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Regulatory Technician
ICON plcRegulatory Technician preparing and maintaining regulatory submission documentation at ICON, a global clinical research organisation. Supporting health authority interactions and clinical research operations.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in preparing and managing regulatory documents and submissions, ensuring compliance with established standards and quality checks. Proficient in cross-functional collaboration and maintaining accurate regulatory trackers and filing systems.
Highest-signal resume keywords
Regulatory Document PreparationRegulatory Affairs SupportClinical Research KnowledgeAttention to DetailWritten and Verbal Communication
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Regulatory Document CompilationQuality Checks on DocumentsRegulatory Trackers ManagementSubmission CoordinationClinical Terminology Knowledge
Soft Skills
Problem SolvingIndependent WorkCommunication Abilities
Industry Keywords
PharmaBiotechCROHealthcareRegulatory Operations
About the role
Key responsibilities & impact- Prepare, format, and compile regulatory documents and submission components according to established templates and standards
- Maintain regulatory trackers, databases, and filing systems to ensure documents are current, accurate, and inspection-ready
- Support coordination of regulatory submissions by gathering required information from cross-functional teams
- Perform quality checks on documents for completeness, consistency, and adherence to style and formatting requirements
- Assist with management of correspondence and documentation related to health authority interactions
- Contribute to continuous improvement of regulatory operations processes, tools, and templates
Requirements
What you’ll need- Bachelor's degree or High School diploma, ideally in a relevant scientific discipline or healthcare-related field
- Proficiency in English language is required - written, spoken an verbal
- Experience in administration, ideally supporting regulatory affairs within pharma, biotech, or CRO environments
- Ideally 1-2 years relevant experience within clinical research or knowledge of clinical terminology and documentation
- Strong ability to problem solve and work independently
- Outstanding written and verbal communication abilities
- Meticulous attention to detail
- 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