- Daiichi Sankyo, Inc. (Bernards, NJ)
- …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 Standard… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and presentation skills.Responsibilities- Demonstrates strong knowledge of the industry, vendor base, and regulatory issues for respective categories. Leads the ... of sourcing strategy for respective categories. Builds and maintains a good vendor base. Manages vendor relationships. Implement sourcing and value development… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …US, EU, Japan, and other global sites. These business functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory ... Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies ... fulfill regulatory requirements and deliver the pre-specified product profile.CRO / Vendor Oversight: Review CRO/ vendor proposal and budget. Establishes… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for medium complexity ... fulfill regulatory requirements and deliver the pre-specified product profile.CRO / Vendor Oversight: Review CRO/ vendor proposal and budget. Establishes… more
- 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 ... research areas centered around rare diseases and immune disorders. Summary Director , Global Medical Affairs Oncology Publications works with Cross Functional Team… more
- 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...Clinical Lead to ensure alignment. CRO, 3rd Party Vendor Management and Oversight:Responsible for the oversight, performance, and… more
- Eisai, Inc (Nutley, NJ)
- …models.Generating advanced insights and predictive capability from statistical models. Clinical development and product life-cycle management. Vendor ... this is your profile, we want to hear from you. Director , Global RWE & Data Science sought by a...programs in support of global market access initiatives. Lead clinical meaningfulness initiatives that address issues such as payer… more
- Eisai, Inc (Louisville, KY)
- …with internal cross functional partners including but not limited to Associate Director Regional Marketing, Oncology Field Reimbursement Managers, and ... utilization of promoted Oncology therapeutic products for specific indications; deliver clinical , efficacy, and safety messaging to target physicians in a compliant… more
- Eisai, Inc (San Diego, CA)
- …with internal cross functional partners including but not limited to Associate Director Regional Marketing, Oncology Field Reimbursement Managers, and ... utilization of promoted Oncology therapeutic products for specific indications; deliver clinical , efficacy, and safety messaging to target physicians in a compliant… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Outsourcing & Vendor Management Pleasanton, CA, USA * Princeton, NJ, USA Req #385 Friday, August 16, 2024 Looking for a chance to make a ... Value Proposition: Join our dynamic and expanding mid-size company in the role of Associate Director , Outsourcing and Vendor Management. Your expertise will… more
- Lilly (Indianapolis, IN)
- …of ICH and quality guidelines needed for successful delivery of the portfolio and clinical trials, the Associate Director / Director Relationship Manager ... for people around the world. The purpose of the Associate Director / Director Relationship Manager role...partner in the issue escalation and relationship management processes, vendor , and clinical research unit assessments as… more
- Amgen (Washington, DC)
- …10 million patients worldwide. It's time for a career you can be proud of. ** Associate Director Global Clinical Program Management, Obesity - US, Remote** ... Line Management of Global Trial Managers (GTM)s + Supports Clinical Program Operations (CPO) Director /Snr Director...years life sciences or medically related experience working on clinical trials OR Associate 's degree and 12… more
- Kelly Services (Alameda, CA)
- ** Associate Clinical Supplies Director **...+ Are willing to travel up to 20% to vendor sites, team meetings, and/or other offices. **What happens ... in your backyard. Kelly(R) Science & Clinical is looking for an ** Associate Clinical Supplies Director ** to work at an **innovative biotech company** in… more
- Lilly (Indianapolis, IN)
- …policy and guidance to speed the delivery of medicines to patients globally. The Associate Director - Clinical Results Reporting Systems role requires broad ... to make life better for people around the world. Clinical Trial Foundations as part of Clinical ...Tech@Lilly, and other components of the R&D organization, the Associate Director - Results Reporting Systems is… more
- CSL Behring (King Of Prussia, PA)
- …or Amsterdam office. It is a Hybrid role. You will report to the Director Clinical Portfolio Execution. You will develop the operational strategy for a ... take on additional responsibilities as defined by the (Sr) Director Clinical Portfolio Execution. This role may...**Other degrees and certifications considered if determined by related clinical research experience (eg, diploma or associate … more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Associate Director of Drug Metabolism and Pharmacokinetics is responsible for outsourcing, oversight and monitoring of Drug Metabolism and ... Monitors DMPK cost and resource projections and support accounting practices for clinical study budget management. + Contributes to vendor qualification and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …specializes in process improvements, procedural documents, and quality and inspection readiness for Clinical Operations. The Associate Director , will be a ... collaborative approach to proactive compliance activities. + Key stakeholders include clinical systems, TMF, RBQM, Vendor quality/oversight, thus direct… more
- BeiGene (San Mateo, CA)
- The Associate Director (AD) Clinical ...to study specifications and that sites are responsive to vendor to meet the deliverable **Budget** + Liaises with ... vendors and external budget to ensure the timely and cost-effective implementation of clinical trials. Provides guidance and direction to assigned staff, as well as,… more
- Bristol Myers Squibb (Princeton, NJ)
- …enable Global Development Operations (GDO) function, specifically focusing on Veeva Clinical Vault (Veeva CTMS, Veeva eTMF). This role owns end-to-end responsibility ... behind them to ensure the digital capabilities are cost efficient. + Influence vendor roadmaps to align with BMS strategy. Requirements: + Must have 10+ years… more
