- 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
- Gilead Sciences, Inc. (Parsippany, NJ)
- …their aspirations. Join Gilead and help create possible, together. **Job Description** ** Associate Director , Clinical Pharmacology - Virology** **_*This is ... and study sites to implement and monitor clinical pharmacology studies . Addresses clinical ...regulations, ICH guidelines, and GCP governing the conduct of clinical studies . Has significant knowledge of pharmaceutical… 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
- Merck (Rahway, NJ)
- …operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...ensures proper allocation of drug product as needed across studies within assigned program(s). + Responsible for identifying significant… more
- Bristol Myers Squibb (Madison, 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
- AbbVie (Florham Park, NJ)
- … development projects. A visible and collaborative role, the Associate Director / Director works in partnership with clinical and regulatory experts ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director / Director , Statistics (Dermatology) provides scientific… 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
- Mitsubishi Chemical Group (Jersey City, NJ)
- …hard copy and/or electronic solutions for data acquisition in MTPA clinical development studies . The Associate Director functions in a department with a ... oversight of data management for clinical development studies within all MTPA therapeutic areas. The Associate... studies within all MTPA therapeutic areas. The Associate Director works with departmental and cross-functional… more
- Merck (Rahway, NJ)
- **Job Description** **Title: Associate Principal Scientist/ Associate Director , Outcomes Research** **Role Summary** + Under the guidance of a senior leader, ... an Associate Principal Scientist/ Associate Director , has...In collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires,… more
- Bristol Myers Squibb (Summit, 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 (Madison, 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
- Bristol Myers Squibb (Summit, 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 (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 ... trial design, analysis planning, study results presentation and interpretation, clinical study report authoring, regulatory submissions and publications. +… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …on real-world evidence, and creating hope for all facing illness. The Associate Director , Biostatistics is responsible for providing statistical support to ... Contributes to the design, conduct, analysis, and interpretation of clinical studies and research projects. + Performs...Provides sample size estimates and power calculations for complex study designs. + Reviews protocols and case report forms… more
- Merck (Rahway, 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
- Merck (Rahway, NJ)
- …programs. + In collaboration with internal teams and external partners, design studies , author study protocols, develop measurement questionnaires, case report ... to reimbursement and market access, and provide input into clinical , regulatory, payer/access, marketing and evidence generation strategies and...forms, data analysis plans, final study reports, scientific presentations, and publications.… more
- Merck (Rahway, NJ)
- …and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and execution of design ... and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …global Clinical Drug Supply & Logistics category. We are looking for an Associate Director Global Procurement to manage categories with a high degree of ... Regeneron. + Success running cross-functional teams to get results in Clinical Trial categories or related categories through effective sourcing, negotiations,… more
- IQVIA (Parsippany, NJ)
- **Job Summary:** The Associate Legal Operations Director will be responsible for supporting key strategic, organizational, and financial initiatives within ... as needed. **Qualifications:** + Bachelor's degree in Business Administration, Finance, Legal Studies , or a related field. + Minimum of 5 years of experience… more