- Takeda (Boston, MA)
- …application is true to the best of my knowledge. Job Description ABOUT THE ROLE The Associate Director , GCP Audit & Compliance provides strategic quality ... adherence to GCP , GCLP, and GVP standards. This role combines audit leadership, supplier oversight, and strategic risk management to enhance end-to-end clinical… more
- Takeda (Boston, MA)
- A global pharmaceutical company is seeking an Associate Director for GCP Audit & Compliance in Boston, MA. This role involves leading quality oversight ... for clinical and pharmacovigilance suppliers, conducting audits, and ensuring compliance with regulatory standards. The ideal candidate has over 15 years of relevant experience and a strong background in quality management and regulations. The position offers… more
- Shionogi Inc. in (Florham Park, NJ)
- Overview The Associate Director , GCP /GVP Quality Assurance provides senior-level quality oversight for Shionogi's clinical development and pharmacovigilance ... (PSMF). Working with cross-functional partners and external vendors, the Associate Director drives risk mitigation strategies to...clinical trial and PV operations. Develop and ensure the GCP and GVP audit plan(s) is(are) executed… more
- Exelixis, Inc. (Alameda, CA)
- Associate GCP /GLP QA Director page is loaded## Associate GCP /GLP QA Directorlocations: Alameda, CAtime type: Full timeposted on: Posted Yesterdayjob ... for Clinical programs. This leader provides insight and partners with both GCP QA staff and Clinical Operations Quality Management (OQM) to address day-to-day… more
- NY CREATES (Albany, NY)
- …epicenter of high-tech innovation and commercialization. Job Description: Job Description for Associate Director of Identity and Access Management JOB SUMMARY ... The Associate Director of Identity and Access Management...labs, semiconductor cleanrooms, HPC clusters, cloud workloads (AWS, Azure, GCP ), OT/ICS environments, and federated partner ecosystems. With elite… more
- Arcus Biosciences, Inc. (Hayward, CA)
- Summary The Associate Director , Clinical Quality Assurance is responsible for working with study management teams to facilitate internal and external adherence ... Compliance by ensuring conformance to domestic and international quality regulations and GCP guidelines. The role is accountable for participating in day‑to‑day QA… more
- Revolution Medicines (Redwood City, CA)
- …in the RAS signaling pathway. The Opportunity Revolution Medicines is seeking an Associate Director , Clinical Quality Assurance, who will play a key role ... of applicable Quality Systems and procedures that comply with applicable GCP standards and guidelines. Collaborate with clinical functions (eg, Clinical Operations,… more
- Gilead Sciences, Inc. (Foster City, CA)
- Associate Director , Quality - Clinical Data Science The Associate Director , Quality will be responsible for designing, implementing, and optimizing ... System (QMS). This role requires an in-depth knowledge of GCP and understanding of regulatory requirements applicable to the...requirements applicable to the conduct of clinical trials. The Associate Director , Quality will partner with key… more
- Takeda (Boston, MA)
- …true to the best of my knowledge. Job Description About the role: The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring the ... CPMQ insights on continuous improvement that are enterprise-wide (ie Veeva, QMS, Enterprise Audit , etc.) to Global Quality and R&D Quality. Present to CPMQ at… more
- Apex Systems (Waltham, MA)
- ## Job Description# Associate Director , Safety Systems* Manage Safety Systems user access, configuration updates, testing, and documentation.* Lead validation, ... of relational databases, SQL, and data migrations.* Solid understanding of GCP /GVP regulations (FDA, EMA, ICH E2B).* Familiarity with PSMF documentation and… more
- A10 Networks (San Jose, CA)
- …next phase of infrastructure evolution where speed, stability, and scalability converge. The Associate Director of IT and Infrastructure will play a pivotal role ... Director , IT and Infrastructure page is loaded## ...patching, upgrades, and end-of-life management* Ensure compliance with security, audit , and operational standards in coordination with the Information… more
- Quetzaltx (Chicago, IL)
- …About the role This is a unique opportunity for a Clinical Trial Associate (CTA). You will be responsible for supporting the execution of clinical activities ... with growing independence. This position will report into the Director of Clinical Operations. What you'll do Work on...and site personnel as needed. Ensure document quality and audit readiness in Trial Master File (TMF) With moderate… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality ... adherence to GCP , GCLP, and GVP standards. This role combines audit leadership, supplier oversight, and strategic risk management to enhance end-to-end clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …through communication of audit results and compliance guidelines. + The Associate Director for Regulatory Affairs will have oversight of regulatory ... of health and wellness programs and resources, and much more. Posted Job Title Associate Director , Regulatory Job Profile Title Associate Director ,… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring ... CPMQ insights on continuous improvement that are enterprise-wide (ie Veeva, QMS, Enterprise Audit , etc.) to Global Quality and R&D Quality. Present to CPMQ at… more
- Humana (Frankfort, KY)
- …part of our caring community and help us put health first** The Associate Director , Database Administration manages and maintains all production and ... of physical data storage, maintenance, access and security administration. The Associate Director , Database Administration requires a solid understanding of… more
- Bristol Myers Squibb (Princeton, NJ)
- …of your application should be directed to Chat with Ripley. R1595700 : Associate Director , Data and Solution Architect Revenue Management Systems **Company:** ... creation and maintenance of technical specifications, process documentation, and SOX/ audit compliance artifacts. + Conduct solution reviews, validate configurations,… more
- S&P Global (Princeton, NJ)
- …Role:** **Grade Level (for internal use):** 12 S&P Global Corporate **The** **Role:** Associate Director - Vulnerability Management **The Team:** You will be ... 27001, or SOC 2, with demonstrated experience in regulatory compliance and audit management + Exceptional leadership and communication skills, with ability to… more
- Bristol Myers Squibb (Princeton, NJ)
- …your application should be directed to Chat with Ripley. R1597973 : Associate Director , Companion Diagnostics & Bioanalysis **Company:** Bristol-Myers Squibb ... method, and data lifecycles; steward validated LIMS/ELN records and audit trails. + Serve as the primary liaison for...of FDA QSMR, GLP, CLIA, CAP, ISO13485, IVDR, and ICH- GCP . + Experience with LIMS and electronic data management… more
- System One (Princeton, NJ)
- Job Title: Associate Director of IT - Life Sciences/Clinical Location: Princeton, NJ (Mostly remote with some onsite collaboration required - only EST candidates ... compliance with CFR Part 11/GxP regulations including documentation, validation, and audit readiness. + Modernize legacy systems and support digital transformation… more
