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Global Head of Pharmacology

Boston, MA, United States

About the Job:

TGI Life Sciences is collaborating with a global CRO company who is seeking a dynamic and experineced Global Head of Pharmacology to lead the international teams. This company is a listed international CRO with the operation based in Boston, the US.

This key position entails managing all pharmacology operations, spearheading strategic initiatives, and ensuring that preclinical activities are aligned with our corporate goals.

Job Responsibilities:

• Lead and supervise the preclinical pharmacology teams situated in Boston and China, fostering seamless collaboration and exceptional performance across both locations.

• Formulate and execute global strategies for preclinical research, harmonizing them with the company’s objectives and regulatory standards.

• Direct the planning, implementation, and evaluation of pharmacology studies, guaranteeing efficiency, adherence to regulatory norms, and fulfillment of client requirements.

• Act as a primary liaison between the company and clients, ensuring transparent communication of project advancements and resolution of any arising issues.

• Cultivate an environment of creativity within the team by integrating cutting-edge technologies and methodologies into preclinical research.

• Effectively manage finances, resources, and schedules across various projects, ensuring optimal allocation and utilization.

• Facilitate the professional advancement of team members through mentorship, training, and performance assessments.

• Regularly travel between Boston and China to oversee operations and maintain seamless team integration.

Qualification:

• Preferred: Doctorate (PhD) in Immunology, Pharmacology, Toxicology, or a related discipline.

•10 years + of experience in preclinical pharmacology within either a CRO or the pharmaceutical sector, including a minimum of 5 years in a managerial capacity.

• Demonstrated success in leading global teams and overseeing interdisciplinary initiatives.

• Profound comprehension of the drug development continuum, encompassing regulatory prerequisites and industrial benchmarks.

• On-site in Boston.

• Fluent in Chinese.

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