Head of Clinical Pharmacology

RBW Consulting; Liverpool; On-site; GBP 70,000 - 90,000; Full time

Job summary

A leading biotech company in Liverpool is seeking an experienced Clinical Pharmacologist to shape strategy and execute clinical programs. This role involves defining pharmacology strategies, overseeing critical studies, and collaborating with regulatory bodies. Candidates should have an advanced degree and over 10 years of experience in clinical pharmacology, with proven leadership skills. Strong communication abilities are essential for interaction with cross-functional teams. This is a high-impact position vital for the company's development portfolio.

Qualifications

• 10+ years in clinical pharmacology with small molecules.
• Expertise in clinical pharmacology study design and regulatory documentation.

Responsibilities

• Define and implement clinical pharmacology strategies.
• Oversee first-in-human and drug-drug interaction studies.
• Contribute to IND, End-of-Phase 2, and NDA submissions.

Skills

Clinical pharmacology expertise

PK / PD modeling

Strong communication skills

Education

Advanced degree (PharmD, PhD or equivalent)

Job description

RBW is seeking an accomplished Clinical Pharmacologist to play a pivotal role in shaping strategy and driving execution across a dynamic biotech’s development portfolio. In this high-impact position, you’ll be the leading authority on clinical pharmacology—developing innovative strategies, guiding study design, and integrating PK / PD and preclinical data into clinical development plans. You’ll influence critical decisions, oversee first-in-human and drug–drug interaction studies, and represent the company in regulatory interactions and external collaborations.

What You’ll Do

• Define and implement clinical pharmacology strategies across early and late-stage programs.
• Oversee first-in-human and drug–drug interaction studies, PK / PD modeling, and dose selection for Phase 2 / 3 trials.
• Contribute to IND, End-of-Phase 2, and NDA submissions, and represent the function in regulatory meetings.
• Work closely with preclinical, clinical, and CMC teams to optimise study design.

What We’re Looking For

• Advanced degree (PharmD, PhD or equivalent)
• 10+ years in clinical pharmacology with small molecules
• Expertise in PK / PD modeling, clinical pharmacology study design, and regulatory documentation
• Proven leadership in global, cross-functional teams
• Strong English communication and writing skills