- Bristol Myers Squibb (Berkeley Heights, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Clinical Data Standards is a leadership ... Director , Head Standards Management & Steward within Clinical & Safety Data Insights and Analytics....Insights and Analytics. **Position Responsibilities** + Providing leadership of clinical data standards activities across multiple … more
- 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix ... join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads...and designs mitigation strategies + Promotes consistent first line medical/ clinical data review techniques and conventions across… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Clinical Sciences contributes to the development, evaluation, planning and execution of hematology clinical studies and ensures ... on clinical studies and programs. As an Associate Director , a typical day may include...and designs mitigation strategies + Promotes consistent first line medical/ clinical data review techniques and conventions across… more
- AbbVie (Branchburg, NJ)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Clinical Development will have global or ... Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director ,... content, including, but not limited to protocols, IBs/IDFUs, clinical data reviews, CSRs, regulatory submissions, and… more
- Bristol Myers Squibb (Summit, NJ)
- …+ Advanced Degree in related field (MS, Ph.D. or PharmD) + For Associate Director level with Ph.D. approximately 5+ years experience with demonstrated ... and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. Composed of pharmacologists, pharmacometricians, data … more
- Touro University (New York, NY)
- …effective July 1, 2023 (pending budget approval). The Program Director and Associate Professor the master's program in Clinical Mental Health Counseling is ... Overview MS in Clinical Mental Health Counseling program at Touro University...Sciences invites applications for a full-time position as Program Director and Associate (or higher) Professor. Position… more
- System One (Basking Ridge, NJ)
- Associate Director , Clinical Safety...Health Authority inquiries on safety issues and prepares safety data for safety review boards. + Present safety ... plus + international MD is okay + 1-3 years of Pharmacovigilance (PV)/ clinical safety experience in pharmaceutical drugs either from relevant work experience within… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …the treatment of bipolar depression in adults as monotherapy and as adjunctive therapy. ** Associate Director / Director , Data Management** will oversee and ... Director : Minimum of 7 years of experience in Data Management in pharmaceutical clinical trials (preferably...veteran status, disability or any other legally protected status. Associate Director , Data Management: Base… 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
- Merck (Rahway, NJ)
- **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories (Research and Development Division) portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling, packaging… more
- Mount Sinai Health System (New York, NY)
- …team, a research clinical data warehouse team and a research data services team. The Associate Director , High Performance Computational and ... along with a focus on world-class customer service. The Associate Director is a productive partner for...file system,40+ petabyte archival storage system, and a research clinical data warehouse with a high availability… more
- Bristol Myers Squibb (Madison, NJ)
- …and centralized monitoring for trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a leadership role ... position. **Position Responsibilities include:** + Providing leadership of external clinical data acquisition and integration activities across multiple… more
- Bristol Myers Squibb (Madison, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , US Medical, Multiple Myeloma will report to the ... MM asset lead and the MM Medical Lead. The Associate Director will provide key contributions for... clinical trials in hematology/oncology. + Proficiency in clinical data review and interpretation. + Excellent… more
- Bristol Myers Squibb (Madison, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , WW Cell Therapy Medical, Operations and Product Science ... will report to the Executive Director CT Medical Franchise. He/she will expected to attend...as therapeutic area expert in Cell Therapy and provide clinical /scientific leadership and support for approved CAR T products… more
- Bristol Myers Squibb (Madison, NJ)
- …by leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... for managing the end-to-end process for IC for BMS-sponsored clinical trials. This includes a centralized triage function for... Director of Informed Consent Management. The AD will be… more
- AbbVie (Florham Park, NJ)
- …Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business ... and responses, and other program documents. *May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical Scientists working… more
- J&J Family of Companies (Raritan, NJ)
- Associate Director , Global Real World Evidence (RWE) Oncology (Solid Tumor) - 2406216357W **Description** Johnson & Johnson Innovative Medicine is recruiting an ... Associate Director , Global Real World Evidence (RWE),...Global Market Access, Global Marketing, Global Epidemiology, J&J Technology Data Sciences, Janssen R&D Data Science, reginal… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** ** Associate Director , Biostatistics** **Position Overview:** Biostatisticians at Gilead ... colleagues to ensure appropriate design, statistical analysis and reporting of Gilead clinical data in efficiently achieving regulatory, scientific and business… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Job Summary:** The Associate Director of Regulatory Writing is a key role responsible for ... producing scientifically accurate, high-quality clinical regulatory documents while adhering to regulatory guidelines. This...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more