- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data ... (SOPs) within assigned program(s). The PDML is a member of the Clinical Data Management extended leadership team, and as such interacts with senior level… more
- Bristol Myers Squibb (Madison, NJ)
- …design, development and implementation of technical solutions for integrating, analyzing and reporting clinical data . Associate Director drives the ... development and implementation of innovative strategies and technologies for clinical trial programming. Associate Director ...medical terminology used in the analysis and submission of clinical data + Broad expertise in statistical… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and that quality of data is suitable for regulatory submission. The Associate Director will have routine interaction with key internal and external ... master file is complete and accurate for assigned stud(ies). + If assigned, Associate Director , Clinical Operations may act as the Study Team Leader for… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …around rare diseases and immune disorders. **Summary** This position works with the Director , Clinical Study Startup to establish the strategy driving global ... Plans and may perform final review. This position provides input on electronic data capture (EDC) Safety report outputs, reviews clinical study and… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** Job Description ** Associate Director , Clinical Pharmacology - Oncology** **_*This is ... the respective cross-functional study team. + With input from others, designs clinical pharmacology study protocols, study data analysis, modeling and simulation… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment ... size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member...+ Study Strategy: Provides the strategic direction to Biostats Data Mgmt & Data Ops for EDC,… more
- AbbVie (Florham Park, NJ)
- …level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational ... professional and provider interactions (HCP's, Patients and Payers); generation of clinical and scientific data (enhancing therapeutic benefit and value);… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** The HEOR Associate Director - BU based is accountable for ensuring execution of HEOR projects for priority pipeline programs, ... us. Job Description: Specimen Management Business Unit-JG5 **Position Summary** The HEOR Associate Director for the Specimen Management business is accountable… more
- Bristol Myers Squibb (Madison, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Media Category Lead is responsible for development of a ... of contact for Commercialization-related procurement needs. This will require the Associate Director Procurement Media to have strong coordination, collaboration… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Associate Director , Market Access, Payer Marketing Date: Dec 19, 2024 Location: Parsippany, United States, New Jersey, 07005 Company: Teva Pharmaceuticals Job ... people to make a difference with. **The opportunity** The Associate Director of US Payer Marketing works...and pull through program effectiveness through various IT and data resources. + Attend various market access and relevant… more
- Bristol Myers Squibb (Madison, NJ)
- …careers.bms.com/working-with-us . **Summary:** Join our People Science team as our next Associate Director , Employee Listening Lead, where you'll play a crucial ... workforce strategy through the power of employee feedback and data . We are looking for a dynamic leader who...unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation,… more
- IQVIA (Parsippany, NJ)
- ** Associate Director , IQVIA Participant Payments (ADIPP)** The Associate Director , IQVIA Participant Payments (ADIPP) is responsible for directing a ... + 5-7 Years of prior experience with global participant payments, clinical trial payments, and/or other payment processing + Requires practical knowledge… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …and unique opportunity for a medical writer to join our dynamic team at the Associate Director level. You will author a wide range of regulatory documents ... variety of documents of all types and complexities, such as clinical study reports (CSRs) (all phases), investigator's brochures, CTD summaries/overviews, PIPs/PIP… more
- AbbVie (Florham Park, NJ)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: The Associate Director in CMC Statistics is responsible for providing statistical ... strategy meetings. Contribute to strategic planning to ensure statistically optimized non- clinical development plans and assist in the creation of strategic… more
- Bristol Myers Squibb (Madison, NJ)
- …Cell Therapy (CT) Organization. **Details** This role reports directly into the Senior Director of Strategy and Operations and will be a strategic and operational ... across a matrix. * Experience with drug development, commercialization, and healthcare, clinical trial management a plus. **\#LI-Hybrid** If you come across a role… more
- Lilly (Morristown, NJ)
- …The anticipated wage for this position is $145,500 - $213,400 Scientific and Clinical Experts (SEs/CEs) are individuals who are noted for their expertise in a ... By facilitating scientific exchange between industry and the scientific and clinical communities, MSLs shape the future of healthcare by providing the… more
- Bristol Myers Squibb (Madison, NJ)
- …and protocols. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments in ... team development. + Experience with developing regulatory strategies in coordination with clinical plans and marketing objectives. + Experience with clinical … more
- AbbVie (Florham Park, NJ)
- …leads those efforts. Anticipates and critically evaluates Statistical, PK/PD, Clinical Pharmacology, or regulatory advances, strengths, weaknesses, opportunities and ... for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: + Executes strategy,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …functions include but are not limited to 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 Research, Research,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …+ Has a comprehensive understanding of the functional roles within Pharmacovigilance and Clinical Trials + Ability to extract configurable data fields from a ... activities of Daiichi Sankyo Pharmacovigilance Safety systems, and fulfillment of data change requests. **Responsibilities** **Change Requests for PV Systems** +… more