Clinical Research Jobs at ICON
ICON plc is hiring a Clinical Research Associate II (Senior CRA) to join its Strategic Solutions Clinical Monitoring team in Ankara, Turkey. The Clinical Research Jobs at ICON plc Careers are ideal for experienced CRAs who are passionate about clinical research excellence, patient safety, and regulatory compliance. As a Senior CRA, you will play a pivotal role in ensuring the successful execution of clinical trials across their full lifecycle.
Job Details:
- Job Title: Clinical Research Associate II (Senior CRA)
- Job Reference ID: JR139417
- Location: Ankara, Turkey
- Employment Type: Full-Time
- Work Mode: Remote / Field-Based
- Department: Clinical Monitoring – ICON Strategic Solutions
- Travel Requirement: Up to 60% (domestic and international)
About the Company:
ICON plc is a global leader in healthcare intelligence and clinical research, partnering with pharmaceutical, biotechnology, and medical device companies to accelerate the development of life-saving treatments. With a strong commitment to inclusion, innovation, and scientific excellence, ICON provides a collaborative environment where professionals can grow and make a meaningful impact on global health.
Educational Requirements for Clinical Research Jobs:
- Advanced degree in Life Sciences, or a related discipline
- Extensive hands-on experience as a Clinical Research Associate
- Strong knowledge of clinical trial regulations and global compliance standards
Key Responsibilities:
- In Clinical Research Jobs, you have to monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements
- Conduct on-site and remote monitoring visits to evaluate site performance and resolve issues
- Ensure accurate, timely, and high-quality clinical data collection and reporting
- Collaborate with cross-functional teams to support trial milestones and deliverables
- Train and mentor site staff and junior CRAs on clinical trial best practices
- Build and maintain strong relationships with investigators, site teams, and stakeholders
- Safeguard participant safety and data integrity throughout the study lifecycle
Skills Required:
- In-depth knowledge of ICH-GCP guidelines and clinical trial regulations are required for the Clinical Research Jobs at ICON plc Careers.
- Strong site management, monitoring, and risk assessment skills
- Ability to manage multiple studies and sites simultaneously
- Proficiency with clinical trial systems and monitoring tools
- Excellent communication, interpersonal, and stakeholder management skills
- Strong problem-solving and organizational abilities
- Valid driver’s license and willingness to travel extensively
Benefits of the Clinical Research Jobs at ICON plc Careers:
- Competitive salary package
- Comprehensive, country-specific benefits
- Generous annual leave entitlements
- Health insurance coverage for employees and families
- Retirement and long-term financial planning options
- Global Employee Assistance Program (LifeWorks)
- Flexible benefits including childcare support, gym memberships, travel subsidies, and wellness programs
- Inclusive, diverse, and supportive workplace culture
