• Novo Nordisk Inc. (Plainsboro, NJ)
    Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety Surveillance. Essential Functions Innovation and ... or a life sciences/pharmacy nursing degree with 15+ years' experience in global safety surveillance and/or clinical /drug development Excellent verbal and written… more
    HireLifeScience (09/13/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …for operational improvements and seek agreement through consensus management.RelationshipsReports to an Associate Director / Director within the NNI ... Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent,… more
    HireLifeScience (09/12/24)
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  • Tris Pharma (Monmouth Junction, NJ)
    …have an immediate opening in our Monmouth Junction, NJ facility for an Associate Director , Alliance Management.Tris Pharma has a long track record of ... spanning many departments across all stages of the product lifecycle. The Associate Director , Alliance Management will be accountable for managing alliances… more
    HireLifeScience (08/26/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... plans from FIH to post registration. Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and lead study teams… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of relevant… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... value from inception through to implementation. Demonstrates ability to handle global projects through established interactions with Japan and Europe as required.… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for ... and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess...study teams regarding regulatory requirements and ICH guidance for clinical documents.Participate in initiatives within the Global more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …as other research areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of ... Global Medical Affairs' externally sponsored clinical research (ESR) initiatives, ensuring strict adherence to Good Clinical Practices (GCPs), relevant… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …business functions of Daiichi Sankyo (DS) in the US, EU, Japan, and other global sites. These business functions include: Clinical Operations, Clinical ... medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... team and serves as ad hoc member to the Global Project Team for late stage projects. This position...technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing… more
    HireLifeScience (09/13/24)
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  • Legend Biotech USA, Inc. (Piscataway, NJ)
    …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development ... Company InformationLegend Biotech is a global biotechnology company dedicated to treating, and one...cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo… more
    HireLifeScience (07/26/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for medium complexity… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …robust publication plans for the Therapeutic Area and respective products. Mentor Associate Director Publication leads on publication planning and execution ... other research areas centered around rare diseases and immune disorders. Summary Director , Global Medical Affairs Oncology Publications works with Cross… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Manager role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This ... share with study team, Operations Program Lead, and Sr. Director for the compound, on regular basis and ensure...The Study Team Leader will work closely with the Global Clinical Lead to ensure alignment. CRO,… more
    HireLifeScience (09/13/24)
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  • Associate Director , Clinical

    AbbVie (Branchburg, NJ)
    …Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Clinical Development will have global or regional ... Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director ,...accountable for the development, implementation, and delivery of the global clinical development strategy for a given… more
    AbbVie (09/12/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical more
    Regeneron Pharmaceuticals (07/04/24)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …opportunity employer including veterans and people with disabilities. **Summary** The Associate Director will be responsible for developing and implementing ... plans from FIH to post registration. Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and lead study teams… more
    Daiichi Sankyo Inc. (08/22/24)
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