At a Glance
- Tasks: Lead innovative pharmacometric analyses and guide teams in drug development.
- Company: Dynamic company at the forefront of clinical pharmacology and drug strategy.
- Benefits: Comprehensive benefits, competitive salaries, flexible working hours, and professional development opportunities.
- Other info: Opportunities for remote work, leadership roles, and career progression.
- Why this job: Make a meaningful impact in drug development while collaborating with experts in the field.
- Qualifications: 6-10 years in drug development, regulatory experience, and proficiency in relevant software.
The predicted salary is between 70000 - 90000 £ per year.
Step into a role where science meets strategy and your expertise shapes the future of drug development. As an Associate Director/Director, Pharmacometrician, you'll lead high-impact modeling and simulation efforts within a dynamic Clinical Pharmacology, Modeling and Simulation (CPMS) environment. You'll guide teams, mentor pharmacometricians, and provide strategic insight to clients at key development milestones. This role also offers the opportunity to represent clients in interactions with regulatory agencies. If you thrive on collaboration and solving complex scientific challenges, this is your chance to make a meaningful impact.
About the role
This role combines scientific leadership and strategic impact, leading population PK analyses while developing innovative approaches to improve efficiency and accuracy. You will design, analyze, and interpret clinical pharmacology studies, provide strategic guidance to clients, and contribute to regulatory documents and agency interactions. In addition, you'll foster client relationships, support business development, and stay at the forefront of PK/PD advancements to drive continuous improvement.
Responsibilities
- Lead and conduct population PK analyses using advanced modeling tools and methodologies
- Develop and implement innovative approaches to enhance the efficiency and accuracy of PK analysis
- Design, analyze, and interpret clinical pharmacology studies (renal, hepatic, TQT, ADME, DDI, BE/BA, SAD, MAD, etc.) and provide guidance to optimize pharmacokinetic sampling and dosing strategies
- Provide strategic guidance to clients, owning deliverables and developing clinical pharmacology plans
- Author and review PK reports and clinical pharmacology sections of regulatory documents
- Represent clients in regulatory interactions and contribute to business development and relationship management
Requirements
- Life science, healthcare and/or business degree
- Minimum 6-10 years of relevant work experience, including experience in drug development, clinical pharmacology, and pharmacometrics
- Regulatory experience including regulatory report writing essential
- Experience with regulatory submissions including INDs, CTAs, regulatory meetings and NDA/BLA/MAA submissions
- Proficiency in NONMEM, Pirana, and R software preferred
- Excellent organizational, negotiating and financial skills
Benefits
- 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
Associate Director, Pharmacometrics in Bracknell employer: Allucent
Allucent is an exceptional employer that prioritises employee well-being and professional growth, offering a flexible remote or hybrid working environment tailored to the needs of our team. With a strong commitment to compliance and data quality in clinical programming, we provide comprehensive benefits and opportunities for career advancement, making it a rewarding place for those passionate about drug development.
