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ICON plc

Clinical Pharmacologist

ICON plc

. Ensure all medical team activities comply with current local and international regulations, laws, guidance, Good Clinical Practices, company standards, policies and procedures, and the Principles of Medical Research .

Posted 11/11/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Clinical Pharmacology and regulatory compliance, with a strong focus on delivering high-quality clinical studies and submissions. Proficient in collaborating across functions to support clinical development strategies and ensure adherence to Good Clinical Practices.

Highest-signal resume keywords
Clinical Pharmacology ExpertiseRegulatory Submission PlanningGood Clinical Practices (GCP)Interpersonal Communication SkillsTeam Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical PharmacologyPharmacokineticsStudy Protocol DevelopmentBiopharm Submission PlansClinical Study DesignData Collection RequirementsBiomarker QualificationPhase I and II Clinical StudiesStatistical AnalysisDrug-Disease Response Models
Soft Skills
Negotiation SkillsOrganizational SkillsInfluencing SkillsTeamwork Skills
Certifications & Qualifications
Life Science Degree (MD, PhD, PharmD)
Industry Keywords
Good Clinical PracticesClinical DevelopmentRegulatory ComplianceClinical TrialsMarket DifferentiationHealth Outcomes ResearchExecutive PresentationsKey Opinion Leader InteractionsClinical Candidate SelectionDomestic and International Travel

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Ensure all medical team activities comply with current local and international regulations, laws, guidance, Good Clinical Practices, company standards, policies and procedures, and the Principles of Medical Research
  • Participate in internal executive and governance presentations, external key opinion leader interactions, medical outreach/advocacy, and industry conferences
  • Deliver clinical pharmacology and pharmacokinetics work to a high standard
  • Contribute to overall strategy and clinical plans for development of clinical compounds, focusing on studies required for product decisions or regulatory submissions
  • Support high-level plans for Phase 2 and 3 studies and detailed biopharm plans for submissions
  • Collaborate with Global Patient Safety, PK/PD, ADME, Statistics, Tailored Therapeutics and other quantitative science functions
  • Integrate study development and conduct with disease-progression and drug-disease response models
  • Contribute to global Phase I and II clinical studies and submission planning
  • Work with discovery research scientists on basic research strategies, clinical candidate selection and preclinical development
  • Provide market differentiation and regulatory support in biopharm submission plans
  • Design and oversee clinical pharmacology, biomarker qualification and development studies
  • Develop, create and oversee study protocols and supporting documents in accordance with GCP and local requirements
  • Collaborate with clinical research staff, statisticians, health outcomes research scientists, consultants and investigators on protocols and data collection requirements
  • Participate in investigator identification and selection

Requirements

What you’ll need
  • Life science degree (MD, PhD, PharmD) with requisite experience in Clinical Pharmacology
  • Experience in Clinical Pharmacology
  • Fluent in English; both written and verbal communications
  • Interpersonal, organizational and negotiation skills
  • Ability to influence others (both cross-functionally and within the function) in order to create a positive working environment
  • Excellent teamwork skills
  • Willing to engage in domestic and international travel to the degree appropriate to support the business of the team
  • Employment with ICON is contingent upon having the legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways