- Takeda Pharmaceuticals (Boston, MA)
- …the role oversees external programs at CROs, including the design and management of diverse types of assays, execution, and acceleration of the iterative ... series in depth to provide scientific insights. + Proactively leverage external CRO capabilities by integrating both internal and external expertise to establish an… more
- Charles River Laboratories (Rockville, MD)
- …and corrective actions, and line clearances. + Develop and execute training and Management briefings at any technical or compliance level required on updates and ... ensure necessary Quality oversight to areas within span of control . + Effectively model, demonstrate and live an employee-focused...+ Minimum 8 years of experience in a biologics, pharmaceutical , medical device, or related industry. 10 years of… more
- Charles River Laboratories (Reno, NV)
- …or related field preferred. + At least ten years experience in scientific and management in the life sciences, pharmaceutical , or contract research fields. + ... Knowledge of business and operations management and a good understanding of pharmaceutical ,...River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory… more
- GRAIL (Menlo Park, CA)
- …Provides oversight of regional study monitors and/or contract research organizations ( CRO )Facilitate external communication with site staff and pharmaceutical ... United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com… more
- Amgen (Washington, DC)
- …drug development and commercialization process + Operations experience within a biotech, pharmaceutical or CRO company + Toolsets/skills required to drive ... information technologies/information systems, analytics platforms and reporting technology and pharmaceutical industry + Previous oversight of information system vendors… more
- Lilly (Indianapolis, IN)
- …bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and ... involved in key activities for the development of synthetic active pharmaceutical ingredients from pre-clinical phases through commercialization of drug substances… more
- Lilly (Indianapolis, IN)
- …bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and ... involved in key activities for the development of synthetic active pharmaceutical ingredients (API) from pre-clinical phases through commercialization of drug… more
- Charles River Laboratories (Memphis, TN)
- …validation. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Responsible for personnel management activities such as: scheduling, personnel actions * (hiring, promotions, ... years of experience in computer system validation within a regulated industry ( pharmaceutical , medical device, biotechnology). * Minimum of 5 years of experience… more
- Pfizer (Groton, CT)
- …of related experience in a Clinical Pathology laboratory, hospital clinical laboratory, pharmaceutical company, CRO , or diagnostic company + American Society of ... novel platform development data in support of the safety assessment of pharmaceutical drug candidates in compliance with GLP regulatory standards as applicable… more
- Takeda Pharmaceuticals (Boston, MA)
- …Support global communications, including coordination of information between TBOS and TSHO + ** CRO Management Support for In Vitro Pharmacology** + Ensure IVP ... Director in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more