ... driver indications for a product within a Therapeutic Area and supports the Global Regulatory Lead (GRL, Director ), in the development & execution of the … more
- Bristol Myers Squibb (Madison, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The role of Associate Director of US Commercial Regulatory Affairs requires ... the ability to apply complex scientific and expert regulatory advice and risk assessment for the development of...single vision as inspiring as "Transforming patients' lives through science (TM) ", every BMS employee plays an integral… more
- Sanofi Group (Cambridge, MA)
- About the Role The Associate Director , US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the ... promotion of prescription drugs and biologics. Essential Functions + Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional brand and… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …their aspirations. Join Gilead and help create possible, together. **Job Description** Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within ... Gilead's Global Regulatory Affairs organization and acts as a critical strategic...the United States:** As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment… more
- Bausch Health (Philadelphia, PA)
- …mission of improving people's lives with our health care products. he Associate Director , Advertising and Promotion, Prescription Drug Products, reviews, ... product advertising and promotional labeling pieces for compliance with regulatory agency requirements. **KEY ACTIVITIES/RESPONSIBILITIES:** + Provides regulatory… more
- BD (Becton, Dickinson and Company) (Milpitas, CA)
- …with us. **Key responsibilities will include:** + Responsible for the global regulatory strategy for BDB products. + Coordinates and advises the preparation of ... complex regulatory submissions, including Premarket (510(k)) Notifications, de novo applications,...degree required with a master's degree preferred in health science or life science field (biomedical engineering,… more
- Boehringer Ingelheim (Ridgefield, CT)
- …labeling. Participate in Human Pharmaceutical Review Committee, providing regulatory opinion on promotional communications. Review scientific exchange communications ... Identify and routinely monitor reliable sources from which to obtain product and/or regulatory information. + Review and signature of FDA forms 2253 with approved… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
- Kelly Services (Gaithersburg, MD)
- Description: The Labelling Strategy Associate Director provides regulatory labelling expertise, typically for more complex drug projects, to the Global ... Regulatory Submission Team (GRST)/Global Regulatory Execution Team...(eg FDA, EMA). Minimum requirements: * University Degree in Science or related discipline * 3 to 5 years… more
- Sanofi Group (Bridgewater, NJ)
- The Associate Director RA serves as the regulatory lead on Review Committees (RCs). As the RC RA representative, work with brands on competitively ... of prescription drugs, biologics, and devices. **ESSENTIAL FUNCTIONS** + Provide regulatory leadership and guidance to Commercial teams during the development,… more
- Novo Nordisk (Plainsboro, NJ)
- … regulatory agencies. Supervise designated personnel. Relationships Report to the Director / Associate Director /Lead Regulatory Scientist/Sr. Manager ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...Position Manage and oversee all assigned projects/products/processes. Assist the Director / Associate Director in assuring Novo… more
- Takeda Pharmaceuticals (Lexington, MA)
- …product responsibilities. As part of the US Medical team, you will report to the Associate Director , Ad/Promo Regulatory Review. You will be based in either ... Join Takeda as a Senior Manager, US Medical Ad/Promo Regulatory Review where you will serve as an internal...you bring to Takeda:** * Bachelor's Degree in life science or equivalent. Advanced degree (PharmD, PhD, MS, MBA,… more
- Sanofi Group (Bridgewater, NJ)
- …the job** **Our team** The team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages and post marketing to ... a later diagnosis. **Main responsibilities:** + Leads the US regulatory post-marketing activities. + As a key member of...PhD, MD or DVM or MSc in Biology, Life Science , or related field) preferred **Experience/Professional requirements:** + US… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Sciences ...and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a ... on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences ....Business partners). + Effectively manage to ensure compliance with regulatory submissions and internal timelines. + Participate in audit… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …focus on creating inclusion, developing talent, and enabling teams. **Job Description** The Associate Director of Global Marketing - Multiple Myeloma (MM) will ... Anito-cel global brand strategy, launch plans, and global marketing deliverables. The Associate Director works in close collaboration with Arcellx marketing and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** **Key Responsibilities** Associate Director , Global External Manufacturing Biologics ensures ... external contract manufacturing network, while ensuring compliance with cGMP, regulatory requirements, and environmental, health, and safety legislations. This… more