- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix ... clinical studies and programs. As an Associate Director a typical day may include...in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study progress. + Manages all aspects of Quality ... quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable...with senior level management, external vendors, collaboration partners and clinical study personnel for clinical … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Develops biomarker strategy in collaboration with Translational Medicine/Clin Pharm; May act as Clinical study leader (CSL) + Study Planning and Execution: ... Provides medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams. **Responsibilities** + Study Strategy:… more
- Bristol Myers Squibb (Princeton, NJ)
- …and success of the BMS R&D pipeline. This role reports to the Director , Clinical Data Management or Associate Director , Clinical Data Management ... is responsible for: **Project Management and Leadership** + Provides clinical data management leadership within the study ...Provides clinical data management leadership within the study team to align on and drive data collection… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic... trial performance and quality metrics and share with study team, Operations Program Lead, and Sr. Director… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . Position Summary The Associate Director , RBQM - HOCT, ICN will mainly be responsible ... and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and...compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to ensure… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Oncology & Hematology, Medical Evidence Generation will: + ... concepts to full proposals and aid in site assessment/recommendation, facilitation of study design, presentation to governance in partnership with disease area leads… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Product Development Princeton, NJ, USA Req #448 Thursday, March 6, 2025 Looking for a chance to make a meaningful difference in the oncology ... responsible not only for product development but also support clinical studies , commercialization and life-cycle management. You...is the role for you. Position Summary: + The Associate Director , Product Development will be responsible… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be ... protocols using data and information from discovery phase, non- clinical and clinical studies +...that GxP follow-up CAPA activities are completed + Oversee study centers, countries, investigators and connect with PV, Medical… more
- Bristol Myers Squibb (Princeton, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... trial design, analysis planning, study results presentation and interpretation, clinical study report authoring, regulatory submissions and publications. +… more
- Sumitomo Pharma (Trenton, NJ)
- …. **Job Overview** The ** Associate Director , Medical ... launch strategy and guide the tactical implementation of Medical Affairs plans. The Associate Director will also collaborate with company outreach and patient… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Medical Surveillance Princeton, NJ, USA Req #435 Tuesday, February 11, 2025 Looking for a chance to make a meaningful difference in the ... and written communication, planning, organization, with knowledge of the investigational clinical study and post-marketing settings. + Working knowledge of… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Sciences Princeton, NJ, USA Req #444 Thursday, February 27, 2025 Looking for a chance to make a meaningful difference in the oncology ... Value Proposition: Embark on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the forefront of pharmacovigilance… more
- Merck (Trenton, NJ)
- …**Quantitative Pharmacology and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- BeiGene (Pennington, NJ)
- **_General Description:_** Establish a stability program in Quality Control for clinical and commercial phase biologics products in accordance to FDA/EU regulations, ... and BeiGene processes and procedures. Oversee and manage stability studies to deliver scientifically sound GMP test data in...+ Establish and manage the QC stability program for clinical and commercial phase biologics products. + Ensure timely… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director of Statistical Methodology and Innovation works closely ... rigor and innovation, operational feasibility, and resource efficiency across the BMS portfolio. Associate Director of Stat Methodology role will be involved in… more
- System One (Raritan, NJ)
- Title: Manager, Associate Director , Medical Writing Location: Remote Salary: 150-165K depending on experience Type: Embedded Start Date: ASAP Leading ... Pharmaceutical Company located in NJ is hiring a Associate Director , Medical Writing w/ 5+ years...of publication plans and strategy at the individual dataset, study , and/or compound level. + Skillfully manage projects through… more
- J&J Family of Companies (Raritan, NJ)
- …approved by the Company. **We are searching** **for the best talent for** ** Associate Director , North America Regulatory Leader** **to** **be in Raritan, NJ.** ... + Provide strategic regulatory input to key development documents, including clinical protocols, statistical analysis plan, clinical and nonclinical reports… more
- Novo Nordisk (Plainsboro, NJ)
- …for a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will provide strategic ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion. Essential Functions… more
- Sanofi Group (Bridgewater, NJ)
- …Join our **Biostatistics Immunology & Inflammation as Statistical Project Leader ( Associate Director )** and you'll provide statistical leadership and guidance ... responsibilities:** + Expert level of statistical and scientific contribution to clinical development plans, studies and submissions activities (when… more