Principal Scientist

SRG; Slough; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global biopharmaceutical leader is seeking a Principal Scientist (PKPD) to lead non-clinical PKPD strategy and oversee GLP toxicokinetics studies. The role involves delivering regulatory data packages and collaborating with cross-functional teams. Candidates should have a PhD/MSc/BSc in Pharmacology or related fields and 5+ years of PKPD data analysis experience. Strong pharmacology knowledge and GLP experience are essential.

Qualifications

• PhD/MSc/BSc in Pharmacology, PKPD, DMPK or related field.
• 5+ years’ hands-on PKPD data analysis in pharma/CRO.
• Strong pharmacology knowledge and GLP experience.
• Proficient in Phoenix WinNonlin.

Responsibilities

• Lead non-clinical PKPD strategy in the Quantitative Clinical Pharmacology function.
• Design and oversee GLP toxicokinetics studies.
• Deliver high-quality regulatory data packages.
• Collaborate with cross-functional teams and CROs to drive drug development.

Skills

PKPD data analysis

Strong pharmacology knowledge

GLP experience

Excellent communication skills

Education

PhD/MSc/BSc in Pharmacology or related field

Tools

Phoenix WinNonlin

R

Berkeley Madonna

Job description

Overview

SRG are partnering with a global biopharmaceutical leader seeking a Principal Scientist (PKPD) to join their Quantitative Clinical Pharmacology function. You will lead non-clinical PKPD strategy, design and oversee GLP toxicokinetics studies, deliver high-quality regulatory data packages, and collaborate with cross-functional teams and CROs to drive innovative drug development.

Responsibilities

• Lead non-clinical PKPD strategy within the Quantitative Clinical Pharmacology function.
• Design and oversee GLP toxicokinetics studies.
• Deliver high-quality regulatory data packages.
• Collaborate with cross-functional teams and CROs to advance drug development programs.

Qualifications

• PhD/MSc/BSc in Pharmacology, PKPD, DMPK or related field
• 5+ years’ hands-on PKPD data analysis in pharma/CRO
• Strong pharmacology knowledge and GLP experience
• Proficient in Phoenix WinNonlin (R or Berkeley Madonna a plus)
• Excellent communication and reporting skills

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Science and Research

Industries

• Pharmaceutical Manufacturing