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- Tasks: Lead clinical pharmacology projects and analyze data to guide development strategies.
- Company: Join a dynamic biopharmaceutical company making waves in the industry.
- Benefits: Enjoy hybrid working options and a competitive salary package.
- Why this job: Be at the forefront of drug development and make a real impact in healthcare.
- Qualifications: PhD in Clinical Pharmacology or related field is a must.
- Other info: Reach out if you or someone you know is interested!
The predicted salary is between 54000 - 84000 £ per year.
Associate Director Pharmacology – Greater London area (hybrid working) – Competitive Package
BioTalent are delighted to be supporting a Biopharmaceutical company on their search for a permanent Associate Director of Pharmacology.
You will be responsible for:
- Serve as the Clinical Pharmacology lead, providing expert guidance and support to clinical-stage project teams.
- Lead the analysis, interpretation, integration, and reporting of clinical pharmacology data to inform development strategies.
- Conduct PK and PK/PD analyses to drive clinical decision-making.
- Contribute to regulatory submissions, including the preparation of briefing documents, INDs, CTAs, and NDAs.
You will bring the following:
- Must have a PHD in a relevant field (eg Clinical Pharmacology, Pharmacokinetics, Pharmacometrics).
- In depth knowledge of clinical pharmacology, pharmacokinetics, modeling and simulation, PK/PD principles, ADME and clinical data interpretation.
- In depth knowledge of international guidelines related to Clinical Pharmacology and Pharmacometrics.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email:
Mobile: 02038286064
I look forward to hearing from you!
Associate Director Pharmacology employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director Pharmacology
✨Tip Number 1
Make sure to highlight your experience in clinical pharmacology and any relevant projects you've led. This will show that you have the expertise needed for the role.
✨Tip Number 2
Network with professionals in the biopharmaceutical industry, especially those who have experience in pharmacokinetics and modeling. They can provide valuable insights and may even refer you to opportunities.
✨Tip Number 3
Stay updated on the latest international guidelines related to clinical pharmacology. Being knowledgeable about these can set you apart during discussions with potential employers.
✨Tip Number 4
Prepare to discuss specific examples of how you've contributed to regulatory submissions in the past. This will demonstrate your hands-on experience and understanding of the process.
We think you need these skills to ace Associate Director Pharmacology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD and relevant experience in clinical pharmacology, pharmacokinetics, and modeling. Use specific examples that demonstrate your expertise in PK/PD analyses and regulatory submissions.
Craft a Strong Cover Letter: Write a cover letter that clearly outlines your motivation for applying to this role. Emphasize your leadership experience in clinical-stage projects and your ability to provide expert guidance to teams.
Highlight Relevant Skills: In your application, focus on your in-depth knowledge of international guidelines related to Clinical Pharmacology and Pharmacometrics. Mention any specific software or methodologies you are proficient in that are relevant to the role.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no grammatical errors and that your documents are professionally formatted. A polished application reflects your attention to detail.
How to prepare for a job interview at BioTalent
✨Showcase Your Expertise
Make sure to highlight your PhD and any relevant experience in clinical pharmacology. Be prepared to discuss specific projects where you provided expert guidance and how your contributions impacted the outcomes.
✨Demonstrate Analytical Skills
Prepare to discuss your experience with PK and PK/PD analyses. Bring examples of how you've used these analyses to drive clinical decision-making, and be ready to explain your thought process during these evaluations.
✨Familiarize Yourself with Regulatory Guidelines
Since the role involves contributing to regulatory submissions, review international guidelines related to Clinical Pharmacology and Pharmacometrics. Be ready to discuss how you have applied these guidelines in past projects.
✨Engage with the Interviewers
Ask insightful questions about the company's current projects and future directions in pharmacology. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
