- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …Administration and under limited direction, the Contracts Manager - Federal Contracts and Compliance, will oversee end-to-end contract management for the ... participating in and monitoring LBRI's ongoing performance on federal contracts to ensure adherence to contract terms...the daily operations of the LBRI Office of Research Contracts . Will work closely with the Director … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …A Bachelor 's Degree in Business or equivalent experience. MBA or another advanced degree preferred. 15+ years of progressively relevant business experience in areas ... About the Department Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions that drive patient access to innovative products. We strive to deliver the best possible… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(for both US and Global), from Request for Proposal (RFP) to final contract . This position has direct oversight and accountability of Category leads to drive ... strategic sourcing responsibilities. Leads complex supplier negotiations and commercial contracts for quality and value creation. Enhances the procurement capability… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director , Global Payroll Strategy and US Payroll Leader has responsibility for the delivery of HR payroll for approximately 26,000 US employees as ... relationships and on-going delivery strategy.-This positionreports to the Executive Director , HR Regional Services.- --Position location: Rahway, New Jersey or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …For studies in which Medical Monitoring activities are conducted by the Contract ResearchOrganization (CRO) Medical Monitor (MM):- Provides oversight to the CRO MM ... for clinical data review activities- May support addressing eligibility and medical questions from sites/ IRBs- May provide medical guidance for coding of AEs, medical history, and medications when needed- Clinical Development Expertise Strategy- In… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description: Associate Director , Site Services Procurement (NORAM) This Procurement Associate Director role will be a member of the ... Management with key suppliers to maximize supplier performance, ensure contract compliance and delivery of contractual commitments, and optimize supplier… more
- Daiichi Sankyo, Inc. (Boston, MA)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director Field Reimbursement (ADFR) is a critical front-line member of the DSI ... DSI oncology field staff to ensure aligned customer approach. Proactively communicate contract and formulary status relevant to each hospital and clinic account to… more
- Daiichi Sankyo, Inc. (Seattle, WA)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director , Field Reimbursement (ADFR) is a critical front-line member of the DSI ... DSI oncology field staff to ensure aligned customer approach. Proactively communicate contract and formulary status relevant to each hospital and clinic account to… 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 ... studies in which Medical Monitoring activities are conducted by the Contract Research Organization (CRO) Medical Monitor (MM):Provides oversight to the CRO… more
- Tris Pharma (Monmouth Junction, NJ)
- …immediate opening in our Monmouth Junction, NJ facility for an Associate Director , Alliance Management.Tris Pharma has a long track record of successful alliances, ... many departments across all stages of the product lifecycle. The Associate Director , Alliance Management will be accountable for managing alliances of high… more
- Tris Pharma (Monmouth Junction, NJ)
- …Junction, New Jersey, Tris has an immediate opening for a full-time permanent Director /Senior Director , Clinical Quality Assurance. This is a hybrid position. ... with experience.SUMMARY:Reporting to the Chief Quality Officer the Senior Director of Clinical Quality Assurance provides strategic leadership and direction… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …multiple biological developmental projects with supervision, including working with contract manufacturing organizations CMO. This position serves as the Regulatory ... multiple biological developmental projects with supervision, including working with contract manufacturing organizations CMO. This position develops strategy, prepares… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …growth and provide development opportunity for statistical programmers. Manages contract statistical programming staff to ensure proper resource allocation for ... negotiations and provides oversight of budget, resources, and timelines for contract research organizations (CROs) for multiple projects and ensures timely delivery… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Health Authorities globally with some supervision. This position also guides contract research organization (CRO) programmers and statisticians in preparing analysis ... files and performing statistical analyses. Additionally, this position interacts with study teams, as well as statisticians and programmers at CROs. This position works under some supervision to solve complex study problems. Responsibilities Protocol… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Supports PhRMA Board Member, as needed.- Manage state government consultants, and contract lobbyists as required, to ensure their work advances Daiichi Sankyo's ... priorities and brings sustained value to the organization.- Support Government Affairs Public Policy team in other areas, as needed, to move Daiichi Sankyo goals forward. Qualifications: Successful candidates will be able to meet the qualifications below with… more
- Merck & Co. (Rahway, NJ)
- …of employment related litigation.Represent the Company in labor arbitrations, contract negotiations and labor proceedings.Prepare severance agreements.Assist in the ... development, review and revision of employment policies.Support our Company's HR teams and compliance functions in audits and internal investigations.Provide training to HR and line management teams on employment related issues.Work with and potentially train… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …globally. Provide QA oversight of GLP/GCLP activities of Daiichi Sankyo, contract research organization/ vendors ensuring that outsourced obligations are in ... compliant and prepared for regulatory submissions and / or inspections Ensures that appropriate systems, processes are in place to enhance GLP/GCLP activities being executed at DS cross-functional teams (ie , Research, Translational Oncology, GDO etc.,).Serve… more
- Insmed Incorporated (San Diego, CA)
- …Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , Quality Assurance - Analytical,GMP has responsibility for the QA ... procedures for intended useApprove and monitor analyses carried out under contract through private labsLead the activities associated with monitoring the maintenance… more
- Eisai, Inc (Nutley, NJ)
- …provisioning.Negotiate and administer vendor, outsourcer, and consultant contracts and service agreements.Develop requests for proposal.Operational Management ... 25% Direct the deployment, monitoring, maintenance, development, upgrade, and support of business systems, including applications, integrations and infrastructure upgrades in conjunction with business process owners and infrastructure teams.Oversee provision… more
- Eisai, Inc (Raleigh, NC)
- …several of which must be in a people management position.Prior contract manufacturing project management experience is highly preferred. Prior experience with ... manufacturing from pre-IND through phase 3 or commercial production is highly desired.Significant knowledge of biologics manufacturing and analytical methodology as well as ICH, cGMP, EMEA and JP guidelines as they pertain to the manufacturing of monoclonal… more
