Biotalent is collaborating with a consumer healthcare company who are looking for an expert in clinical pharmacology (phase I) to take the lead on clinical research activities with a focus on clinical pharmacology phase I PK and bioequivalence trials.

This is a stand alone, SME position (no line management) and expectations to be on site 2-3 times a week.

Role Responsibilities:

• Provide clinical pharmacology expertise, including biowaiver assessments and clinical development planning.
• Review clinical study protocols and key documents.
• Supervise study setup and execution, including risk management and protocol deviations.
• Collaborate with Biostatisticians for clinical trial data review.
• Ensure high-quality standards meet scientific and regulatory requirements.

Qualifications:

• Bachelor’s Degree in Life Science, Clinical Pharmacology, or Pharmacokinetics.
• Strong experience in pharmacokinetics within a CRO or pharmaceutical environment.
• Experience in phase I clinical trials.