Senior CRA
On-site · Ankara, Ankara, Turkey
Job Summary
As a Senior Clinical Research Associate (CRA) at ICON plc, you will oversee and manage clinical trial activities ensuring compliance with protocols, regulatory requirements, and industry standards. Responsibilities include monitoring clinical trial sites, conducting site visits, collaborating with cross-functional teams for accurate data collection, providing training to site staff, and maintaining effective relationships with stakeholders. Required qualifications include an advanced degree in relevant fields, extensive CRA experience, strong organizational skills, expertise in monitoring practices, and excellent communication skills.
Required Qualifications
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices and data integrity
- Ability to influence and drive compliance within a complex environment
Desired Qualifications
- Strong organizational and problem-solving skills
- Proficiency in relevant clinical trial software and tools
- Excellent communication and interpersonal skills
- Ability to travel at least 60% of the time
Additional Requirements
- Ability to travel at least 60% of the time
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