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ICON plc

Publications and Scientific Communications Lead

ICON plc

. Manage the scientific and operational aspects of clinical research projects, ensuring adherence to protocols and timelines .

Posted 10/9/2026full-timeBlue Bell • Pennsylvania • United StatesSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in managing clinical research projects, focusing on scientific methodologies, data analysis, and regulatory compliance. Proven ability to lead cross-functional teams and ensure high-quality data collection and project deliverables.

Highest-signal resume keywords
Clinical Research ManagementProject ManagementData AnalysisRegulatory ComplianceCross-Functional Team Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Scientific MethodologiesStudy DesignData CollectionData InterpretationAnalytical Tools
Soft Skills
LeadershipOrganizational SkillsCommunicationInterpersonal SkillsStakeholder Influence
Industry Keywords
Clinical ResearchResearch StrategiesRegulatory AgenciesProject LifecycleResearch Partners

About the role

Key responsibilities & impact
  • Manage the scientific and operational aspects of clinical research projects, ensuring adherence to protocols and timelines
  • Collaborate with cross-functional teams to develop and implement research strategies and solve complex scientific challenges
  • Oversee the design, execution, and analysis of study protocols, ensuring high-quality data collection and interpretation
  • Provide guidance and support on scientific methodologies, data analysis, and regulatory compliance throughout the project lifecycle
  • Build and maintain relationships with research partners and regulatory agencies to advance project goals and drive innovation
  • Oversee scientific operations workstreams, ensuring deliverables meet quality and timeline expectations

Requirements

What you’ll need
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Proven experience in managing scientific aspects of clinical research, with a strong focus on project management and data analysis
  • Strong leadership and organizational skills, with experience in leading cross-functional teams and managing complex projects
  • Expertise in scientific methodologies, study design, and regulatory requirements, with proficiency in relevant analytical tools
  • Excellent communication and interpersonal skills, with the ability to influence stakeholders and ensure successful project outcomes
  • 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