- Lilly (Branchburg, NJ)
- …for this position is $111,000 - $162,800 **Position Description:** The Clinical Trial (CT) Supply Management Associate Director will provide operational ... to improve performance and speed drug development. **Responsibilities:** + Deliver improved clinical trial supply chain performance, assess and mitigate risk,… more
- Bristol Myers Squibb (Madison, NJ)
- …and implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative relationships and ... development and implementation of technical solutions for integrating, analyzing and reporting clinical data. Associate Director drives the development… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... + Study Planning and Execution: Provides input on major milestones of trial , clinical trial plan and contingency planning; Analyzes and updates management… more
- Pfizer (New York, NY)
- The Associate Director , Clinical Diagnostics...with Asset Teams to manage the timely testing of clinical trial samples and the analysis and ... flow cytometry + An understanding of translational approaches as applied to clinical trial design and regulatory processes, proof-of-concept studies, and the… more
- Mount Sinai Health System (New York, NY)
- …safety aspects of clinical research trial (s). Under guidance of the Associate Director of Research and Quality Outcomes, the CRA is responsible for ... clinical studies as a clinical trial assistant or clinical research associate...for adjudication by the CEC. + Participates with the Director of Research and Quality Outcomes in the preparation,… more
- Penn Medicine (Plainsboro, NJ)
- …to day operations of clinical research proposals for their team. The Associate Director will work with Investigators and data informatics teams/programs to ... living your life's work? We are hiring for an Associate Director Oncology Research Operations to join...Specialist, Billing Compliance staff, and Finance office to develop clinical trial budgets. Communicating any specialized study… more
- Bristol Myers Squibb (Madison, NJ)
- …This includes a centralized triage function for informed consent negotiations with global clinical trial sites, IRBs/ECs, and health authorities, as well as ... internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role...Simplification. + Knowledge of IT systems used to support clinical trial processes and the authoring of… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Purpose** The Associate Director , Biostatistics is a core member of cross-functional ... leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning,… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning,… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Biostatistics Princeton, NJ, USA Req #421 Monday, December 23, 2024 Looking for a chance to make a meaningful difference in the oncology ... Summary: + This position will have direct responsibility including clinical trial design and execution, analysis and...data, and authoring/review of scientific and regulatory documents. The Associate Director of Biostatistics will have CRO… more
- Merck (New York, NY)
- **Job Description** The Regional Medical Scientific Associate Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in ... SL inquiries on issues outside of Regional Medical Scientific Director scope (eg, grants) to appropriate company resources consistent...to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study… more
- Merck (Rahway, NJ)
- …component of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Vendor Management, is responsible for assessing, onboarding, and overseeing the health and performance of vendors involved in clinical ... reviews and updates of business continuity plans. + Ensure minimal disruption in clinical trial operations through effective continuity planning. + Contribute to… more
- AbbVie (Florham Park, NJ)
- …substantial understanding of relevant therapeutic area required. + Knowledge of clinical trial methodology, regulatory requirements governing clinical ... level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational… more
- Pfizer (New York, NY)
- …communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results **,** ... biostatistics, or related field. + A minimum of 4 years' experience in the clinical trial setting (preferably in oncology of Pharma). + Relevant clinical … more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** ** Associate Director , Biostatistics** **Position Overview:** Biostatisticians at Gilead ... data in efficiently achieving regulatory, scientific and business objectives. The Associate Director will be primarily responsible for the business,… more
- IQVIA (New York, NY)
- ** Associate Director , IQVIA Participant Payments (ADIPP)** The Associate Director , IQVIA Participant Payments (ADIPP) is responsible for directing a ... **_Experience_** + 5-7 Years of prior experience with global participant payments, clinical trial payments, and/or other payment processing + Requires practical… more
- Bristol Myers Squibb (Madison, NJ)
- …synopses and protocols. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol ... coordination with clinical plans and marketing objectives. + Experience with clinical trial assays (CTA) in drug clinical trials in communicating between… more
- Novo Nordisk (Plainsboro, NJ)
- …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions + Serve as a… more
- Bristol Myers Squibb (Madison, NJ)
- …across a matrix. * Experience with drug development, commercialization, and healthcare, clinical trial management a plus. **\#LI-Hybrid** If you come across ... Cell Therapy (CT) Organization. **Details** This role reports directly into the Senior Director of Strategy and Operations and will be a strategic and operational… more