- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Management (RPM) provides planning and drives coordination of global and US regulatory activities. The Associate Director RPM is responsible for ... centered around rare diseases and immune disorders. Summary: The Associate Director , Regulatory Affairs -...supporting the global regulatory lead (GRL), US regulatory lead (USRL) and global … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …US or EU. Preparation of updated Core Data Sheets, and EU and US Documentation: Independently manages, prepares and implements regulatory documents (eg, USPI, ... Years pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …robust development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory ... the company's growth, thereby accomplishing corporate goals.ResponsibilitiesDevelop and implement US regulatory strategy for assigned project(s).Strategize and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …quality standards and timelines and that quality of data is suitable for regulatory submission.The Associate Director will have routine interaction with ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …include management of all day-to-day payroll operations and activities for all US (multi-state) and Canada regions, ensuring compliance with company policies and ... Tax, Compliance and Legal team members to ensure compliance with all relevant regulatory , accounting, tax and internal requirements. This person leads the timely and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and programs to support the business functions of Daiichi Sankyo (DS) in the US , EU, Japan, and other global sites. These business functions include but are not ... to Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Management (RPM) provides planning and drives coordination of global and US regulatory activities. The Associate Director RPM is responsible for ... centered around rare diseases and immune disorders. **Summary:** The Associate Director , Regulatory Affairs -...supporting the global regulatory lead (GRL), US regulatory lead (USRL) and global … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …robust development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory ... growth, thereby accomplishing corporate goals. **Responsibilities** + Develop and implement US regulatory strategy for assigned project(s). + Strategize and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …US or EU. Preparation of updated Core Data Sheets, and EU and US Documentation: Independently manages, prepares and implements regulatory documents (eg, USPI, ... industry experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + Experience with ex- US … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …agreed quality standards and timelines and that quality of data is suitable for regulatory submission. The Associate Director will have routine interaction ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and… more
- J&J Family of Companies (Raritan, NJ)
- Johnson & Johnson Innovative Medicine is recruiting for Associate Director , RA Submissions. The position can be located on-site/hybrid in the US (Titusville, ... health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are...in this posting applies to candidates hired in the United States . Candidates hired outside the … more
- Sanofi Group (Bridgewater, NJ)
- **Job Title:** Associate Director , Consumer Marketing - US Rare Hematology **Location** : Cambridge, MA **_About the Job_** This role will drive consumer ... is based in Cambridge, MA and will report into Director of Consumer marketing for rare hematology. We are...experience in the pharmaceutical or biopharmaceutical industries. + Prior US launch experience is strong desired. + Fostering strong… more
- AbbVie (Branchburg, NJ)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Clinical Development will have global or regional ... position may be based in Branchburg, NJ or Irvine, CA. Responsibilities: The Associate Director will be responsible and accountable for the development,… more
- Lilly (Branchburg, NJ)
- …Lilly and Active Pharmaceutical Ingredient (API) Contract Manufacturer representatives. The JPT Associate Director is the key business relationship owner and is ... materials are delivered on time and within downstream customer expectations. The JPT Associate Director will partner with Lilly's Process Research & Development… 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
- Sanofi Group (Bridgewater, NJ)
- **Job Title:** Associate Director , Global Oncology Franchise Operations **Location** : Bridgewater, NJ or Cambridge, MA The Associate Director , Global ... the Sanofi Hubs + Execute congress activities in compliance with medical, regulatory and legal requirements **Other: 30%** Additionally, this person will assist in… more
- Sunrise Senior Living (Basking Ridge, NJ)
- …**COMMUNITY NAME** Sunrise of Basking Ridge **Job ID** 2024-220603 **JOB OVERVIEW** The Associate Director of Sales (ADOS) is responsible for supporting and ... duties the ADOS may, under the supervision of the Director of Sales (DOS), Director of Sales...resident's Administrative File according to Sunrise and state specific regulatory requirements. + Manages the move-in process as outlined… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Vendor Management, is responsible for assessing, onboarding, and overseeing the health and performance of vendors involved in clinical ... Quality and Compliance Oversight: + Ensure vendors comply with regulatory requirements and organizational standards, including proper documentation of partnerships… more
- Amneal Pharmaceuticals (Piscataway, NJ)
- …The Associate II (A), assists with minimal guidance, the Senior Director of Regulatory Affairs Clinical/ FDA Communications.Assists the Senior Director ... the daily FDA communications/ updates Essential Functions: + Assist the Senior Director of Clinical Regulatory Affairs/ FDA Communications in managing,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and programs to support the business functions of Daiichi Sankyo (DS) in the US , EU, Japan, and other global sites. These business functions include but are not ... to Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance,… more
