- Oura (San Francisco, CA)
- …New York) occasionally gather informally at local co-working locations. The AGC, Senior Director of Regulatory Compliance & Privacy will provide strategic legal ... compliance with commercial objectives. What you will do: FDA & Global Regulatory Compliance : + Serve...adherence across the organization. + Partner with the Sr. Director - Global Risk & Asset Protection on investigative… more
- Abbott (Santa Clara, CA)
- …device business units that Leveraged Services team supports. **The Opportunity** The ** Associate Director Regulatory Affairs** will work for our Global ... Regulatory Services division within Leveraged Services. As an Associate Director , the individual is to combine knowledge of scientific, regulatory and business… more
- GRAIL (Durham, NC)
- …support Grail's partnerships with pharmaceutical companies for companion diagnostic (CDx) tests. The Associate Director , Clinical Compliance will play a key ... for both clinical trial and companion diagnostic activities, ensuring consistency and compliance with relevant GCP, CLIA, FDA /IVDR, and other global diagnostic… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the ... meet quality requirements, auditing and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards,… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Global Regulatory Lead (GRL), reporting to the Executive Director , Senior Director or ... strategies for projects in their assigned therapeutic area portfolio. **Responsibilities** The Associate Director will be responsible to: + Develop regulatory… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is responsible for ... Global Regulatory Affairs and Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly complex or multiple… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , DRA Product Labeling will lead and manage the ... ECTD compliant. + Responsible for the labeling section of NDA Annual Reports. **Requirements** Associate Director : + Bachelor's degree with a focus in Biology or… more
- Takeda Pharmaceuticals (Boston, MA)
- …monitor the health of the QMS including the identification of systematic quality compliance risks and implementation of robust mitigation plans + Engage with CPMQ ... continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and support to the CPMQ team… more
- Gilead Sciences, Inc. (Foster City, CA)
- …within the CDS organization to ensure clinical trials are conducted in compliance with Gilead procedures, GCP and applicable global regulations + Analyze trends ... Gilead CDS study team to provide expert advice on compliance issues and risk mitigation actions + Collaborate with...to the conduct of clinical trials and guidelines (eg, FDA , EMA, ICH) and related industry standards and trends… more
- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Description:** The role of Associate Director of US Commercial Regulatory Affairs requires the ... compliance of all promotions with approved labeling and /or FDA guidances + Ensure regulatory compliance with sub part e and 2253 regulations + Lead training… more