Director, Pharmacometrics in Luton

Director, Pharmacometrics in Luton

Luton Full-Time 36000 - 60000 £ / year (est.) No working from home possible
Allucent

At a Glance

  • Tasks: Lead drug development projects and guide teams in pharmacometric analyses.
  • Company: Join Allucent, a mission-driven company focused on innovative therapies.
  • Benefits: Enjoy competitive salaries, flexible working hours, and professional development opportunities.
  • Other info: Dynamic work environment with excellent career growth and leadership opportunities.
  • Why this job: Make a real impact in drug development while mentoring a talented team.
  • Qualifications: 8+ years in pharmacometrics with strong skills in NONMEM and R.

The predicted salary is between 36000 - 60000 £ per year.

Shape the future of drug development as our next Director of Pharmacometrics. You are not just a technical expert but a strategic thinker who loves solving tough development challenges through smart modeling. In this role, you will lead multiple projects, guide teams, and stay hands-on with PK and PK/PD analyses using tools like NONMEM and R. You will bring your regulatory know-how, storytelling skills, and passion for mentorship to help drive smarter, faster clinical decisions. If you are ready to make an impact and lead with both science and heart, we would love to meet you.

As Director of Pharmacometrics, you will lead from both the bench and the boardroom. You will oversee multiple projects, serving as the senior technical modeler and project lead through shaping strategy, guiding analysis, and driving decisions that move programs forward. You will collaborate closely with cross-functional teams to design, execute, and interpret population PK and PK/PD models that influence regulatory and clinical outcomes. Beyond the science, you will mentor a talented team of pharmacometricians, helping them grow technically and strategically while fostering a culture of curiosity and excellence.

Your main responsibilities will include but are not limited to:

  • Demonstrable hands-on experience of population PK, exposure-response, and PK/PD modeling in a clinical setting.
  • Solid understanding of the principles of model-informed drug development (MIDD) and its practical delivery.
  • Excellent technical and programming skills with population analysis and other software, including NONMEM and R as a minimum. Experience with Monolix and PKSim is a plus.
  • Collaborating in and leading matrix teams including junior modelers, programmers and other technical and project management staff.

About You

If you are curious, solution-driven and thrive in collaboration, blending deep technical skills in NONMEM and R with clear communication, regulatory know-how, and a passion for guiding teams to deliver smarter, faster drug development outcomes, you will thrive here. To be successful we are looking for the following traits and behaviours:

  • Higher degree in life science, medicine, biomathematics/engineering/statistics.
  • Minimum 8 years' experience as a pharmacometrician in clinical development.
  • Regulatory experience including regulatory report writing essential. Experience with regulatory submissions including INDs, CTAs, regulatory meetings and NDA/BLA/MAA submissions.

Benefits of working at Allucent include:

  • Comprehensive benefits package per location.
  • Competitive salaries per location.
  • Departmental Study/Training Budget for furthering professional development.
  • Flexible Working hours (within reason).
  • Opportunity for remote/hybrid working depending on location.
  • Leadership and mentoring opportunities.
  • Participation in our enriching Buddy Program as a new or existing employee.
  • Internal growth opportunities and career progression.
  • Financially rewarding internal employee referral program.
  • Access to online soft-skills and technical training via internal platforms.
  • Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects.
  • Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees.

If you are interested in this role please apply through the button or for more information reach out to Tiffany Wasti at Tiffany.wasti@allucent.com.

Director, Pharmacometrics in Luton employer: Allucent

At Allucent, we pride ourselves on being an exceptional employer that fosters a culture of collaboration, mentorship, and continuous growth. As the Director of Pharmacometrics, you will not only lead innovative drug development projects but also have access to comprehensive benefits, flexible working arrangements, and ample opportunities for professional development, all while working in a dynamic environment that values your contributions and encourages you to shine.

Allucent

Contact Details:

Allucent Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Director, Pharmacometrics in Luton

Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream role.

Tip Number 2

Prepare for interviews by practising common questions and scenarios related to pharmacometrics. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your storytelling skills. Remember, showcasing your passion and expertise can really set you apart!

Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the position. It’s a simple gesture that can leave a lasting impression on hiring managers.

Tip Number 4

Apply through our website! We love seeing candidates who are genuinely interested in joining us at Allucent. Plus, it gives you a chance to showcase your enthusiasm for our mission and values right from the start.

We think you need these skills to ace Director, Pharmacometrics in Luton

Population PK Modelling
PK/PD Modelling
NONMEM
R Programming
Model-Informed Drug Development (MIDD)
Regulatory Report Writing
IND Submissions

Some tips for your application 🫡

Show Your Passion:When writing your application, let your enthusiasm for drug development shine through. We want to see how your passion aligns with our mission to bring new therapies to light.

Be Specific About Your Experience:Make sure to highlight your hands-on experience with PK and PK/PD modelling. We love details, so mention the tools you've used like NONMEM and R, and any relevant projects you've led.

Tailor Your Application:Don’t just send a generic application! Tailor your CV and cover letter to reflect the specific skills and experiences that match the Director of Pharmacometrics role. We appreciate when candidates take the time to connect their background to our needs.

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!

How to prepare for a job interview at Allucent

Know Your Stuff

Make sure you brush up on your technical skills, especially in NONMEM and R. Be ready to discuss specific projects where you've applied population PK and PK/PD modelling. This will show that you're not just a theoretical expert but someone who can apply their knowledge practically.

Show Your Strategic Side

Prepare to talk about how you've shaped strategies in previous roles. Think of examples where your strategic thinking led to successful project outcomes. This is crucial for a Director role, so highlight your ability to lead from both the bench and the boardroom.

Mentorship Matters

Since mentoring is a key part of this role, be ready to share your experiences in guiding teams. Discuss how you've helped junior modelers grow and fostered a culture of curiosity and excellence. This will demonstrate your leadership style and commitment to team development.

Regulatory Know-How

Familiarise yourself with regulatory processes and be prepared to discuss your experience with submissions like INDs and NDAs. Highlight any specific instances where your regulatory knowledge made a difference in project outcomes, as this is essential for the role.