Merck
Pharma · Pharma
- HQ
- Rahway, US
- Founded
- 1891
- Size
- 70,000+
- Website
- merck.com
Currently tracking 14 active AI roles, up 295% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $129k–$203k (avg $166k).
| Title | Stage | AI score |
|---|---|---|
| R&D Clinical Research General and Specialty Medicine, Associate Principle Scientist (M.D.) Associate Principal Scientist role in R&D Clinical Research for General and Specialty Medicine at Merck, focusing on oncology-adjacent areas like General Medicine, Infectious Diseases, and Vaccines. Responsibilities include providing medical expertise to development teams, reviewing documents, leading clinical development plans in Japan in collaboration with US headquarters, engaging with scientific leaders, and supporting academic presentations/publications. Requires an MD with 5+ years of clinical experience in cardiology or equivalent, strong collaboration, English negotiation/speaking/writing skills, and fluent Japanese. | — | 0 |
| Medical Affairs Oncology Medical Advisor (M.D.) This role at Merck focuses on medical affairs within oncology, involving the design, planning, and execution of medical research, development of country medical affairs plans, and engagement with scientific leaders. It requires clinical and research experience in healthcare, knowledge of pharmaceutical regulations, and experience with scientific publications or presentations. The role emphasizes strategic thinking, scientific communication, and fostering collaboration within a global context. |
| — |
| 0 |
| R&D Oncology Clinical Science Clinical Research Sr. Scientist This role at Merck focuses on clinical research in oncology, involving the planning, execution, and reporting of clinical trials. The scientist will collaborate with internal and external stakeholders, including regulatory bodies, to support the global development of new oncology drugs. Responsibilities include inputting into development strategy, preparing regulatory submission documents, managing clinical trial protocols, monitoring data, and contributing to publications. | — | 0 |
| R&D Regulatory Affairs Sr. Scientist（開発薬事） This role focuses on building and executing regulatory affairs strategies for new drug development in Japan, aligning with global strategies. It involves significant interaction with regulatory authorities like MHLW and PMDA, ensuring the quality of submission documents, and coordinating the preparation and submission of applications. The position requires a background in life sciences, experience in pharmaceutical development and regulatory submissions, and strong English communication skills for international coordination. | — | 0 |
| Outcomes Research This role focuses on developing and executing Health Economics and Outcomes Research (HEOR) strategies for pharmaceutical assets, generating evidence to support market access, pricing, and reimbursement in Japan. Responsibilities include conducting economic analyses, developing value dossiers, managing literature reviews, performing database analyses, and coordinating cross-functional efforts. | — | 0 |