- Lilly (Indianapolis, IN)
- …to enable clinical development and speed medicines to patients. The Associate Director CTF Product Owner in Trial Management Systems will support operational ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...make life better for people around the world. Purpose: Trial Management Systems as part of Clinical Trial… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Position Description:** The Clinical Trial (CT) Supply Management Associate Director will provide operational ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
- Actalent (Basking Ridge, NJ)
- …This role is primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy. Responsibilities ... experience at a biotech or pharma company. + Hematology experience. + Global trial management experience. + Experience with Phase II/III trials. + BS degree… more
- Bristol Myers Squibb (Princeton, NJ)
- …, this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to build and ... integrate one global compliance program...Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data analytics,… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …is true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Global Publications, mature brands, is a key strategic ... the strategic global publication planning for the assigned programs. The Associate Director , Global Publications works in close collaboration with… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Objectives/Purpose** The Associate Director , Global Publications, Immunology, is a key strategic ... of the comprehensive publication plan. In partnership with cross-functional stakeholders, the Associate Director , Global Publications, Immunology will: + Own… more
- Novo Nordisk (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions + Serve ... About the Department Our East Coast Global Development Hub brings together the best minds...FDA + Experience with rare disease drug development, innovative trial design and/or expedited regulatory pathways, highly desired +… more
- 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 , ... people to work towards their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, and work toward excellence in… more
- Bristol Myers Squibb (Princeton, NJ)
- …centralized monitoring for trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a leadership role with ... Global Data Management (GDM) is responsible for clinical trial data acquisition, data standards governance, data management, medical...the BMS R&D pipeline. This role reports to the Director , External Data Acquisition within GDM and is a… more
- Kedrion Biopharma (Atlanta, GA)
- **Position Overview** The Associate Scientific Director , Clinical Development, serves as a Clinical Scientist and may act as a delegate of the Therapeutic Area ... Lead or Medical Director for clinical development programs. This role ensures patient...position supports the design, execution, and data interpretation of global clinical trials. **Key Responsibilities** **Core Clinical Development Duties:**… more
- AbbVie (Mettawa, IL)
- …industry consortiums, key opinion leaders, research organizations, patient advocacy groups). The Associate Director represents HEOR at global regulatory and ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Patient Centered Outcomes Research, is responsible for… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The ** Associate Director , Development Strategy Analyst** is an experienced clinical ... research professional skilled in analyzing clinical trial data. They use this expertise to assess study feasibility, select countries and sites, and create… more
- Lilly (Indianapolis, IN)
- …and guidance to speed the delivery of medicines to patients globally. The Associate Director - Clinical Results Reporting Systems role requires broad expertise ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...Tech@Lilly, and other components of the R&D organization, the Associate Director - Results Reporting Systems is… more
- Astellas Pharma (Northbrook, IL)
- …patient segmentation, and biomarker identification + Conducts bioinformatics analysis of clinical trial omics data to support POM and patient selection + Supports ... data ingestion and conducts analysis using translational and biomarker data management platforms + Selects the appropriate data sets and analytical approaches for drug target identification and validation to support drug research + Develops new analysis tools… more
- System One (King Of Prussia, PA)
- …meets industry and regulatory requirements for clinical trial coding. The Associate Medical Coding Director manages and oversees staff, strategic partners, ... Title: Associate Medical Coding Director Full Time...to maximize effectiveness and maintain budgets. + Leads clinical trial coding deliverables and activities that support regulatory commitments… more
- Takeda Pharmaceuticals (Boston, MA)
- …and the development of scientific communications strategy and deliverables, the ** Associate Director , Scientific Communications Lead, Solid Tumors** proactively ... empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to...in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and… more
- Bristol Myers Squibb (Princeton, NJ)
- …development and implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative ... work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , Statistical Programming, provides functional expertise and… more
- Pfizer (Pearl River, NY)
- **Role Summary** The Global Clinical Lead functions independently and has direct experience with all the steps in designing and delivering results of clinical ... applying extensive expertise and in-depth knowledge of clinical research to lead global clinical research programs and registration activities across one or more… more
- Bristol Myers Squibb (Princeton, NJ)
- …by leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... a centralized triage function for informed consent negotiations with global clinical trial sites, IRBs/ECs, and health... Director of Informed Consent Management. The AD will be… more
- ADM (Kennesaw, GA)
- **92116BR** **Job Title:** Associate Director , Microbiome Regulatory Science - Kennesaw, GA **Department/Function:** Legal, Compliance, Regulatory Affairs, ... Corporate Security **Job Description:** ** Associate Director Microbiome - Decatur, IL; Chicago,...trial strategy for is aligned with the RSA global microbiome strategy. In addition, review and provide feedback… more
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