Demonstrates expertise in Clinical Research Coordination, ensuring compliance with ICH-GCP guidelines and ICON's protocols while maintaining accurate study documentation and fostering collaborative relationships with stakeholders. Proficient in conducting independent monitoring visits and evaluating medical data to ensure patient safety.

Highest-signal resume keywords

Clinical Research Associate ExperienceIndependent On-Site MonitoringICH-GCP Guidelines KnowledgeMedical Data EvaluationExcellent Written And Verbal Communication

About the role

Key responsibilities & impact

Coordinate all activities for setting up and monitoring a study
Complete accurate study status reports and maintain study documentation
Perform monitoring activities
Run sponsor-generated queries efficiently and take responsibility for study cost efficiency
Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff
Ensure patient safety and compliance with ICON's procedures, protocols, and regulatory requirements

Requirements

What you’ll need

University degree in medicine, science, or equivalent
Clinical Research Associate experience
Experience conducting independent on-site monitoring visits and Site Initiation Visits (SIVs)
Knowledge of ICH-GCP guidelines
Expertise to review and evaluate medical data
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
Willingness to travel as required (approximately 60%)
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

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

Study CoordinationMonitoring ActivitiesStudy Documentation MaintenanceFeasibility Study PreparationCost Efficiency Management

Soft Skills

Good Social SkillsTimely Query Resolution

Industry Keywords

Patient SafetyRegulatory ComplianceSite Initiation VisitsStakeholder CollaborationTravel Willingness