- Merck & Co. (Rahway, NJ)
- …Our company's oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle ... placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May Be Responsible ForEvaluating pre- clinical and… 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. (Bernards, 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primary source of medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the internal and external network ... medical input regarding country feasibility. Consulted on decisions related to clinical trial feasibility and contributes to the site feasibility assessment from… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization ... of clinical sections of study-level documents (eg, protocol, amendments)Reviews safety data to mitigate risk to trial participants for the assigned trial… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …this role, the incumbent will contribute to creation and improvement of Clinical Development processes. Job Description:Execute an overarching safety program ... and in the real-world setting.Contributes to creation and improvement of Clinical Development processes. Education: MD required; prefer Board certification in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …function as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US ... compound under the supervision and leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical...Product Team to inform clinical development, commercialization, market access, and other cross-functional strategic… more
- Actalent (Basking Ridge, NJ)
- Job Title: Director , Clinical SafetyJob Description The Director , Clinical Safety , will be a product safety lead or part of a product safety ... safety surveillance and risk management. This role provides safety leadership, including but not limited to clinical... safety monitoring and risk management through the Safety Management Team framework. The Director will… more
- System One (Basking Ridge, NJ)
- Associate Director , Clinical Safety MD Pharma In New Jersey - Remote (no west coast, only EST or CST) 12 month contract | Up to $100/hr dependent on ... MD is okay + 1-3 years of Pharmacovigilance (PV)/ clinical safety experience in pharmaceutical drugs either...collaborate with others + Safety experience in clinical development preferred Education : Education: MD /DO… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …around rare diseases and immune disorders. **Summary** This 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
- Bristol Myers Squibb (Summit, NJ)
- …with the Clinical Scientist for medical questions and education (including safety management guidelines) + Assesses key safety -related serious adverse events ... oversight in protocol development (input on inclusion/exclusion and other safety -related clinical considerations) + Fulfills GCP and...+ Advanced degree(s) in relevant field: MD , MD /PhD (or x-US equivalent) and clinical expertise… more
- Pfizer (New York, NY)
- …+ Research: + Develop strategies and manage Investigator-Initiated Research program, Clinical Research Collaborations and analyses of Real World Data. + Publication ... Subcommittee (PSC) Membership: + Collaborate with Clinical Development and Global colleagues on key governance committee to support development of strategic global… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Senior Medical Director , Clinical Sciences, Hematology provides clinical leadership and is responsible for all clinical deliverables within the ... clinical program with minimal supervision from Program Lead MD . Clinical deliverables may include individual protocols...HE&OR), and internal decision boards. + Supports Program Lead MD in ensuring overall safety of the… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Director Clinical Development - Oncology Date: Sep 13, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 58170 ... clinical programs worldwide across all phases of clinical research. The Director will oversee study...experience in a pharmaceutical industry environment or related area planning/ managing clinical trials, with proven ability to… more
- Merck (Rahway, NJ)
- **Job Description** The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving ... in Immunology. With a focus on late-stage development, the Clinical Director will manage the entire cycle... trials (design, operational plans, settings) based on these clinical development strategies + Monitoring and managing … more
- Teva Pharmaceuticals (Parsippany, NJ)
- Director Clinical Development Date: Sep 29, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 57466 **Who we ... be based in Parsippany, NJ or West Chester, PA Director , Clinical Development is responsible for the...experience in a pharmaceutical industry environment or related area planning/ managing clinical trials, with proven ability to… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads...and GCP guidelines as well as applicable SOPs regarding clinical safety + Possesses proficient scientific expertise… more
- Sanofi Group (Morristown, NJ)
- ** Director Clinical Development** **Location: Swiftwater, PA, Cambridge, MA, Orlando, FL or Morristown, NJ site (flexibility with US site)** **About the job** We ... impact on millions of patients around the world. The Director Clinical Development is the clinical...operate. + Establishes the conditions essential for determining the safety of all subjects involved in Clinical … more
- Pfizer (New York, NY)
- …for. + Serves as a Medically Qualified Individual (MQI) at Pfizer, reviewing clinical trial data for safety signal identification and tracking. + Provides ... of clinical research studies, in conjunction with the Development Director , Operations Manager, and Clinician; accountable for final decision. + Establishes… more
- Hackensack Meridian Health (Edison, NJ)
- …to transform healthcare and serve as a leader of positive change. The ** Director , Member Scientist, Clinical Research** is responsible for initiating, leading ... research in brain injury. **Responsibilities** A day in the life of a ** Director , Member Scientist, Clinical Research** at Hackensack Meridian _Health_ includes:… more
