- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …as well as other research areas centered around rare diseases and immune disorders. Summary The Director , Clinical Safety , will be a product safety lead ... specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-marketing… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …centered around rare diseases and immune disorders. SummaryThis position supports safety monitoring and risk management activities, provides insights on current ... clinical practice and guidelines, reviews and provides written assessments...position supports a senior physician in evaluating and mitigating safety signals as they arise. Additionally, this position works… more
- Eisai, Inc (Nutley, NJ)
- …the therapeutic area and 3 years in an in-house Medical Affairs role; MD preferredClinical research experience, including conducting clinical trials in the Phase ... If this is your profile, we want to hear from you.The Medical Director , US Medical Affairs provides medical leadership for medical affairs strategy, planning and… more
- Eisai, Inc (Nutley, NJ)
- …your profile, we want to hear from you. Job Summary The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive ... tactics for assigned therapeutic area. Under the direction of the Senior Medical Director , this role will be responsible for working with key stakeholders to develop… more
- Merck & Co. (Rahway, NJ)
- …Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be responsible for:-Evaluating pre- clinical and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization ... dedicated to the effective strategy, design, execution, and interpretation of Oncology clinical trials. Position Summary / Objective Serves as a primary source of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Represents Clinical Development in Project Teams, possibly as Global Clinical Lead.Responsibilities:Medical Monitoring Planning ( MD Only): For large Phase 2 ... and geographic scope. Such trials could be pivotal for submission; Prepares clinical section of regulatory documents; Oversees management and performance of CRO;… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …known for accelerated development and approval with smaller numbers of subjects exposed, Clinical Safety and Pharmacovigilance (CSPV) must be embedded in R&D as ... possible. This led us to create the Translational Patient Safety Senior Director position, which will have...marketing. Serve as a bridge to Nonclinical Development on clinical safety findings, particularly ones likely to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, Global Brand Team, and Global Product ... areas centered around rare diseases and immune disorders.Summary The Senior Director , Global Oncology Medical Affairs is responsible for developing the Global… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …narratives, Provides medical direction to MW for the CSR; Working with Clinical Safety Pharmacovigilance (CSPV), defines product level surveillance plan and ... program in a specific indication, ie, multiple multinational phase II/III clinical trials; Reviews regulatory documents from cross functional, holistic perspective;… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …journalsAssess clinical trial and/or other data sources to contextualize safety events for assigned product. Research natural history of disease to characterize ... centered around rare diseases and immune disorders. SUMMARYThe Associate Director , Pharmacoepidemiology position provides epidemiologic, methodological, and analytic support… more
- Bristol Myers Squibb (Summit, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Director will be the clinical lead to progress early clinical ... Clinical Scientist for medical questions and education (including safety management guidelines) + Assesses key safety -related...+ Advanced degree(s) in relevant field: MD , MD /PhD (or x-US equivalent) and clinical expertise… more
- Bristol Myers Squibb (Summit, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Director will be the clinical lead to progress multiple early ... Safety physicians in the ongoing review of safety data + Provides clinical leadership and...**Leadership and Matrix Management** + May be responsible for managing Early Clinical Development Physicians, attracting, developing… more
- Pfizer (New York, NY)
- …and outcomes research colleagues, Regional and Country medical teams, Global Clinical Development, Medical information, Regulatory, Safety , etc.) to develop ... to the VP, Global Gastroenterology Medical Lead, the Senior Director , Gastroenterology (GI) and Biosimilars is an integral member...medical groups and key opinion leaders to demonstrate the clinical value of the Pfizer Biosimilars portfolio in the… more
- Pfizer (New York, NY)
- …work of other colleagues to achieve meaningful outcomes and create business impact. + MD required and 5+ years of clinical experience + Significant industry and ... **ROLE SUMMARY** The Senior Medical Director HQ PAXLOVID Team Lead reports to the...and researchers as appropriate + Supports activities related to safety evaluations and reporting requirements. + Responsible for leading,… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …researching on real-world evidence, and creating hope for all facing illness. The Director , Clinical Science (I&I) will lead the early- to late-stage development ... and requirements, both local and international, related to the clinical medicine and drug development processes. The Director...senior management on a global basis. + Supports regulatory safety reporting for clinical programs as needed:… more
- Intra-Cellular Therapies, Inc (New York, NY)
- …demand integrity and respect in all we do, create and deliver. The Associate Director / Director Clinical Development, will be responsible for the leadership, ... origin, protected veteran status, disability or any other legally protected status. Associate Director Clinical Development Base Salary range $175K - $190K … more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …help create possible, together. **Job Description** + Serves as a senior scientific and clinical expert for safety profile of products in therapeutic areas + ... signals and trends, and supports management of any potential safety issues Essential Duties: + Oversees clinical ...Leads a portion of BLA submission activities. Requirements: + MD / DO / Pharm D degree or equivalent. Completion… more
- Merck (Rahway, NJ)
- …and dedicated colleagues while developing and expanding your career. The Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will... trials (design, operational plans, settings) based on these clinical development strategies + Monitoring and managing … more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …into the Senior Director of the Translational Medicine (TM) group, the Director , TM will lead clinical and scientific aspects of translational studies from ... (edaravone) oral suspension in 2022. The company handles research, clinical development, sales, marketing, medical affairs, and business development functions.… more
