- Takeda Pharmaceuticals (Columbus, OH)
- …innovation-driven company to inspire you and empower you to shine? Join us as an Associate Director , GCP Compliance based remotely reporting to the ... Director , GCP Compliance. At Takeda, we are transforming the pharmaceutical...+ Develop, lead and oversee compliance assessments to address GCP Quality Plan, CAPAs/ECs and liaise with… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Associate Director , Education and Quality Assurance (Abramson Cancer Center) ... Job Profile Title Associate Director , Clinical Research Quality Job Description Summary...oversight that is aligned with ICH Good Clinical Practice ( GCP ) to ensure ACC CRU inspection readiness comply with… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Global Clinical Quality Date: Nov 21, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job ... risk management activities, and leads continuous improvement for clinical development activities. The Associate Director - Global Clinical Quality leads a… more
- Vera Therapeutics (Brisbane, CA)
- Title: Associate Director , Quality Assurance Location: Brisbane, CA About Us: Vera Therapeutics (Nasdaq: VERA), is a late-stage biotechnology company focused ... suffering from immunological diseases. Position Summary: We seek an Associate Director , Quality Assurance to...be responsible for developing and maintaining GMP, GLP and GCP Quality Management Systems in accordance with… more
- BeiGene (San Mateo, CA)
- **General Description:** The Associate Director of R&D Quality Systems, Strategy, and Excellence (Strategy & Innovation) is responsible for leading ... quality outcomes and enhance decision-making processes. The Associate Director will drive cultural change and...Build and maintain strong cross-functional partnerships across GxP areas ( GCP , GMP, GVP) to ensure alignment in quality… more
- Kedrion Biopharma (Atlanta, GA)
- …as well as answering any questions you may have! **Position Overview** The Associate Scientific Director , Clinical Development, serves as a Clinical Scientist ... may act as a delegate of the Therapeutic Area Lead or Medical Director for clinical development programs. This role ensures patient safety, compliance with company… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the ... of study data of a clinical development program. The Associate Director leads in a matrix environment...maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
- Penn Medicine (Plainsboro, NJ)
- …future each day. Are you living your life's work? We are hiring for an Associate Director Oncology Research Operations to join our Cancer Services team at Penn ... This individual must have oncology healthcare research expereince. Summary: + The Associate Director Oncology Research Operations reports directly to the … more
- Frontier Medicines (South San Francisco, CA)
- Frontier Medicines is seeking a highly motivated individual to fill the position of Associate Director of Clinical Operations to help develop the early project ... development. The position will report to the CMO. The Associate Director , Clinical Operations will be a...delivery of the assigned clinical programs in compliance with quality standards (including ICH GCP , local regulations)… more
- AbbVie (North Chicago, IL)
- …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Global Site Management (AD, GSM) reports into ... the Therapeutic Area (TA) Director , Global Site Management and is responsible for managing...CSM in a world class manner, ensuring compliance and quality . + Collaborates with other GSM Associate … more
- Lilly (Indianapolis, IN)
- …ensures the on-time delivery of solutions that are aligned to business processes. The Associate Director ensures quality practices are in place around ... and guidance to speed the delivery of medicines to patients globally. The Associate Director - Clinical Results Reporting Systems role requires broad expertise… more
- System One (King Of Prussia, PA)
- Title: Associate Medical Coding Director Full Time Permanent Opportunity - Direct with the client Onsite King Of Prussia, PA SUMMARY/JOB PURPOSE: The ... Associate Medical Coding Director is responsible for the delivery of timely and quality coding deliverables for clinical trials and programs. This position… more
- Lilly (IN)
- …to operationalize these trials and enable asset strategies across the portfolio. The Associate Director of CCSI is passionate about delivering the implementation ... (eg, FDA, ICH), Quality and Business Systems, and Good Clinical Practices ( GCP ) to achieve inspection readiness and detect and resolve quality issues. +… more
- Takeda Pharmaceuticals (Boston, MA)
- …Management and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs ... of my knowledge. **Job Description** **OBJECTIVES:** + Ensures Global and R&D Quality processes are embedded and effectively implemented across CPMQ + Partner with… more
- Conviva (Columbus, OH)
- …a part of our caring community and help us put health first** The Associate Director , Security Architecture will play a key role in implementing security ... the enterprise can achieve the enterprise security strategy. The Associate Director , Security Architecture will play a...cyber security architecture experience architecting cloud solutions in Azure, GCP or AWS + 7 or more years of… more
- Bristol Myers Squibb (Madison, NJ)
- …by leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... Director of Informed Consent Management. The AD will be...teams across BMS to ensure both patient safety and quality , and specimen and data compliance. + Independently liaise… more
- Actalent (Conshohocken, PA)
- Job Title: Associate Director of Medical Affairs OperationsJob Description The Associate Director of Medical Affairs Operations will be accountable for ... are delivered on time, within budget, and with high quality . This role involves managing relationships with external study...affairs, investigator sponsor trials (IST), and good clinical practice ( GCP ). + Knowledge of ICH, GDP, CFR, and systems… more
- Bristol Myers Squibb (Madison, NJ)
- …centralized monitoring for trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a leadership role with ... the BMS R&D pipeline. This role reports to the Director , External Data Acquisition within GDM and is a...maximize their potential. Empowering and holding staff to high quality performance and delivery. + Ensuring procedural documents are… more
- Takeda Pharmaceuticals (Columbus, OH)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Signal Management Process Excellence in Cambridge, MA, where ... implement process excellence strategies to enhance the efficiency and quality of signal management activities. As part of the...Innovation (SMI) team, you will report to the Senior Director , Head, Signal Management and Innovation (SMI). You will… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Associate Director , Vendor Management, is responsible for assessing, onboarding, and overseeing the health and performance of vendors involved in clinical ... compliance standards, manage relationships, and oversee delivery to time, cost, and quality . This position is capable of leadership and oversight of vendor segments,… more
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