- Daiichi Sankyo, Inc. (Bernards, NJ)
- …management. Review contribute to revision of DSI contracts (eg development, license , distribution agreements)Manage, negotiate, and revise collaborative license ... Development, Research Development, Regulatory Affairs. Facilitate operational meetings with CROs, License Partners, and PV vendors. Provide PV oversight of the DSI… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …deviations from CCDS; Ensures implementation of CCDS/labeling agreements with licensing partners.Conduct Label Review Committee Meetings: Prepares documents for ... review by labeling teams. Leads review processes and ensures appropriate governance for US, EU and Company Core documents as well as for the review of country labeling deviations.Ensure Compliance with Labeling Regulations and Guidance: Researches applicable… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …KOL interactions on a program based need; Involvement with in- licensing and acquisitions on individual due diligence activitiesQualifications: Successful candidates ... will be able to meet the qualifications below with or without a reasonable accommodation.Education Qualifications (from an accredited college or university)Master's Degree or equivalent preferred orPharmD or equivalent preferred orPhD or equivalent… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... (eg, Core Data Sheet generation/revision; clinical benefit-risk assessments for license renewals, responses to Health Authority)Participant and voting member in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and securing of pipeline- and portfolio-enhancing, business opportunities (through licensing , acquisition, co-promotion, and other structures). This role will, at ... other key stakeholders as indicated.- Meet with other pharmaceutical company licensing groups, participate in industry meetings.- Together with colleagues from… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …deviations from CCDS; review and approve CCDS/labeling agreements for licensing partners.Conduct Label Review Committee Meetings: Independently or through oversight ... of a team of GLLs, prepare labeling documents for review. Lead review processes to ensure appropriate review and governance by Daiichi Sankyo, and where applicable, partner companies for the development and approval of US, EU and global CCDS documents for… more
- Merck & Co. (Rahway, NJ)
- Job Description Director , Global Talent Operations The Director of Global Talent Operations is responsible for understanding the strategy from the Global Talent ... that strategy through resources supporting our company's talent management processes.- This director leads a team of 3-5 employees and is responsible for the… more
- Merck & Co. (Rahway, NJ)
- …cross-functional development teams to enable pipeline decisions. -The Executive Director , Biologics Analytical Research and Development (B-AR&D) is responsible for ... of Biologics programs (approximately 10-15 programs), and leading multiple Director lead Development teams, overall approximately 40-50 scientists. Strategic… more
- Merck & Co. (Rahway, NJ)
- …dedicated colleagues while developing and expanding your career. - The Senior Director (Senior Principal Scientist) has primary responsibility for the planning and ... particular focus on obesity and obesity-related metabolic disorders. - The Senior Director will manage the entire cycle of clinical development, including study… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Clinical Research Director (CRD) is the Clinical Operations lead in a country/cluster and is responsible-for execution of all Clinical Trials in ... relocationVISA Sponsorship:No Travel Requirements: 25%Flexible Work Arrangements:RemoteShift:Not IndicatedValid Driving License :NoHazardous Material(s):N/AJob Posting End Date:02/4/2025 *A job posting is… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJob Description Director -QP2-IO We are seeking an experienced talented scientist to join the - Quantitative Pharmacology and Pharmacometrics - - ... Immune/Oncology - (QP2-IO) - team in the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug… more
- Merck & Co. (Rahway, NJ)
- …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... compliance mindset and collaboration with various partners and stakeholders in development.The Director will report to the Executive Director of Biologics and… more
- Merck & Co. (Rahway, NJ)
- …at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate Director ... continuous basis in decision making and driving pipeline impact. The Associate Director will perform job duties independently with minimal supervision and/or lead… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director , Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) is accountable for the development and execution of ... TA dedicated global and regional directors and associate directors. The Executive Director , Value & Implementation (referred to as EDMA) engages with global… more
- Merck & Co. (Rahway, NJ)
- …and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and ... development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams of highly… more
- Merck & Co. (Rahway, NJ)
- …breakthrough science that radically changes the way we approach serious diseases. --The Director will report to an Associate Vice President in the Oncology Clinical ... Research Group. Under the guidance of a supervisor, the Director has primary responsibility for the planning and directing of clinical research activities involving… more
- Merck & Co. (Rahway, NJ)
- …Travel Requirements: 10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License :NoHazardous Material(s):n/aJob Posting End Date:01/31/2025 *A job ... posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R321791 more
- Merck & Co. (Rahway, NJ)
- …Travel Requirements: 10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License :NoHazardous Material(s):n/aJob Posting End Date:02/11/2025 *A job ... posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R328387 more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Biologics and Vaccines External Capabilities Director serves as the primary point of contact for all activities associated with outsourcing ... RegularRelocation:DomesticVISA Sponsorship:No Travel Requirements: 10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License :NoHazardous Material(s):n/aJob Posting End Date:02/21/2025 *A job posting is… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin us as an Executive Director of Tax Planning to lead our tax strategy for the US and navigate the ever-evolving global tax landscape. This ... Status: RegularRelocation:VISA Sponsorship: Travel Requirements: Flexible Work Arrangements:HybridShift:Valid Driving License :Hazardous Material(s):Job Posting End Date:02/8/2025 *A job posting is… more
