Associate Director, Clinical Pharmacology
Associate Director, Clinical Pharmacology

Associate Director, Clinical Pharmacology

Glasgow Full-Time 72000 - 108000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead clinical pharmacology projects and guide teams in innovative drug development.
  • Company: Global biotech organisation focused on CNS disorders with a collaborative culture.
  • Benefits: Competitive salary, dynamic work environment, and opportunities for professional growth.
  • Why this job: Make a real impact in cutting-edge clinical development for life-changing therapeutics.
  • Qualifications: PhD in clinical pharmacology and extensive industry experience required.
  • Other info: Join a rapidly growing team with excellent career advancement opportunities.

The predicted salary is between 72000 - 108000 £ per year.

RBW are partnered with a global biotech organisation that are seeking an experienced and driven Associate Director in Clinical Pharmacology to support a rapidly growing portfolio of therapeutics targeting central nervous system disorders. This role offers a unique opportunity to contribute to cutting-edge clinical development in a dynamic and collaborative environment.

Responsibilities:

  • Serve as the clinical pharmacology lead providing scientific and strategic guidance to project teams
  • Provide guidance for dosing regimen and informing best strategy for modelling techniques
  • Perform PK and PK/PD analyses to support clinical trial design and execution
  • Contribute to regulatory submissions, including briefing documents, INDs, CTAs, and NDAs
  • Overseeing development of junior clinical pharmacology scientists
  • Support scientific publications through the preparation of abstracts and manuscript

Requirements:

  • PhD in clinical pharmacology, pharmacokinetics or a relevant field
  • Extensive experience in the pharmaceutical or biotech industry, with a strong background in clinical pharmacology and PK/PD modeling
  • Previous hands on Population PK/PD modelling and simulation experience is desirable
  • Strong knowledge of clinical pharmacology guidelines for regulatory submissions
  • Proficient user of NONMEM, Phoenix WinNonlin, R etc

Associate Director, Clinical Pharmacology employer: RBW Consulting

Join a pioneering global biotech organisation that champions innovation and collaboration in the field of clinical pharmacology. With a strong commitment to employee development, you will have access to extensive growth opportunities and a supportive work culture that values your contributions to advancing therapeutics for central nervous system disorders. Located in a vibrant area, this role not only offers a chance to work on groundbreaking projects but also provides a unique environment where your expertise can truly make a difference.
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Contact Detail:

RBW Consulting Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Associate Director, Clinical Pharmacology

✨Tip Number 1

Network like a pro! Reach out to your connections in the biotech and pharmaceutical fields. Attend industry events or webinars where you can meet potential employers and showcase your expertise in clinical pharmacology.

✨Tip Number 2

Prepare for interviews by brushing up on your PK/PD modelling knowledge. Be ready to discuss your hands-on experience with tools like NONMEM and Phoenix WinNonlin, as well as how you've contributed to regulatory submissions in the past.

✨Tip Number 3

Showcase your scientific publications! If you've prepared abstracts or manuscripts, make sure to highlight these during interviews. It demonstrates your ability to contribute to the scientific community and adds credibility to your profile.

✨Tip Number 4

Don't forget to apply through our website! We have a range of opportunities that might just be the perfect fit for you. Plus, it shows you're proactive and genuinely interested in joining our team.

We think you need these skills to ace Associate Director, Clinical Pharmacology

Clinical Pharmacology
Pharmacokinetics
PK/PD Modelling
Population PK/PD Modelling
Regulatory Submissions
NONMEM
Phoenix WinNonlin
R
Scientific Publication Preparation
Project Leadership
Strategic Guidance
Dosing Regimen Development
Analytical Skills
Collaboration Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Associate Director role. Highlight your experience in clinical pharmacology and any relevant projects you've led. We want to see how your background aligns with our needs!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical pharmacology and how you can contribute to our team. Keep it engaging and personal – we love to see your personality!

Showcase Your Skills: Don’t forget to showcase your technical skills, especially in PK/PD modelling and simulation. Mention specific tools like NONMEM or R that you’re proficient in. We’re looking for someone who can hit the ground running!

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any updates from us!

How to prepare for a job interview at RBW Consulting

✨Know Your Stuff

Make sure you brush up on your clinical pharmacology knowledge, especially around PK/PD modelling. Be ready to discuss your previous experiences and how they relate to the role. This is your chance to show off your expertise!

✨Prepare for Technical Questions

Expect some in-depth questions about dosing regimens and modelling techniques. Practise explaining your thought process clearly and concisely. It’s all about demonstrating your analytical skills and strategic thinking.

✨Show Your Collaborative Spirit

This role is all about teamwork, so be prepared to talk about how you've worked with project teams in the past. Share examples of how you’ve contributed to a collaborative environment and supported junior scientists.

✨Familiarise Yourself with Regulatory Submissions

Since you'll be contributing to regulatory submissions, make sure you understand the key documents like INDs and NDAs. Being able to discuss your experience with these will show that you’re ready to hit the ground running.

Associate Director, Clinical Pharmacology
RBW Consulting

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