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- Tasks: Lead clinical pharmacology support and manage clinical trials from phase 1 to phase 2.
- Company: Join a leading Biopharmaceutical organization making a real impact in healthcare.
- Benefits: Work remotely from the UK, Netherlands, or Switzerland with flexible options.
- Why this job: Be part of a dynamic team, influence clinical development, and enhance your expertise in pharmacology.
- Qualifications: PhD in a relevant field with experience in clinical pharmacology and data interpretation required.
- Other info: Collaborate with colleagues in the US in a highly matrixed environment.
The predicted salary is between 43200 - 72000 £ per year.
Biotalent are seeking an experienced Associate Director in Clinical Pharmacology to join a leading Biopharmaceutical organisation. The ideal candidate will have a strong background in clinical pharmacology, pharmacokinetics (PK), and pharmacodynamics (PD), with the ability to critically evaluate and interpret data and manage clinical trials (phase 1 to phase 2). This role requires excellent communication skills and the ability to work independently in a highly matrixed environment with main collaboration with colleagues in the US. This role can be based in the UK, Netherlands or Switzerland. Key Responsibilities : Provide clinical pharmacology support independently and guidance to clinical stage project teams. Lead the analysis, interpretation, integration, and reporting of clinical pharmacology data. Conduct PK and PK/PD analysis to guide clinical development decisions. Prepare and contribute to regulatory submissions, including INDs, CTAs, and NDAs. Qualifications : A PhD in a relevant field with significant experience in the pharmaceutical/biotech industry. In-depth knowledge of clinical pharmacology, PK/PD , and clinical data interpretation. Proficiency in using pharmacokinetic modelling and data visualisation tools such as Phoenix WinNonlin, R, or NONMEM.
Associate Director - Clinical Pharmacology employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director - Clinical Pharmacology
✨Tip Number 1
Make sure to highlight your experience in clinical pharmacology and your proficiency with PK/PD analysis during networking events or informational interviews. This will help you stand out to potential employers who are looking for specific expertise.
✨Tip Number 2
Engage with professionals in the biopharmaceutical industry through LinkedIn or relevant forums. Sharing insights or asking questions about clinical trials can showcase your knowledge and passion, making connections that could lead to job opportunities.
✨Tip Number 3
Consider attending industry conferences or workshops focused on clinical pharmacology. These events not only provide valuable learning experiences but also allow you to meet key players in the field who might be hiring.
✨Tip Number 4
Stay updated on the latest trends and advancements in clinical pharmacology and pharmacokinetics. Being knowledgeable about current research and regulatory changes can give you an edge in discussions with potential employers.
We think you need these skills to ace Associate Director - Clinical Pharmacology
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly understand the responsibilities and qualifications required for the Associate Director in Clinical Pharmacology position. Highlight your relevant experience in clinical pharmacology, PK, and PD in your application.
Tailor Your CV: Customize your CV to emphasize your background in clinical pharmacology and any experience with managing clinical trials. Include specific examples of your work with PK/PD analysis and regulatory submissions.
Craft a Compelling Cover Letter: Write a cover letter that showcases your communication skills and ability to work independently in a matrixed environment. Mention your proficiency with pharmacokinetic modeling tools and how they relate to the role.
Highlight Collaboration Experience: Since the role involves collaboration with colleagues in the US, be sure to mention any previous experience working in international teams or cross-functional projects. This will demonstrate your ability to thrive in a collaborative setting.
How to prepare for a job interview at BioTalent
✨Showcase Your Expertise
Be prepared to discuss your background in clinical pharmacology, pharmacokinetics, and pharmacodynamics in detail. Highlight specific projects or trials you've worked on, especially those that involved critical data evaluation and interpretation.
✨Demonstrate Communication Skills
Since this role requires excellent communication skills, practice articulating complex concepts clearly and concisely. Be ready to explain how you would collaborate with teams, particularly with colleagues in the US.
✨Familiarize Yourself with Regulatory Submissions
Understand the process of preparing regulatory submissions like INDs, CTAs, and NDAs. Be ready to discuss your experience with these documents and how you can contribute to successful submissions.
✨Prepare for Technical Questions
Expect technical questions related to PK/PD analysis and pharmacokinetic modeling tools. Brush up on your knowledge of tools like Phoenix WinNonlin, R, or NONMEM, and be prepared to discuss how you've used them in past projects.
