- 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 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)
- …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)
- …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
- 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
- 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
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , TA (Therapeutic Area) Analysis Standards Leader is ... across the TA, aligning cross-functionally and driving end to end standards. Associate Director , TA Analysis Standards Leader, independently leads improvement… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Regulatory Affairs Operations Pleasanton, CA, USA * Princeton, NJ, USA Req #386 Tuesday, August 20, 2024 Looking for a chance to make a ... Join our dynamic and expanding mid-size oncology company in the role of Associate Director , Regulatory Affairs Operations where you will utilize your knowledge… more
- Bristol Myers Squibb (Princeton, NJ)
- …managing outsourcing within a specific therapeutic area. The role involves overseeing clinical trial vendor partnerships across multiple service categories and ... the main point of contact for outsourcing at the trial level, facilitating vendor selection, managing Statements of Work (SOWs), and overseeing vendor … more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Programming in Cambridge, MA, where you will oversee and ... & Quantitative Sciences team, you will report to the Director , Programming. Takeda SQS is looking to add individuals...**contribute:** + Oversee and direct the work of the Clinical trial disclosure programming team (within the Programming Center… more
- J&J Family of Companies (Raritan, NJ)
- Associate Director , Solid Tumors Global Commercial Insights & Analytics - 2406208396W **Description** Johnson & Johnson Innovative Medicine is recruiting for an ... Associate Director , Solid Tumors Global Commercial Insights...as well as key competitors' strategies and tactics for clinical development and commercialization and translating insights into implications… more
- Daiichi Sankyo Inc. (Basking Ridge, 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...studies involving multiple currencies and complex financial tracking. + Vendor and Site Management: Direct and enhance interactions with… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... and executes a labeling implementation plan to incorporate new scientific, safety and clinical data, as well as Health Authority responses / feedback into CCDS, USPI… more
- System One (Basking Ridge, NJ)
- Job Title: Associate Director , Biostatistics Client: Global Pharmaceutical Company Location: Remote, US Based only - must reside in EST or CST time zones Type: ... Must Haves: Oncology lead experience. PhD 5+ years Oncology clinical trial experience OR Master in Biostatistics - 8+...requirements and deliver the pre-specified product profile. CRO / Vendor Oversight: Review CRO/ vendor proposal and budget.… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …presentation skills. **Responsibilities** - Demonstrates strong knowledge of the industry, vendor base, and regulatory issues for respective categories. Leads the ... strategy for respective categories. Builds and maintains a good vendor base. Manages vendor relationships. Implement sourcing...or More Years Outsourcing, health sciences or related field ( clinical trials) required - 7 or More Years Deep… more
- Daiichi Sankyo Inc. (Basking Ridge, 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. (Basking Ridge, NJ)
- …Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for medium complexity ... and deliver the pre-specified product profile. + CRO / Vendor Oversight: Review CRO/ vendor proposal and budget....profile. + CRO / Vendor Oversight: Review CRO/ vendor proposal and budget. Establishes procedures through regular interaction,… more
