- 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 ... a plus + international MD is okay + 1-3 years of Pharmacovigilance (PV)/ clinical safety experience in pharmaceutical drugs either from relevant work experience… 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...and GCP guidelines as well as applicable SOPs regarding clinical safety + Possesses proficient scientific expertise… more
- Bristol Myers Squibb (Princeton, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Clinical Data Standards is a leadership role ... This role reports to Director or Executive Director , Head Standards Management & Steward within Clinical & Safety Data Insights and Analytics. **Position… more
- AbbVie (Branchburg, NJ)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Clinical Development will have global or ... Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director ,...or risks (eg, changes or significant risks to the Clinical Development Plan, new safety concerns) upon… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Scientist reports through the Clinical Science function which ... provides scientific expertise necessary to design and deliver clinical studies and programs. **Position Summary / Objective** + Responsible for implementation,… more
- Mount Sinai Health System (New York, NY)
- … safety aspects of clinical research trial(s). Under guidance of the Associate Director of Research and Quality Outcomes, the CRA is responsible for ... **Job Description** The Clinical Research Associate is an integral...as assigned. ** Safety Reporting:** + Assists the Associate Director of Research and Quality Outcomes… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Safety Scientist in... (GPS) will play a key scientific role in safety strategies for molecules in clinical development and ... post-marketing phases, under the guidance of the safety lead. This will include review, analysis and interpretation of safety data (including aggregate data) to… more
- Merck (Rahway, NJ)
- **Job Description** Under minimal guidance of the Executive Director / Director / Associate Director , Pharmacovigilance (PV) Partner Strategy & Management ... and vendor PV agreements and leadership of the Global Clinical Safety & Pharmacovigilance (GCS&PV) implementation activities...and SMPs. + Maintains, in collaboration with the Executive Director / Director / Associate Director … more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …of bipolar depression in adults as monotherapy and as adjunctive therapy. The Associate Director / Director of Medical Writing provides support for the ... documents, Regulatory documents, and responses to health authority information requests. The Associate Director / Director of Medical Writing must have… more
- AbbVie (Florham Park, NJ)
- …level will be determined by the qualifications listed below. Purpose: The Associate Scientific Director , Psychiatry Pipeline role provides medical and scientific ... projects, etc.) at the regional/local level. + Participation in design and execution of clinical trial safety , product safety and risk management plans.… more
- AbbVie (Florham Park, NJ)
- …pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for ... and other program documents. *May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical... Associate Medical and/or Scientific Directors, and of Clinical Scientists working on the same or related programs.… more
- AbbVie (Florham Park, NJ)
- …level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational ... practice standards, including regulatory guidelines to meet customer needs. Qualifications Associate Scientific Director Qualifications + Bachelor's Degree in… more
- Bristol Myers Squibb (Princeton, NJ)
- …by leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... for managing the end-to-end process for IC for BMS-sponsored clinical trials. This includes a centralized triage function for... Director of Informed Consent Management. The AD will be… more
- Mount Sinai Health System (Long Island City, NY)
- **Job Description** The Associate Director of Nursing is responsible for the management and oversight of nursing practice for assigned clinical areas. S/he ... compliance with contractual agreements, and supports positive employee-management relationships. The Associate Director of Nursing is responsible for the… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …internally in the kilolab and externally at contract manufactures. + The Associate Director will have organizational and interdepartmental responsibilities with ... filings to bring these novel medicines to patients worldwide. **Position Summary:** The Associate Scientific Director will be an engineering lead or project… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... you will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department… more
- J&J Family of Companies (Raritan, NJ)
- Associate Director , Signal Detection Scientist - 2406212640W **Description** Johnson and Johnson is currently seeking an ** Associate Director , Signal ... drug safety or related area and 1 year of clinical /patient-care experience highly preferred **Required:** * Understanding of global health authority regulations… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director will lead the execution and lifecycle management of ... Global Medical Affairs' externally sponsored clinical research (ESR) initiatives, ensuring strict...partners, promoting a cohesive team approach. + Regulatory and Safety Compliance: Understand study conduct from supply chain/drug forecasting… more
- Merck (Rahway, NJ)
- **Job Description** ** Associate Director , IT Research Automation Engineer in RaDS** **IT** RaDS IT Research Infrastructure Product Line (RIPL) engineering team ... is seeking an Associate Director - Research Laboratory Automation Engineer....expansion, efficiency and productivity across drug discovery modalities and clinical phases. You will collaborate with multidisciplinary organizations in… more