- Amgen (Washington, DC)
- …experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company). + Experience at, or oversight of, ... team, you will support programs and study teams, collaborate with senior management , and partner with internal stakeholders and suppliers for process improvement. We… more
- Amgen (Washington, DC)
- …development experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company) + Experience in development lifecycle management to include ... in-licensing and out-licensing activities and partner relationships Support product lifecycle management for new indications as directed by Global Development Lead +… more
- Charles River Laboratories (Ashland, OH)
- …of assigned nonclinical research studies of basic complexity, to include study management , interpretation, and reporting of study data, and assuring the regulatory ... with minimal oversight. * Develop critical thinking, troubleshooting, and time management skills aligned with needs of operational areas. * Demonstrate effective… more
- US Tech Solutions (IL)
- …* Minimum of 3-6 years of HEOR experience with proven high performance in the pharmaceutical industry, CRO , academia, or consulting. * Success in two or more ... that enhance our product's value proposition. The role demands strong project management , time management , and interpersonal skills to lead cross-functional… more
- LGC Group (Milford, MA)
- …the extended life sciences industry. We partner with IVD assay developers, pharmaceutical , CRO and academic institutions in commercialization activities across ... with on a regular basis are manufacturing, disease state procurement, and materials management . To perform this job successfully, an individual must be able to… more
- Amgen (Washington, DC)
- …clinical research experience obtained working on clinical trials at a biotech, pharmaceutical , or CRO company + Patient recruitment, retention and DCT ... trial (DCT) strategies in partnership with clinical program team, global study management and cross-functional data teams to deliver a fully optimized action plan.… more
- Charles River Laboratories (Shrewsbury, MA)
- …research studies at all levels of complexity. Responsibilities include study management , interpretation, and reporting of study data and assuring the regulatory ... and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting. * Provide prompt verbal… more
- Lilly (San Diego, CA)
- …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 ... to those who need them, improve the understanding and management of disease, and give back to our communities...+ At least 6 or more years of relevant pharmaceutical , biotech industry, or drug development experience, supporting clinical… more
- Astellas Pharma (Northbrook, IL)
- …of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We ... MS) of experience in applying statistical methods in biomedical research, Pharma, CRO , Academia or Healthcare industry or in providing statistical direction in these… more
- Kelly Services (South San Francisco, CA)
- …in drug substance process development, technology transfer, and external partnership management across our investigational and commercial portfolio. Reporting to the ... scientific data for global regulatory submissions. + External Partnership Management : Oversee productive collaborations with Contract Development and Manufacturing… more