Senior Clinical Scientist

ICON plc

Senior Clinical Scientist advancing hematology-oncology medicines for ICON, a global clinical research organisation. Leading early-development and clinical-pharmacology studies, regulatory submissions, and cross-functional scientific strategy.

Posted 8/18/2026full-timeRemote • North Carolina, Pennsylvania, Texas • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical pharmacology and early clinical development, with a strong ability to author and review clinical protocols, regulatory submissions, and study reports. Proven track record in collaborating with cross-functional teams and managing clinical studies while ensuring compliance with scientific standards and regulatory requirements.

Highest-signal resume keywords

Clinical Pharmacology ExpertiseEarly Phase/Phase I ExperienceRegulatory Submissions (INDs, Amendments)Excellent Written and Oral Communication SkillsAbility to Analyze Problems and Provide Solutions

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Protocol DevelopmentClinical Study ExecutionData Analysis and SummarizationRegulatory ComplianceClinical Safety and Efficacy ReviewProject ManagementStatistical Analysis CollaborationScientific Manuscript AuthoringBudget ManagementTimelines Adherence

Soft Skills

Creative Problem SolvingInfluencing Matrix TeamsIndependent WorkMulti-Priority ManagementCollaborative Relationship Building

Certifications & Qualifications

PhDPharmDMDBSMS

Industry Keywords

Clinical DevelopmentImmunologyOncologySOPsHealth Authority SubmissionsTranslational SciencesQuantitative Clinical PharmacologyConsultant CollaborationScientific StandardsCompetitive Landscape Knowledge

About the role

Key responsibilities & impact

Provide strategic leadership and demonstrate accountability for clinical programs supporting early clinical development and clinical pharmacology
Maintain knowledge of the competitive landscape, current assets, and evolving standards of care
Provide subject matter expertise on cross-functional project teams
Author, review, and approve clinical protocols, analysis plans, study reports, and regulatory submissions
Execute clinical and clinical pharmacology studies with Clinical Operations
Review and summarize clinical safety and efficacy data with the Medical Monitor
Collaborate with Quantitative Clinical Pharmacology, Translational Sciences, and Statistics to develop protocols and summarize analyses
Contribute to program strategy for assigned compounds and programs, including clinical development plans
Draft and review INDs, IND amendments, Investigator Brochures, Annual Reports, and other Health Authority submissions
Ensure adherence to timelines, budgets, scientific standards, regulatory requirements, and SOPs
Develop collaborative relationships with consultants and external experts
Participate in project teams and liaise with project teams, CROs, Clinical sub-teams, and other stakeholders
Present data at internal and external scientific meetings
Author manuscripts for scientific journals

Requirements

What you’ll need

At least 5 years’ experience with a PhD, PharmD, or MD degree
Alternatively, at least 10 years’ experience with a BS/MS degree emphasizing early development, clinical pharmacology, or a related discipline
Experience in early development, clinical pharmacology, or a related discipline
Ability to critically analyze problems and provide creative solutions
Excellent written and oral communication skills
Ability to present to and influence matrix teams and senior leaders
Ability to work independently and manage multiple priorities in a dynamic environment
Experience in clinical pharmacology, immunology, or oncology preferred
Early phase/Phase I experience required
Willingness to travel up to 20%
Legal right to work in the country where the role is based
Ability to work in compliance with departmental and organizational SOPs, scientific standards, and regulatory requirements

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
Accommodations available for individuals with disabilities
Reasonable accommodations during the recruitment process
Opportunity to contribute to a diverse, inclusive, and accessible workplace
Opportunity to make a difference to patients’ lives
Sustainable business practices and community support