- J&J Family of Companies (Spring House, PA)
- Johnson & Johnson Innovative Medicine is recruiting for a Director , Submission Program Management Leader. This position can be located in Spring House, ... people can reach their potential. At Johnson & Johnson, we all belong. The Director , Submission Program Management Leader (SPML) will be accountable for… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 TAU within ... Management leadership, oversight, direction and planning. + Directly supports program GRL by ensuring project management and regulatory operational support… more
- Penn Medicine (Plainsboro, NJ)
- …day. Are you living your life's work? We are hiring for an Associate Director Oncology Research Operations to join our Cancer Services team at Penn Medicine ... individual must have oncology healthcare research expereince. Summary: + The Associate Director Oncology Research Operations reports directly to the Director of… more
- Taiho Oncology (Princeton, NJ)
- …of data, and authoring/review of scientific and regulatory documents. The Associate Director of Biostatistics will have CRO oversight, management of statistical ... Associate Director , Biostatistics Princeton, NJ, USA Req #421 Monday,...as required (eg, Interim analysis, Meta-analysis etc.) + Keeps management current on project status and provides ongoing risk… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Director Clinical Development - Respiratory Date: Dec 17, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 59023 ... difference, and new people to make a difference with. **The opportunity** Director , Clinical Development is responsible for the development, execution and … more
- SERV Behavioral Health System (Hamilton, NJ)
- …and life satisfaction through a wide range of services. JOB SUMMARY: The Director of Grants and Foundations is responsible for developing and writing persuasive ... Reporting to the Senior Vice President of Development and Marketing, the Director will write, assemble, and submit grant requests; establish and maintain personal… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development ... guidance. **How you will contribute:** With guidance from leadership: Management of Labeling Cross-Functional Teams + Independently leads Labeling cross-functional… more
- Sumitomo Pharma (Trenton, NJ)
- …https://www.us.sumitomo-pharma.com or follow us on LinkedIn. **Job Overview** The Director , Medical Affairs Strategy (Hematology/Oncology) will be a key member ... of the Medical Affairs team reporting to the Executive Director , Medical Affairs Strategy. In this role, individuals are responsible for Medical Affairs strategic… more
- Ascendis Pharma (Princeton, NJ)
- …to working together as one team to achieve extraordinary results. The Associate Director Regulatory Affairs, Advertising and Promotion will be an internal expert on ... the promotion of prescription drug and biologic products. The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing… more
- J&J Family of Companies (Raritan, NJ)
- Johnson & Johnson Innovative Medicine is recruiting for a Director , Global Regulatory Leader. This position can be located in Spring House, PA; Horsham, PA; ... can reach their potential. At Johnson & Johnson, we all belong. The Director , Global Regulatory Leader, is responsible for global regulatory strategies for select… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …in cross-functional drug discovery, development and commercial product lifecycle management and contributes strategic, expert input into scientific and regulatory ... writer to join our dynamic team at the Associate Director level. You will author a wide range of...and as lead medical writer for a large development program or TA. You will participate in or may… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Regulatory Affairs Strategy Princeton, NJ, USA Req #415 Wednesday, November 27, 2024 Looking for a chance to make a meaningful difference in the ... Europe. Position Summary: + Under the direction of regulatory affairs management , the incumbent independently prepares and directs global regulatory affairs… more
- Integra LifeSciences (Princeton, NJ)
- …outcomes and set new standards of care. _Integra Life Sciences is looking for a Director of IT Business Engagement & Process Excellence with a proven track record of ... starting initially with a deep focus on our Compliance Master Plan Program including Quality, Regulatory, Supply Chain Operations, Compliance systems. This role… more
- Bristol Myers Squibb (Princeton, NJ)
- …expertise to cross-functional BMS colleagues + Maintains matrix management responsibilities across internal and external networks **Position Responsibilities** ... support development + Serving as principal functional author for Regulatory submission , study reports, and publications + Provides oversight and medical… more
- Bristol Myers Squibb (Princeton, NJ)
- …regulatory risk, and developing global filing strategies. + Co-lead marketing application submission teams for indications that are at regulatory filing stage to ... liaison input. In collaboration with the Global Regulatory sub-team, develop global submission plans and HA interaction plans. + Provide input into the development… more
- Merck (West Point, PA)
- …process development, qualification, and validation; and design control and risk management techniques to positively support and influence clinical and commercial ... engineering analysis and testing, medical device design controls, risk management , test method/fixture development, design verification and validation, injection… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance of higher level. Reviews and oversee completion ... of trial, clinical trial plan and contingency planning; Analyzes and updates management on potential risks to study deliverables; Provides input on ICF creation;… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …medicine approaches by effectively integrating drug and diagnostic regulatory and submission plans including HA engagement plans and mitigation strategies + Ensures ... line management and key stakeholders are apprised of developments that...long-term disability coverage, basic life insurance, a tuition reimbursement program , paid volunteer time off, company holidays, and well-being… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Myeloma Research Program Manager (Cancer Center) Job Profile Title Manager Research Project B Job ... Teams that support disease/discipline specific cancer programs within the ACC. This Program Manager will have oversight of the ACC CRU- Myeloma Research Team.… more
- Bausch + Lomb (Bridgewater, NJ)
- …leading the advancement of eye health in the future. Reporting to the Senior Director for Insurance & Risk Management , **t** he **Treasury** **Analyst, Insurance ... to ensure proper accruals. + Creates ad-hoc reports and presentations to senior management , as needed. + Supports global surety program including placement and… more