- 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
- Pfizer (New York, NY)
- The Associate Director , Clinical Diagnostics will support development of Diagnostics and Global Diagnostic Strategies across therapeutic areas. We are ... flow cytometry + An understanding of translational approaches as applied to clinical trial design and regulatory processes, proof-of-concept studies , and the… 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 ... where appropriate and escalate any complex problems to the Director , Clinical Study Startup. This... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and oversees… more
- Merck (Rahway, NJ)
- **Job Description** **Job Overview:** We are seeking a highly qualified and experienced Associate Director in Data Management to lead our data management team in ... supporting the pharm and vaccine veterinary clinical trials. The ideal candidate will be responsible for overseeing the development and maintenance of 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
- Takeda Pharmaceuticals (Trenton, NJ)
- … protocols, strategy slide decks, statistical analysis plans, briefing packages, clinical study reports, and regulatory labelling interactions. Ensure these ... innovative therapies across the oncology portfolio through: + Analysis of unmet clinical need and potential therapeutic preferences + Development of Clinical … 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 organization is accountable for managing the...ensures proper allocation of drug product as needed across studies within assigned program(s). + Responsible for identifying significant… more
- Mount Sinai Health System (New York, NY)
- …at Mount Sinai hospital. In collaboration with the MM Medical Director , the Associate Director , and the clinical trials investigators; this candidate is ... The Clinical Program Manager will report into Associate Director . **Qualifications** Education: + Bachelor's Degree...the protocol; and monitors test results, as appropriate Documents clinical study and therapy in patient's chart… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …across the Clinical Operations organization. + Provides oversight, and coaching to study teams to ensure diversity in clinical trial populations. + Applies ... the execution of diversity and inclusion strategy and tactics for global clinical trial programs. + Accountable for the co-creation and implementation of diversity… more
- Merck (Rahway, NJ)
- …the way we approach serious diseases. The Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of ... Director will manage the entire cycle of clinical development, including study design, placement, monitoring,...of Clinical Scientists in the execution of clinical studies . + Work closely with a… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …City, CA. This is NOT a remote position **RESPONSIBILITIES:** + In partnership with Clinical Program Manager or Associate Director , provides guidance and ... Plan, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans, Clinical Study Report + Coordinates data review to support… more
- Mount Sinai Health System (New York, NY)
- …all safety aspects of clinical research trial(s). Under guidance of the Associate Director of Research and Quality Outcomes, the CRA is responsible for ... Events (SAE) for safety reporting, CEC and DSMB of clinical studies to ensure compliance with regulations...is responsible for reconciliation of drug safety databases and clinical study databases for adverse event reporting… more
- Mount Sinai Health System (New York, NY)
- …Determines final testing parameters/procedures in conjunction with the ordering physician or clinical director and laboratory protocols. 3. Reviews the patient's ... science. Advancing medicine. Healing made personal. **Title: Sleep Technologist-Pediatrics Sleep Study Lab - MSH - 6PM-7:30AM** **_The Sleep Technologist works under… more
- Pfizer (New York, NY)
- **ROLE SUMMARY** + Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer ... and leadership to cross-functional activities, in collaboration with other statisticians, study managers, and programming colleagues, for assigned studies or… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …transformation templates for reuse for study level configuration tasks. The Associate Director Data Configuration Engineer (DCE) oversees a team that ... and empower you to shine? Join us as an Associate Director , Data Configuration Engineer in our...bold mission. **OBJECTIVES:** Key to Takeda's success is the Clinical Data Engineering team, provides strategic planning, integrating, execution,… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , RBQM - HOCT, ICN will mainly be responsible for ... 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 (New Brunswick, 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
- Taiho Oncology (Princeton, NJ)
- Associate Director , Outcomes Research & Real World Evidence Princeton, NJ, USA Req #389 Wednesday, September 4, 2024 Looking for a chance to make a meaningful ... Employee Value Proposition: Join our growing Medical Affair team in the role of Associate Director , Outcomes Research & RWE. Your expertise will play a pivotal… more
- Merck (Trenton, NJ)
- …questions from investigators and provides information regarding participation in company-sponsored clinical studies **Scientific Congress Support** + Engages in ... **Job Description** **Role Summary** + The Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD)… more