- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director /Principal Medical Writer **Location:** Cambridge, MA Morristown, NJ **About the Job** Are you ready to shape the future of ... who has an extensive experience with the preparation of clinical documents and regulatory dossiers and has demonstrated leadership skills as submission lead. As an… more
- AbbVie (Florham Park, NJ)
- …will be based on qualifications listed below. Purpose: The Scientific/Medical Director , Medical Affairs provides specialist medical and scientific strategic and ... scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. + Has overall responsibility for oversight… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …or external reviews including ensuring alignment with Gilead business needs and regulatory requirements. + Stay current with evolving global PV regulations ... audits, in the biopharma or related industry. + Proficiency in pharmacovigilance regulatory requirements ( Global ) is a must. + Expert-level experience working… more
- Sysco (Rahway, NJ)
- …regulatory requirements in domestic and international markets. + Stay current on global regulatory trends; assess potential impact and ensure timely alignment ... building a high-performing quality culture across the organization. **POSITION PURPOSE:** The Director of Global Quality Assurance & Quality Control leads the… more
- Sumitomo Pharma (Trenton, NJ)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... seeking a dynamic, highly motivated, and experienced individual for the position of ** Director , Patient & HUB Operations, Rare Disease** . The Director , Patient… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are seeking a Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, ... study data of a clinical development program. The Associate Director leads in a matrix environment as part of...other departments; Member of the Clinical Study Team and Global Clinical SubTeam + Maintains proficient understanding of therapeutic… more
- Fiserv (Berkeley Heights, NJ)
- **Calling all innovators - find your future at Fiserv.** We're Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves ... If you want to make an impact on a global scale, come make a difference at Fiserv. **Job...scale, come make a difference at Fiserv. **Job Title** Director FCC, Emerging Markets **What does a successful … more
- Bristol Myers Squibb (Princeton, NJ)
- …development including analytical validation, clinical development, manufacturing, US and global regulatory submission, and commercialization of diagnostics. ... medicine and R&D. We have an exciting opportunity for a Senior Director to join the Precision Medicine, Bioanalytical and Translational Sciences organization, where… more
- Bayer (Whippany, NJ)
- … packages, regulatory exchanges and data therein; + Understanding of global pharmaceutical regulatory requirements, data standards (eg, IDMP, XEVMPD, SPOR), ... to make a real difference, there's only one choice.** ** Director R&D Reg Data Mgmt Expert DSAI** **YOUR TASKS...management with an initial specific focus on product and regulatory data. This role has broad accountabilities for the… more
- Grifols Shared Services North America, Inc (Atlantic City, NJ)
- …Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being ... more than 110 countries and regions. The primary responsibility of the MSL Field Director is the management, performance, and coaching of a team of MSL direct… more