- Gilead Sciences, Inc. (Parsippany, NJ)
- …for the successful oversight and completion of a broad spectrum of GCP audit activities and deliverables across large sites, countries, or multiple regions. ... as a primary point-of-contact to assigned R&D groups and advise on: GCP regulatory requirements; relevant Gilead policies and procedures supporting audits and… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …well as maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety + Possesses proficient ... We are seeking a Associate Director to join out Oncology Clinical Development department....Proficient knowledge of clinical development process, regulatory requirements and ICH/ GCP guidelines. Does this sound like you? Apply now… more
- Bausch + Lomb (Trenton, NJ)
- …completion of clinical studies according to applicable regulations and guidance, ICH and GCP , and Bausch & Lomb SOPs within agreed-upon timeframes and budget. Also ... study activities are completed in accordance with applicable regulations and guidance, ICH, GCP and B&L SOPs. + Communicate with relevant global team members, other… more
- Acxiom (Trenton, NJ)
- Acxiom is seeking a highly experienced and visionary Senior Director - MLOps Engineering to spearhead the design and development of scalable MLOps platform to ... leveraging platforms such as Databricks, Snowflake, and other enterprise services on AWS, GCP , and Azure. This role offers the flexibility to be located almost… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …and compliance with applicable regulations and guidelines that ensure sustained GCP /QSR compliance . + **Vendor Management:** Leads and develops systems for ... Summary** We are seeking an experienced and dynamic Executive Director of R&D Global Quality to join our team....to ensure that the business units quality management and compliance program are effective and efficient in identifying, detecting,… more
- Merck (Trenton, NJ)
- **Job Description** **Role Summary** + The Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who ... questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, Research, Scientific Congress Support, and… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …and Standard Operating Procedures to optimize MA functioning in terms of leadership, compliance and productivity. The Director , Medical Affairs, will assist the ... Reporting directly to the business unit Vice President of Medical Affairs, the Director of Medical Affairs has the responsibility to support the VP, Medical Affairs… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** The Associate Director , Good Pharmacovigilance Practice (GVP) Audits, serves as a key role within ... Inspection Management, Patient Safety, and other relevant departments. In partnership with GCP and E-System Audit groups, this role helps shape, communicate, and… more
- Sumitomo Pharma (Trenton, NJ)
- …. **Job Overview** The **Senior Director , Clinical Trials Management** is responsible ... of study documents and plans to ensure adequate controls, aligning with GCP and regulatory requirements for study conduct. They will provide expert input… more
- Sanofi Group (Morristown, NJ)
- **Job title** : Global Medical Director , Evidence Generation - Innovation & Partnerships **Location:** Cambridge, MA, Morristown, NJ **About the Job** Sanofi's ... and best in class therapeutic solutions that address highest unmet needs. The Director for medical epidemiology and RWE in the Next-Gen Immunology franchise will act… more