- Genmab (Trenton, NJ)
- …our expanding US Medical Affairs (USMA) team, Genmab is seeking a Senior Director , USMA Solid Tumor Portfolio. This role will report to the VP/Head of US Medical ... generation strategy development and execution of Phase 3b/4 Medical Affairs led interventional and observational clinical trials; Ensures US market needs are… more
- Genmab (Mercerville, NJ)
- …this role will include stakeholders in the business domains Field Operations, Medical & Regulatory Affairs and US Market and Commercial Teams (and others) and ... is essential to fulfilling our purpose. Job Description - Director , Digital Assets, Information Security Position Summary The ...Genmab Security Operations Team Business leaders (eg, VP Medical Affairs , VP Regulatory Affairs , GM… more
- Genmab (Groveville, NJ)
- …patient advocacy groups) internal stakeholders (eg Research, Translation Medicine, Safety, Regulatory , Global Medical Affairs and Commercial) and internal ... continues to grow and is currently seeking a Medical Director to join our Medical Solid Tumor Team, focusing...review and communication of data, and medical input into regulatory documents, and presentations. This position reports to the… more
- Genmab (Mercerville, NJ)
- …advisory boards, patient advocacy groups), internal stakeholders (eg, Research, Safety, Regulatory , Medical Affairs , Commercial), and internal decision boards ... to fulfilling our purpose. The Role: The Senior Medical Director supports Oncology Clinical Devlopment. Responsibilities: Oversee clinical program including… more
- Sun Pharma (Taro Pharma) (Princeton, NJ)
- Senior Director , Global Regulatory Affairs Strategy The position will provide regulatory affairs strategic leadership for the company and novel ... the individual will be responsible for developing and executing the overall regulatory strategy , which includes developing the registration pathway, interacting… more
- Genmab (Yardley, PA)
- …looking for an experienced and passionate leader to be a part of our Global Regulatory Affairs (GRA) organization. In this role, the regulatory leader will ... programs. Importantly, the chosen candidate will manage and mentor a group of Regulatory Affairs strategists. As a key member of the Regulatory Affairs… more
- Genmab (Yardley, PA)
- …for an experienced and passionate leader to be a part of our Global Regulatory Affairs (GRA) organization. In this role, you will be primarily responsible ... our hybrid policy. This position will report to the Regulatory Strategy Team Lead. Responsibilities: The key...Minimum of 5-8 years of hands-on industry experience within Regulatory Affairs (Oncology and/or immunology and inflammation… more
- Genmab (Yardley, PA)
- …and diverse antibody products in immuno-oncology and beyond. Reporting to the Global Medical Affairs Strategy Lead (MASL) the Director will be responsible ... will work as an integral part of the Medical Affairs Strategy Team in close alignment with...on development programs In depth understanding of compliance and regulatory requirements for pharmaceutical Medical Affairs , R&D… more
- Genmab (Yardley, PA)
- …and ensure development and execution of the overall independent medical education grants strategy and operations across Genmab therapeutic areas and to serve as lead ... funded sponsorship opportunities. Role will lead the execution of the Medical Affairs grant and corporate funding system and processes; design and execute strategic… more
- Genmab (Yardley, PA)
- …pipeline product (oncology) in alignment with brand strategies, medical affairs strategies, clinical development plans, support product value propositions, and ... and value for commercial/market access needs. support clinical development, regulatory and safety needs (real world evidence and epidemiology studies).… more
- Genmab (Princeton, NJ)
- … Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to ... Strong business acumen and ability to see the business drivers outside of Regulatory Affairs . Excellent communication skills; both oral and written Demonstrated… more
- Sun Pharma (Taro Pharma) (Princeton, NJ)
- Title | Role: Director , Professional Relations - Specialty Dermatology Sun Pharmaceutical Industries, Ltd. (Sun Pharma) is the fourth largest specialty generic ... is bound by our common values:Humility. Integrity. Passion. Innovation.Job Summary:The Director , Professional Relations - Specialty Dermatology is a key member of… more
- Sun Pharma (Taro Pharma) (Princeton, NJ)
- …(including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations)Provide ... Senior Director of Translational Medicine and Clinical Pharmacology Sun...sciences, preclinical development groups, toxicology, clinical operations, drug metabolism, regulatory affairs , and late-stage clinical research Qualifications:… more
- Genmab (Princeton, NJ)
- …and close communication/interaction with internal eg Data management, biostatistics, regulatory affairs , non-clinical, medical and other functional areas ... be part of the Development Operations Leadership Team who defines the overall strategy and identify development areas of the organization and ensures that all teams… more
- Genmab (Princeton, NJ)
- … precedence, and clinical study designs that deliver value. Partner with Medical, Commercial, Regulatory , and Medical Affairs leaders on the CDT to problem solve ... be our best, and authentic is essential to fulfilling our purpose. Senior Director , Global Program Leader Genmab is seeking an experienced Global Program Leader… more
- Genmab (Princeton, NJ)
- …and authentic is essential to fulfilling our purpose. The Role The Associate Director will support the medical communications strategy and deliverables for ... of medical communications content. This role will report to the Senior Director of Medical Communications and Publications within Global Medical Affairs .… more
- Genmab (Princeton, NJ)
- …our purpose. The Role & Department The Feasibility Lead supports the vision and strategy set forth by the Head of Strategic Feasibility. Advances this effort through ... Partners with key stakeholders within Global Development Operations (GDO), Medical Affairs , Medical, and/or CROs, to enable expedited, predictive delivery for all… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Regulatory Affairs Strategy Pleasanton, CA, USA * Princeton, NJ, USA Req #374 Friday, June 28, 2024 Looking for a chance to make a ... and/or development regulatory activities under the direction of Regulatory Affairs management. The incumbent plans, directs and executes the regulatory… more
- Novo Nordisk (Princeton, NJ)
- …for a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will provide strategic ... Establish strong and positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion. Essential… more
- Ascendis Pharma (Princeton, NJ)
- The Regulatory Affairs (RA) Associate Director , Labeling will be responsible for labeling activities across programs and stages of development, with specific ... labeling, and for coordinating internal labelling activities and processes for regulatory submissions and product maintenance. The Associate Director prioritizes… more
