Senior Principal Scientist, Nonclinical Drug Safety

"Are you a highly motivated and experienced scientist looking for a new challenge? Do you have a passion for drug safety and a desire to make a difference in patients' lives? If so, we have an exciting opportunity for you at Merck & Co. as a Senior Principal Scientist in Nonclinical Drug Safety. Our company is dedicated to improving human health through innovative medicines and we are seeking an exceptional individual to join our team. In this role, you will lead and oversee nonclinical safety assessment for our drug development programs, providing scientific expertise and guidance to ensure the safety and efficacy of our products. To excel in this position, you must have a PhD in a relevant scientific field, at least 10 years of experience in nonclinical drug safety, and a strong understanding of regulatory guidelines and requirements. Join us in our mission to create a healthier world and be a part of a dynamic and collaborative team of scientists at Merck & Co."

1. Lead and oversee the nonclinical safety assessment for drug development programs.
2. Provide scientific expertise and guidance to ensure the safety and efficacy of products.
3. Collaborate with cross-functional teams to design and implement nonclinical safety studies.
4. Analyze and interpret data from nonclinical studies and communicate findings to stakeholders.
5. Develop and implement safety strategies for new drug candidates.
6. Stay current with regulatory guidelines and requirements related to nonclinical drug safety.
7. Manage and mentor a team of scientists and research associates.
8. Serve as the primary point of contact for nonclinical safety questions and concerns.
9. Contribute to the development and review of safety sections in regulatory submissions.
10. Participate in internal and external meetings, presenting nonclinical safety data and recommendations.
11. Identify and mitigate potential safety issues during drug development.
12. Collaborate with external partners and vendors to conduct nonclinical safety studies.
13. Contribute to the development and implementation of nonclinical safety policies and procedures.
14. Assist in budget planning and resource allocation for nonclinical drug safety projects.
15. Continuously evaluate and improve nonclinical safety processes and procedures.
16. Represent the company at scientific conferences and meetings related to drug safety.
17. Maintain a high level of scientific rigor and adhere to ethical standards in all work.
18. Act as a subject matter expert on nonclinical drug safety for regulatory agencies, as needed.
19. Mentor and train junior scientists on nonclinical safety principles and best practices.
20. Collaborate with other departments, such as clinical safety and pharmacovigilance, to ensure alignment and consistency in safety assessments.

According to JobzMall, the average salary range for a Senior Principal Scientist, Nonclinical Drug Safety in Boston, MA, USA is $149,000 - $194,000 per year. This may vary depending on the specific company, experience level, and other factors.

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.