- Bristol Myers Squibb (Princeton, NJ)
- …labeling strategies. + Act as the key PV representative for interactions with global regulatory authorities and stakeholders, advocating for patient safety. + ... benefit-risk assessment, and aggregate safety reporting. + Experience interacting with global regulatory authorities and scientific advisory bodies **Preferred… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …the Global Compliance Operations team and reports directly to the Senior Director , Global Head of Ethics and Compliance Training and Communications. The ... Director will lead the development, implementation, and...compliance training and communications strategy, ensuring alignment with the global objectives, legal and regulatory requirements. +… more
- Integra LifeSciences (Princeton, NJ)
- …standards of care. We are seeking an experienced, strategic, and results-driven Director Executive Compensation that will lead the development, implementation, ... relation to executive compensation alignment, retention strategies, and harmonizing HR policies. ** Global Equity and Incentive Programs:** + Lead the design and… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …or external reviews including ensuring alignment with Gilead business needs and regulatory requirements. + Stay current with evolving global PV regulations ... audits, in the biopharma or related industry. + Proficiency in pharmacovigilance regulatory requirements ( Global ) is a must. + Expert-level experience working… more
- Regeneron Pharmaceuticals (Warren, NJ)
- We are seeking a Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, ... study data of a clinical development program. The Associate Director leads in a matrix environment as part of...day may include the following: + May function as lead Clinical Scientist for program, and/or as delegate of… more
- Bristol Myers Squibb (Princeton, NJ)
- …development including analytical validation, clinical development, manufacturing, US and global regulatory submission, and commercialization of diagnostics. ... medicine and R&D. We have an exciting opportunity for a Senior Director to join the Precision Medicine, Bioanalytical and Translational Sciences organization, where… more
- J&J Family of Companies (New Brunswick, NJ)
- …#: R-029481 + Netherlands (Leiden) Req #: R-029481 **Position Summary** The Sr. Director , Risk Management & External Engagement has oversight for the Regulatory ... design and implementation of an effective and proactive Risk Management & Regulatory Intelligence framework to optimally prepare and support the Innovative Medicine… more
- AbbVie (Florham Park, NJ)
- …will be based on qualifications listed below. Purpose: The Scientific/Medical Director , Medical Affairs provides specialist medical and scientific strategic and ... scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. + Has overall responsibility for oversight… more
- Bristol Myers Squibb (Princeton, NJ)
- …collaborative and high-performance culture. + Drive efforts to ensure enterprise meets global regulatory requirements and legal mandates for Supplier Human ... and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Global Supplier Human Rights, is responsible for implementing… more
- Merck (Rahway, NJ)
- …and lead a cross functional team members to support global commercialization and technology transfer activities and drive product robustness for sustained ... **Job Description** **Job Summary:** The Associate Director of Device Technology is a key leadership role within the Device Development and Technology Organization.… more