- Cytel (Raleigh, NC)
- …Good ad-hoc reporting skills. + Proficiency in Efficacy analysis. + Familiarity with drug development life cycle and experience with the manipulation, analysis ... and validating statistical programming deliverables (SDTM, ADAM, TFL's) in Early Development Statistics and PK/PD Modeling and Simulation spanning all therapeutic… more
- Norstella (Raleigh, NC)
- …must-have answers for critical strategic and commercial decision-making along the entire drug development journey. **The Role:** MMIT is seeking a Solution ... 05: Humility, Gratitude, and Learning **Benefits:** * Medical and Prescription Drug Benefits * Health Savings Accounts (HSA) or Flexible Spending Accounts… more
- IQVIA (Durham, NC)
- …management skills. Ability to work independently. + Comprehensive understanding of clinical drug development process. Ability to establish and maintain effective ... and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve… more
- IQVIA (Durham, NC)
- …Standards. * Understanding of regulated clinical trial environment and knowledge of drug development process. * Ability to establish and maintain effective ... and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve… more
- ICON Clinical Research (Raleigh, NC)
- …to clinical trials + Familiar with regulations and guidance governing clinical trials and drug development (eg ICH, FDA, GDPR, EMA covering GCP, GDP). + Audit ... on our mission to shape the future of clinical development . We are currently seeking a Principal Auditor Quality...for Imaging & Cardiac related external client relationships. + Development of the IMC annual internal audit schedule as… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …the critical clinical procedures on the different clinical studies + Interact with Drug Development department to provide guidance and consultancy to resolve ... than 110 countries and regions. **Primary Responsibilities:** + **Participate in the development and review of the Clinical SOPs, Regulatory documents and Study… more
- Two95 International Inc. (Durham, NC)
- …Rate: $Open/hr. Requirements General Responsibilities: + Plan and conduct analytical tests for drug development and transfer the methods to CDMO + Analyze and ... 10-12+ years of pharma industry analytical experience working within analytical development /validation to support solid oral dosage forms (small molecules), Ph.D.… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** **Director, QA Drug Substance Operations** Are you a strategic leader with expertise in managing teams of QA professionals and collaborating ... to lead and grow in a world-class Quality organization as the Director, QA Drug Substance Operations. In this role, you will oversee our Quality Product and… more
- Amgen (Holly Springs, NC)
- …while transforming your career. Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will ... The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The manufacturing associate in Drug Product Manufacturing will have a primary task for operation of filling line including all tasks related. ... + Contribute to the preparation for operational readiness related to bulk drug product manufacturing + Possible assignments include: Supporting projects related to… more