Senior Principal Scientist, Nonclinical Drug Safety

At Merck & Co., we are committed to developing innovative and life-changing medicines that make a difference in people's lives. As a global leader in the pharmaceutical industry, we are seeking a highly experienced Senior Principal Scientist to join our Nonclinical Drug Safety team. As a key member of our research and development team, you will play a critical role in ensuring the safety and efficacy of our drug candidates. We are looking for a dedicated and driven individual with a strong background in nonclinical drug safety and a passion for making a positive impact on human health. If you are ready for a challenging and rewarding career with a company that values your expertise and contributions, then we encourage you to apply for this exciting opportunity.

1. Conduct in-depth research and analysis to assess the safety and efficacy of potential drug candidates.
2. Develop and implement nonclinical safety strategies to support the development of new medicines.
3. Lead and manage preclinical studies, including study design, protocol development, and data analysis.
4. Provide expert guidance and recommendations to cross-functional teams on nonclinical safety issues.
5. Collaborate with internal and external stakeholders, including regulatory agencies, to ensure compliance with safety standards and regulations.
6. Continuously evaluate and improve nonclinical safety processes and procedures.
7. Stay current with industry developments and trends related to nonclinical drug safety.
8. Mentor and train junior scientists on nonclinical safety principles and methodologies.
9. Participate in the preparation and submission of regulatory documents, including Investigational New Drug (IND) applications.
10. Represent the company at scientific conferences and meetings to share research findings and promote the company's expertise in nonclinical drug safety.
11. Communicate safety information and risk assessments to stakeholders, including senior management and external partners.
12. Collaborate with other departments, such as toxicology, pharmacokinetics, and clinical development, to ensure a comprehensive understanding of drug safety profiles.
13. Comply with all relevant company policies and procedures, as well as regulatory requirements.
14. Maintain accurate and up-to-date records of all research activities.
15. Serve as a subject matter expert on nonclinical safety issues and provide guidance on regulatory submissions and interactions.

According to JobzMall, the average salary range for a Senior Principal Scientist, Nonclinical Drug Safety in Rahway, NJ 07065, USA is $150,000-$200,000 per year. However, this can vary depending on the specific company, industry, and individual qualifications and experience. It is best to research the specific company and job listing for a more accurate salary range.

Merck & Co., Inc., d.b.a. Merck Sharp & Dohme outside the United States and Canada, is an American multinational pharmaceutical company and one of the largest pharmaceutical companies in the world. Merck & Co., Inc. engages in the provision of health solutions through its prescription medicines, vaccines, biologic therapies, animal health, and consumer care products. It operates through the following segments: Pharmaceutical, Animal Health, Alliances and Healthcare Services. The Pharmaceutical segment includes human health pharmaceutical and vaccine products marketed either directly by the company or through joint ventures.