Associate Director, Clinical Pharmacology

Alnylam Pharmaceuticals; United Kingdom; On-site; GBP 70,000 - 110,000; Full time

Job summary

An innovative firm is seeking an Associate Director in Clinical Pharmacology to support a growing portfolio of RNAi therapeutics. This pivotal role involves leading data analysis and interpretation to inform clinical development, while collaborating with various teams to ensure successful regulatory submissions. Candidates should possess a Ph.D. or Pharm.D. and demonstrate expertise in clinical pharmacology and data analysis. Join a company that values innovation and diversity, and be part of a mission to transform lives through groundbreaking therapies.

Qualifications

• Ph.D. or Pharm.D. required with deep knowledge of clinical pharmacology.
• Proficiency in PK modeling and simulation tools.

Responsibilities

• Lead analysis and reporting of clinical pharmacology data.
• Collaborate with cross-functional teams for regulatory submissions.

Skills

Clinical Pharmacology

Data Analysis

Critical Thinking

Communication Skills

PK and PD Analysis

Education

Ph.D. or Pharm.D. in Pharmacokinetics

Industry Experience

Tools

Phoenix WinNonlin

R

NONMEM

Job description

Associate Director, Clinical Pharmacology

Employer: Alnylam Pharmaceuticals

Location: United Kingdom

Salary: Competitive

Closing date: 3 May 2025

Categories: Life Sciences, Pharmacology

Hours: Full Time

Result Type: Jobs

Position Overview

The Associate Director in Clinical Pharmacology will support a rapidly expanding clinical portfolio of RNAi therapeutics in CNS. The ideal candidate should have expertise in clinical pharmacology, PK, and PD, with strong data analysis skills. This role requires critical thinking, excellent communication skills, and the ability to work independently in a matrixed environment.

Key Responsibilities

• Represent Clinical Pharmacology independently and support clinical stage project teams.
• Lead analysis, interpretation, and reporting of clinical pharmacology data.
• Conduct PK and PK/PD analyses to inform clinical development decisions.
• Contribute to regulatory submissions, including briefing documents, IND, CTA, and NDA.
• Prepare sections of clinical protocols, Investigator Brochures, and Clinical Study Reports related to Clinical Pharmacology.
• Collaborate with Research, Bioanalytical, Clinical, Regulatory, and Project Management teams.
• Prepare abstracts and manuscripts for publication.

Qualifications

• Ph.D. or Pharm.D. in Pharmacokinetics, Pharmacometrics, or Clinical Pharmacology with industry experience.
• Deep knowledge of clinical pharmacology, PK, modeling, and simulation.
• Familiarity with international guidelines related to Clinical Pharmacology and Pharmacometrics.
• Proficiency in Phoenix WinNonlin, R, NONMEM, or similar software.
• Ability to work effectively in a matrixed team and independently.
• Strong communication and presentation skills.
• Fluent in English, both verbal and written.

About Alnylam

Alnylam Pharmaceuticals (Nasdaq: ALNY) pioneers RNAi therapeutics, transforming lives with innovative medicines based on Nobel Prize-winning science. Founded in 2002, we lead the RNAi Revolution, turning scientific possibilities into real-world treatments.

Our Culture

We foster a people-first culture guided by values of innovation, openness, urgency, excellence, and inclusivity. Recognized as a top employer globally, we prioritize diversity and equal opportunity, ensuring all employees can thrive and bring their authentic selves to work.

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