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Senior Clinical Research Associate
ICON plc
Riyadh, KSA
Full Time
Senior
Field
4 weeks ago
Clinical Trial MonitoringGood Clinical Practice (GCP)Site ManagementData IntegrityRegulatory ComplianceCommunication
Free
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Clinical Trial MonitoringGood Clinical Practice (GCP)Site Management
About the Role
ICON plc seeks a Senior Clinical Research Associate to oversee clinical trial activities in Riyadh. The role involves monitoring trial sites, ensuring GCP compliance, and collaborating with cross-functional teams.
Key Skills for This Role
Clinical Trial MonitoringGood Clinical Practice (GCP)Site ManagementData IntegrityRegulatory ComplianceCommunication
Responsibilities
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards
- Conduct site visits to assess site performance, resolve issues, and provide support
- 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
Requirements
- Bachelor's degree in a relevant scientific discipline or healthcare related field
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and site management
- Excellent communication, interpersonal, and stakeholder management skills
- Willingness to travel approximately 60%
- Based in Saudi Arabia
Full Job Posting
Role Overview
- ICON is a global healthcare intelligence and clinical research organisation.
- As a Senior CRA, you will oversee and manage clinical trial activities.
What You Will Do
- Lead on clinical trial monitoring tasks requiring technical depth.
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
- Conduct site visits to assess site performance, resolve issues, and provide support.
- 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.
Your Profile
- Bachelor's degree in a relevant scientific discipline or healthcare related field.
- Extensive experience as a Clinical Research Associate.
- Proven ability to manage multiple sites and projects simultaneously.
- Expertise in monitoring practices, data integrity, and site management.
- Excellent communication, interpersonal, and stakeholder management skills.
- Willingness to travel as required (approximately 60%).
- Based in Saudi Arabia.
Rewards & Benefits
- 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.
Inclusion and Accessibility
- ICON is an equal opportunity employer committed to building an inclusive and accessible workplace.
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