At a Glance
- Tasks: Lead clinical pharmacology support for innovative RNAi therapeutics and guide project teams.
- Company: Join Alnylam, a leader in RNAi innovation with a collaborative culture.
- Benefits: Work remotely with a focus on professional growth and impactful projects.
- Other info: Dynamic virtual role with excellent career advancement opportunities.
- Why this job: Make a difference in patients' lives through groundbreaking RNAi therapies.
- Qualifications: Ph.D. or Pharm.D. in relevant field with industry experience required.
The predicted salary is between 51750 - 63250 £ per year.
The Associate Director, Clinical Pharmacology supports a rapidly expanding clinical portfolio of RNAi therapeutics within the CNS franchise. This role provides clinical pharmacology expertise across clinical-stage programs, with a strong focus on pharmacokinetics (PK), pharmacodynamics (PD), and PK/PD analyses to inform clinical development and regulatory decision‑making. The position requires strong scientific expertise, critical thinking, and the ability to independently interpret and integrate complex clinical pharmacology data within a highly matrixed environment. The Associate Director partners closely with Research, Clinical Development, Bioanalytical, Regulatory, Project Management, and other R&D functions, contributing to clinical study design, data analysis, regulatory submissions, and scientific publications in support of advancing innovative RNAi therapies. This is a virtual role based in The Netherlands or UK.
Key Responsibilities
- Represent independently Clinical Pharmacology and provide clinical pharmacology support and guidance to clinical stage project teams.
- Lead the analysis, interpretation, integration and reporting of clinical pharmacology data.
- Conduct PK and PK/PD analyses to guide clinical development decisions.
- Provide clinical pharmacology input for regulatory submissions such as briefing documents, IND, CTA and NDA.
- Prepare and input independently appropriate documents or sections of clinical protocols, Investigator Brochures, Clinical Study Reports with respect to Clinical Pharmacology studies or data.
- Closely partner with Research, Bioanalytical, Clinical, Regulatory, Project Management, and other R&D functions.
- Preparation of abstracts and manuscripts for publications.
Qualifications
- Ph.D. (or Pharm.D.) in relevant field (i.e. Pharmacokinetics, Pharmacometrics, Clinical Pharmacology) with in depth experience in pharmaceutical/biotech industry.
- 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.
- Proficient in using Phoenix WinNonlin, R, NONMEM, or other pharmacokinetic, modeling and data visualizations software.
- Ability to function in a highly matrixed team environment is essential.
- Ability to work independently.
- Strong communication and presentation skills (verbal and written).
- Excellent interpersonal skills and ability to work independently.
- Fluency in English (verbal and written).
Why Alnylam? Join a company recognized for its innovation, open culture, and commitment to people. At Alnylam, you'll work in an environment that values collaboration, purpose, and excellence - and be part of a team bringing groundbreaking RNAi therapies to patients in need.
Associate Director, Clinical Pharmacology employer: Alnylam Pharmaceuticals, Inc.
Alnylam Pharmaceuticals is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of the UK. Employees benefit from comprehensive professional development opportunities, competitive compensation, and a commitment to work-life balance through hybrid working arrangements. Join us to be part of a pioneering team dedicated to advancing healthcare solutions while enjoying a supportive environment that values your contributions.
Contact Details:
Alnylam Pharmaceuticals, Inc. Recruitment Team
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