Clinical Pharmacology Lead

1 month ago


Weybridge, Surrey, United Kingdom Haleon Full time
About the Role

The Associate Director, Clinical Pharmacology is a key position within our organization, responsible for leading clinical research activities with a focus on clinical pharmacology phase I pharmacokinetics and bioequivalence trials.

Key Responsibilities
  • Provide clinical pharmacology expertise, including biowaiver assessments, to support the development of our products.
  • Develop and review clinical study protocols to ensure they meet the highest standards of scientific and regulatory excellence.
  • Contribute to the preparation of key study documents, including the Investigator's Brochure and clinical study reports.
  • Supervise the setup and execution of clinical trials, ensuring that they are conducted in accordance with regulatory requirements and industry best practices.
  • Collaborate with biostatisticians to analyze and interpret clinical trial data.
Requirements

To be successful in this role, you will need:

  • A Bachelor's Degree in Life Science, Clinical Pharmacology, or a related field.
  • A minimum of 8 years of experience in pharmacokinetics, preferably in the pharmaceutical industry or a CRO.
  • Excellent communication and interpersonal skills, with the ability to work effectively in a multi-functional team.
  • Strong analytical and problem-solving skills, with the ability to handle complex issues with initiative and integrity.
Preferred Qualifications

We are looking for candidates with advanced scientific degrees, such as a PhD, and experience in bioanalytical science. Fluency in English is required, and bi-lingual skills in French are a plus.

We are committed to creating an inclusive and diverse work environment, where everyone feels valued and empowered to contribute their best work. If you are passionate about clinical pharmacology and want to be part of a dynamic team, we encourage you to apply.



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