- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Summary** The Associate Director of Regulatory Writing is a key role responsible for ... strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of BLA/MAA submissions, working… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …exciting and unique opportunity for a medical writer to join our dynamic team at the Associate Director level. You will author a wide range of regulatory ... content that is used for a variety of purposes, including critical regulatory submissions. Medical Writing collaborates cross-functionally to advance Gilead's… more
- CBRE (New York, NY)
- ESG Process and Controls Associate Director Job ID 201478 Posted 22-Jan-2025 Service line Corporate Segment Role type Full-time Areas of Interest ... The Role:** As a CBRE ESG Process and Controls Associate Director , you will be part of...robust ESG processes, mitigate risks, and ensure compliance with regulatory requirements. **What You'll Do:** + Develop and implement… more
- Taiho Oncology (Princeton, NJ)
- …and execution, analysis and reporting of data, and authoring/review of scientific and regulatory documents. The Associate Director of Biostatistics will have ... Associate Director , Biostatistics Princeton, NJ, USA...clinical data + Create/author statistical sections of scientific and/or regulatory documents + Manage external biostatisticians to ensure quality… more
- Sanofi Group (Bridgewater, NJ)
- **Job title** : Associate Director , Global Oncology Corporate Communications **Location:** Cambridge, MA 50% remote working; limited travel expected. **About the ... the world. Sanofi is looking for a proactive, high-energy Associate Director to join the Global Specialty...global communications programming in support of clinical data and regulatory milestones as well as pipeline; 2) supporting development… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …on real-world evidence, and creating hope for all facing illness. The Associate Director , Biostatistics is responsible for providing statistical support to ... deliverables for contracted statistical services. + Provides statistical components of regulatory submissions. + Assists the Department Head in the preparation of… more
- TIAA (New York, NY)
- ** Associate General Counsel** The Director , Associate General Counsel will join a team responsible for providing legal advice and strategic guidance for ... TIAA India, and other key partners on new laws and regulatory developments, including those applicable to marketing, communications, digital experiences, educational… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …on real-world evidence, and creating hope for all facing illness. The Associate Director , Statistical Programming is responsible for building and maintaining ... programming requirements in the preparation of documents for submission to regulatory authorities, including but not limited to, Investigational Drug Applications… more
- Bristol Myers Squibb (Princeton, NJ)
- …Responsibilities: + Develops expertise beyond biostatistics by researching medical literature, regulatory and HTA documents to develop an understanding of the ... clinical, regulatory /HTA and commercial climate. + Contributes to preparation of...data manipulation, graphing & simulation. + Great interpersonal, communication, writing and organizational skills. + Expertise in statistical/clinical trials… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile. - CRO / Vendor ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
- Merck (Rahway, NJ)
- …, Operations, Non-clinical, Clinical, and other functional areas + Experience with regulatory submissions including writing / review of regulatory ... oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team… more
- Merck (Rahway, NJ)
- …, Operations, Non-clinical, Clinical, and other functional areas + Experience with regulatory submissions including writing / review of regulatory ... portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team… more
- Research Foundation CUNY (New York, NY)
- …Programs (GSP) Office of the CUNY School of Medicine and Reporting to the Associate Dean for Research, the GSP Director manages and supports full-time staff ... Job Title: Director of Grants & Sponsored Programs PVN ID:...and works closely with the Associate Dean for Clinical Administration, Finance, & Strategy to… more
- CUNY (New York, NY)
- …closely reflect the diversity of our student body. Under the supervision of the Associate Dean for Research, the Director of Research Programs manages and ... Director of Research Programs **POSITION DETAILS** The CUNY...supports full-time staff and works closely with the Associate Dean for Clinical Administration, Finance, & Strategy to… more
- PSEG (Newark, NJ)
- …as the attention, camaraderie, and care for one another you might typically associate with a small business. Our focus on combatting climate change through clean ... internal controls and maintenance of tax accounting related databases. In addition, the Director - Tax Accounting and Reporting collaborates with the Director of… more
- Merck (Rahway, NJ)
- **Job Description** The Executive Director , Global Pharma Communications is responsible for leading, developing and executing US and global communications strategies ... infectious diseases, neuroscience, ophthalmology, and immunology. Reporting to the Associate Vice President, Human Health and Manufacturing Communications, the… more
- TD Bank (New York, NY)
- …advisory support to fixed income sales and trading businesses. + Provide regulatory advice for the municipal securities business, both origination and secondary ... trading. + Provide regulatory advice on a wide range of issues including...a diverse range of financial products knowledge and strong writing and research skills. The successful candidate will have… more
- City of New York (New York, NY)
- …which the Board has a short window of time to issue a determination. The Associate will assist the Director of Appeals with handling visit restriction complaints ... in-person interview will be required to complete a brief writing and analysis assignment and will be asked for...Only candidates under consideration will be contacted. The Legal Associate (" Associate ") will report directly to, and… more
- Mount Sinai Health System (New York, NY)
- …and monitors all safety aspects of clinical research trial(s). Under guidance of the Associate Director of Research and Quality Outcomes, the CRA is responsible ... studies as a clinical trial assistant or clinical research associate is desired. + Excellent Communication and writing...for adjudication by the CEC. + Participates with the Director of Research and Quality Outcomes in the preparation,… more
- Merck (Rahway, NJ)
- …modeling, Quality by Design (QbD) and Lean Six Sigma principles. + Experience supporting/ writing regulatory filings (IND, MAA, BLA) and inspections with multiple ... manufacturing sites, manufacturing investigations, process validation, and authoring of regulatory submissions. Under the general scientific and administrative direction… more