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ICON plc

Clinical Research Coordinator – Pre-clinical

ICON plc

. Co-ordinate the outsourcing and delivery of preclinical CPSS project activities .

Posted 10/27/2026full-timeRemote • United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Scientific Project Management, particularly in preclinical drug development, with a strong focus on project planning, resource management, and risk management. Proven ability to facilitate communication and collaboration across cross-functional teams while managing multiple priorities effectively.

Highest-signal resume keywords
Scientific Project ManagementPreclinical Drug DevelopmentProject CoordinationProfessional Project Management CertificationCross-Functional Team Collaboration

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project PlanningResource ManagementRisk ManagementBudget MonitoringTimeline Management
Soft Skills
Organisational SkillsPlanning SkillsCommunication Skills
Tools & Technologies
Project Management ToolsBest Practices in Project Management
Certifications & Qualifications
PMPPRINCE2Agile
Industry Keywords
PharmaceuticalBiotechClinical ResearchContinuous ImprovementVendor Management

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Co-ordinate the outsourcing and delivery of preclinical CPSS project activities
  • Support the development, maintenance, and interpretation of cross-functional project plans
  • Monitor timelines, budgets, resources, risks, and project deliverables
  • Facilitate communication and collaboration across project teams and stakeholders
  • Support management of external vendors and outsourced activities
  • Provide guidance on project management processes, tools, and best practices
  • Identify and help resolve day-to-day project challenges and risks
  • Communicate new processes, procedures, and strategies to project teams
  • Contribute to continuous improvement initiatives to enhance project delivery, quality, and efficiency

Requirements

What you’ll need
  • Bachelor's degree in a relevant scientific discipline
  • Experience in Scientific Project Management
  • Experience supporting pre-clinical drug development projects and activities
  • Strong organisational, planning, and communication skills
  • Ability to manage multiple priorities and work effectively within cross-functional teams
  • Understanding of scientific project management principles, including project planning, resource management, and risk management
  • Advanced degree in a relevant scientific field (desirable)
  • Experience within a pharmaceutical, biotech, or clinical research environment (desirable)
  • Experience in project co-ordination, project management, or change management (desirable)
  • Professional project management certification (PMP, PRINCE2, Agile, or equivalent) (desirable)
  • Broad understanding of scientific project management and drug development processes (desirable)
  • 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