- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research ... Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle... trials (design, operational plans, settings) based on these clinical development strategiesMonitoring and managing the conduct… more
- Tris Pharma (Monmouth Junction, NJ)
- …Monmouth Junction, NJ facility for an experienced MD to serve as Senior Director or Director , Clinical Development. Title and salary commensurate with ... experience. The position is a core member of the Clinical Development management team responsible for developing and implementing, in alignment with corporate… 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 ... placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be responsible for:-Evaluating 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 Senior Director will manage the entire cycle ... placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director may be responsible for:Evaluating pre- clinical and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …publications strongly preferred 4+ years Pharmaceutical/Biotech industry experience, including time managing clinical trials, or academic clinical research ... new medicines for patients. The Position As Senior Medical Director for the liver disease team, you will be...clinical trials, the drafting of medical/ scientific documents, safety monitoring, and data analyses. In this high visibility… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …internal and external stakeholders. Relationships This position will report to Senior Global Safety Lead/ Director /Senior Director - Safety Surveillance, ... committees: Participate as a member of the first safety committee chaired by non- clinical , where ...project. Physical Requirements Approximately 10% overnight travel required. Qualifications MD or PhD or equivalent degree with 8+ years… more
- Genmab (Plainsboro, NJ)
- …is essential to fulfilling our purpose. The Role: The Senior Medical Director supports Oncology Clinical Devlopment. Responsibilities: Oversee clinical ... Oversee safety of the drug, including the safety aspects of patients in clinical studies...other relevant fora to maintain up-to-date scientific/medical knowledge Requirements: MD background with a minimum of 10+ years of… more
- Merck (Rahway, NJ)
- **Job Description** The **Senior Clinical Director (Sr. Principal Scientist)** has primary responsibility for the strategic planning and directing clinical ... Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle... trials (design, operational plans, settings) based on these clinical development strategies + Monitoring and managing … more
- Danaher Corporation (New York, NY)
- …lives with diagnostic tools that address the world's biggest health challenges. The Senior Director of Medical Safety and Compliance will lead the Medical ... role is crucial in maintaining high standards of medical safety , compliance, and regulatory adherence at Beckman Coulter Diagnostics....The essential requirements of the job include: + Physician ( MD or equivalent) + 6+ years of clinical… more
- The Mount Sinai Health System (New York, NY)
- …Research Associate is an integral part of the research study team and monitors all safety aspects of clinical research trial(s). Under guidance of the Associate ... for collecting, assessing and processing Adverse Events (SAE) for safety reporting, CEC and DSMB of clinical ...implements plans as required. + Additional duties as assigned. ** Safety Reporting:** + Assists the Associate Director … more
- Merck (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
- Novo Nordisk (Plainsboro, NJ)
- …and execution of clinical trials, the drafting of medical/ scientific documents, safety monitoring, and data analyses. The Medical Director will also assist ... equivalent is required + 1+ years Pharmaceutical/Biotech industry experience, including time managing clinical trials, or academic clinical research… more
- Merck (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 ... placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director may be responsible for: + Evaluating pre- clinical and… more
- Merck (Rahway, NJ)
- …**Position Title** - Principal Scientist **Department** - Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease **Brief Description of ... contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS....10% **Qualifications, Skills & Experience** **Education Minimum Requirements:** + MD or Ph.D. or other related doctoral degree in… more
- The Mount Sinai Health System (New York, NY)
- **JOB DESCRIPTION** The Senior Director - Actuary collaborates with stakeholders from across the organization and leads a team of directors and/or analysts to ... decision-making, goal setting, and effective performance measurement. The Senior Director - Actuary will be a leader in the...Care and/or Population Health contracts, including the impact of clinical interventions on total cost of care. * Develop… more
- Pfizer (New York, NY)
- **ROLE SUMMARY** This position will be responsible for supporting a late-stage clinical trial. The successful candidate should ideally have prior experience in ... clinical trials and supporting development programs. **ROLE RESPONSIBILITIES** +...manuscripts, abstracts and presentations for scientific meetings + Evaluate safety , pharmacology, and efficacy data from ongoing and completed… 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
- The Mount Sinai Health System (New York, NY)
- …if a secondary review is required to verify assignment of Patient Safety Indicators, HAC, Clinical Documentation Improvement,Sepsis and any other charts ... requirements. The CRM works in conjunction with the Associate Director and Director of DRG Validation to...meeting criteria for secondary review. Initiates an MD query to clarify documentation in the medical record… more
- Novo Nordisk (Plainsboro, NJ)
- …internal and external stakeholders. Relationships This position will report to Senior Global Safety Lead/ Director /Senior Director - Safety Surveillance, ... committees: + Participate as a member of the first safety committee chaired by non- clinical , where ...Physical Requirements Approximately 10% overnight travel required. Qualifications + MD or PhD or equivalent degree with 8+ years… more
- Merck (Rahway, NJ)
- **Job Description** ** Clinical Safety and Risk Management (CSRM)** ** Director / Principal Scientist** **Description:** Under the general direction of an ... Executive Director , General Medicine, the CSRM Principal Scientist is a leader in drug safety and is responsible for overall clinical risk management and … more
