- Merck & Co. (San Diego, CA)
- …Management Process, Medical Research, Mentorship, Parasitology, Patient Care, Professional Networking, Protocol Development, Regulatory Compliance ... and clinical research methodology and biostatistics principles.Prior experience in drafting regulatory documents and interactions with global regulatory agencies… more
- Merck & Co. (San Francisco, CA)
- …tumor size and survival. A Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring ... regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications (CTDs), and representing QP2-IO at regulatory … more
- Merck & Co. (South San Francisco, CA)
- …Within QP2, you have a uniq ue oppor t unity to accelerate your professional career as a quantitative drug developer taking advantage of our end-to-end pipeline ... external vendors and partners, creating an aligned, quantitative and model-informed regulatory framework to impact strategies and decisions of drug discovery and… more
- Aequor (Thousand Oaks, CA)
- …of DP technical process, manufacturing operations, scientific method, basic regulatory compliance expectations, and quantitative / analytical troubleshooting ... Standard business hours You've worked hard to become the professional you are today and are now ready to...leadership team. Additional Responsibilities include: Engaging with Quality and Regulatory teams to ensure alignment and compliance … more
- Merck & Co. (San Francisco, CA)
- …proportional hazards models. Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring ... regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs),...Proficiency in R, NONMEM or other similar programing language. Professional working proficiency in written and verbal communication. #EligibleforERP#QP2Current… more
- Eisai, Inc (San Jose, CA)
- …approved promotional clinical trials, patient access to medication, and regulatory / compliance guidelines preferred.Experience with account planning and ... to relevant customer stakeholders in a compliant way.Monitor operating costs and compliance with territory budget.Seek out mentorship to learn and build key sales… more
- Lundbeck (Fresno, CA)
- …issues (IDNs, Medicare, Medicaid, Commercial) using Lundbeck resources. Pharmaceutical Environment/ Compliance - Apply knowledge of pharmaceutical and regulatory ... and Porterville. SUMMARY: Are you a results-driven biopharmaceutical sales professional looking to be part of an organization that...growth! We are seeking a dynamic and results-driven sales professional with a proven track record of success who… more
- Lundbeck (Oakland, CA)
- …Livermore, Fremont & Milpitas. SUMMARY: Are you a results-driven biopharmaceutical sales professional looking to be part of an organization that values being ... issues (IDNs, Medicare, Medicaid, Commercial) using Lundbeck resources. Pharmaceutical Environment/ Compliance - Ability to apply knowledge of pharmaceutical and … more
- Merck & Co. (South San Francisco, CA)
- …Within QP2, you have a uniq ue oppor t unity to accelerate your professional career as a quantitative drug developer taking advantage of our end-to-end pipeline ... independence in a similar role in pharmaceutical drug development, regulatory agency, or academia. Educational background in biopharmaceutics, pharmaceutical… more
- Stantec (Sacramento, CA)
- …processes and requirements, decision-making frameworks, and/or NEPA/CEQA or other regulatory compliance processes. + Professional certification/registration ... with project managers, project engineers and scientists, clients, communities, regulatory agencies, and subcontractors. Contribute to the development of our… more
