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Senior Pk Scientist

Icon Plc
ICON PLC
4+ years
Not Disclosed
Remote
10 March 18, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior PK Scientist – Clinical Pharmacology (PK/PD Analysis)

Location: Remote (UK – Livingston | Netherlands – Assen | France – Paris | India – Bangalore | Spain – Madrid | Multiple Global Locations)
Job Type: Full-Time
Company: ICON plc
Job ID: JR146673

About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a highly skilled Senior PK Scientist to support clinical pharmacology activities across Phase I–IV clinical trials. This remote role offers the opportunity to work on global drug development programs, focusing on PK/PD analysis, protocol development, and regulatory reporting.

Key Responsibilities

  • Lead authoring and coordination of clinical pharmacology trial protocols

  • Perform PK, PD, and PK/PD analyses using non-compartmental analysis (NCA) methods

  • Develop Clinical Pharmacology Analysis Plans (CPAP) and data handling documentation

  • Generate tables, listings, and figures (TLFs)

  • Contribute to Clinical Study Reports (CSRs), particularly clinical pharmacology sections

  • Conduct quality control (QC) reviews of protocols, datasets, and outputs

  • Ensure compliance with ICH-GCP, SOPs, and regulatory requirements

  • Collaborate with cross-functional teams including biostatistics and data management

Required Qualifications & Experience

  • Bachelor’s degree or higher in Life Sciences, Pharmacology, or a related field

  • Minimum 4+ years of experience in clinical pharmacology or PK/PD analysis

  • Strong expertise in non-compartmental analysis (NCA)

  • Hands-on experience with Phoenix WinNonlin

  • Working knowledge of R programming (preferred)

  • Understanding of clinical trial protocols and regulatory standards

  • Strong data handling and database knowledge

  • Excellent communication and documentation skills

Preferred Skills

  • Experience across Phase I–IV clinical trials

  • Exposure to advanced PK/PD modeling techniques

  • Experience in regulatory submissions and reporting

Why Join ICON
ICON offers a collaborative and inclusive work environment with strong focus on innovation and career development.

Key Benefits Include

  • Competitive salary and global exposure

  • Generous leave policies

  • Health and wellness benefits

  • Retirement planning support

  • Employee Assistance Programme (24/7 support)

  • Life insurance

  • Flexible, country-specific benefits

Diversity, Equity & Inclusion
ICON is an equal opportunity employer committed to a diverse and inclusive workplace. All qualified applicants will be considered without discrimination.

Application Note
Candidates who do not meet all requirements are still encouraged to apply. ICON values potential and diverse professional backgrounds.