- Merck & Co. (Durham, NC)
- …activities for pipeline vaccine programs.- This is position will support vaccine drug substance site readiness and technology transfer focusing on either upstream, ... and implementation of processes, systems and facilities related to vaccine drug substance and key intermediates eg buffers, media and cleaning solutions.Actively… more
- Genmab (NJ)
- …Role The Senior Oncology Account Manager builds and maintains strong professional relationships with key customers and stakeholders in private practice, medical ... challenging customers with value-based solutionsRepresent Genmab's brands in a professional , compliant, ethical, and effective mannerDemonstrates thorough understanding of… more
- MCKESSON (Cary, NC)
- …bonus. Key Responsibilities: Counsel and educate new/existing patients on specialty drug therapies. Adherence to contracted and accrediting regulations as indicated ... by drug specification. Complete, thorough, and accurate documentation utilizing good...preferably Ability to read, analyze and interpret practice standards, professional journals, technical procedures and government standards and regulations… more
- Merck & Co. (Rahway, NJ)
- …statistical programming activities for multiple and/or late stage drug /vaccine clinical development projects. -Accountability predominantly includes the development ... include coordinating the activities of a programming team.US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level… more
- Merck & Co. (North Wales, PA)
- …This position supports statistical programming activities for late stage drug /vaccine clinical development projects. This may include leadership of one ... processes (SOPs) and software development life-cycle (SDLC)US and/or worldwide drug or vaccine regulatory application submission experience including the development… more
- Eisai, Inc (Philadelphia, PA)
- …including but not limited to Emerging MarketsAdvance experience with the drug development process and eCTD regulatory submission standardsExpert understanding of ... experience creating timelines for the development and submission of drug filings to regulatory health authoritiesExcellent organizational skills to support… more
- Insmed Incorporated (NJ)
- …development and application of AI/ML models to accelerate discovery in areas like drug development, genomics, and rare disease research. This position is ideal for ... both computational and biological questions.Interest or experience in rare diseases, drug repurposing, or AI-driven biomedical discovery. Where You'll Work This is… more
- Merck & Co. (Orange County, CA)
- …in a complex buying environment, including multiple channels of drug distribution (Oncology group purchasing organizations, wholesalers, and specialty pharmacies). ... least 8 years of equivalent experience. Equivalent experience can be professional sales experience, work experience in the healthcare/scientific field with oncology… more
- Cipla (Fall River, MA)
- Job Title : QA Analyst I (AQA) FLSA Classification : Professional , Exempt Work Location : Fall River, MA Work Hours: General: 8:30 AM - 5:00 PM (may vary based on ... activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices… more
- BioAgilytix (San Diego, CA)
- …fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety ... record in a Commercial environmentAbility to build relationships through professional sales and interpersonal skills with a disciplined and...effectively with a wide variety of people in a professional manner, face to face, on the telephone and… more
