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Senior Clinical Research Associate
ICON Strategic Solutions
Jeddah, KSA
Contract
Senior
Field
4 weeks ago
Clinical Trial MonitoringGood Clinical Practice (GCP)Site ManagementData IntegrityRegulatory ComplianceStakeholder Management
Free
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Clinical Trial MonitoringGood Clinical Practice (GCP)Site Management
About the Role
ICON plc is hiring a Senior Clinical Research Associate based in Saudi Arabia to oversee clinical trial activities. The role involves monitoring sites, ensuring GCP compliance, and collaborating with cross-functional teams.
Key Skills for This Role
Clinical Trial MonitoringGood Clinical Practice (GCP)Site ManagementData IntegrityRegulatory ComplianceStakeholder Management
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
- Proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Willingness to travel as required (approximately 60%)
- Based in Saudi Arabia
Full Job Posting
Role Overview
- ICON plc is a world leading healthcare intelligence and clinical research organization.
- As a Senior CRA, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
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 for 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.
- Proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills.
- Willingness to travel as required (approximately 60%).
- Based in Saudi Arabia.
What ICON Can Offer You
- Competitive salary.
- Various annual leave entitlements.
- Range of health insurance offerings.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme.
- Life assurance.
- Flexible country specific optional benefits.
About ICON
- ICON is committed to providing an inclusive and accessible environment.
- All qualified applicants receive equal consideration for employment.
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