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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial monitoring, ensuring adherence to regulatory requirements and Good Clinical Practice (GCP) standards while effectively managing multiple sites and projects. Strong communication and interpersonal skills facilitate collaboration with cross-functional teams and site personnel.
Highest-signal resume keywords
Clinical Trial MonitoringGood Clinical Practice (GCP)Site ManagementData IntegrityOphthalmology Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ProcessesRegulatory RequirementsMonitoring PracticesProblem-SolvingOrganizational Skills
Soft Skills
Communication SkillsInterpersonal SkillsStakeholder ManagementInfluencing Skills
Tools & Technologies
Clinical Trial Software
Industry Keywords
Clinical Research AssociateSite VisitsData CollectionTrial ExecutionHouston Area
About the role
Key responsibilities & impact- Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
- Conduct site visits to assess site performance, resolve issues, and provide support for successful trial execution
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs
- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations
Requirements
What you’ll need- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
- Experience monitoring complex indication in Ophthalmology
- Willingness to travel as required (approximately 60%)
- Candidates must be located in the greater Houston area
- 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