- 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
- 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
- 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
- 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
- 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 (Titusville, 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
- Bristol Myers Squibb (Princeton, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning, study results… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... and executes a labeling implementation plan to incorporate new scientific, safety and clinical data, as well as Health Authority responses / feedback into… more
- Novo Nordisk (Plainsboro, NJ)
- …internal and external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key internal ... management of Senior Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate...committees + Participate as a member of the first safety committee chaired by non- clinical , where … more
- Bristol Myers Squibb (Princeton, NJ)
- …Read more: careers.bms.com/working-with-us . This is a Hybrid role Nonclinical Safety (NCS), within Nonclinical Research and Biotherapeutics, is responsible for ... designing and implementing overall nonclinical safety strategy to support the development and eventual marketing...INDs and NDAs, IBs, PIPs, briefing books to support clinical trials and drug registration globally. + Participates in… more
- Bristol Myers Squibb (Princeton, NJ)
- …shifting priorities. **Key Responsibilities** + In partnership with the Senior Director , Supplier Quality Excellence, Global Supplier Compliance Leads and the Vendor ... and technology solutions. + Promote and enable a culture of psychological safety , inclusion, and diversity. + Champion an Enterprise-wide Quality mindset / Culture… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, ... Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services, Project Management and Operational Management. Develop a strong, positive strategic business partnership with the global R&D business and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core ... Data Sheets (CCDS) for assigned products. This position drives/leads the maintenance of global labeling and associated documents (including cartons and external packaging in the US) for assigned Daiichi Sankyo products. This position ensures that draft… more
- Gentiva (Hamilton, NJ)
- … Director , Hospice Branch Director , Director of Operations, DON, Director of Nursing, Director of Clinical Operations, Home health administrator, ... have an exciting and rewarding opening for an **Executive Director - RN** to join our team in Hamilton...leadership teams in the industry where a focus on clinical excellence, exemplary patient care, employee recognition and satisfaction… more
- BluePearl (Langhorne, PA)
- …a collaborative, engaged, and passionate veterinary leader with several years of clinical experience to lead our team of emergency and specialty clinicians in ... the role of **Medical Director ** . The Medical Director will partner...(patient care, client and referral veterinarian satisfaction, and patient safety ), **supporting quality and operational initiatives, fostering a clinician-driven… more