Clinical Research Jobs at ICON plc in Turkey
ICON is seeking a Clinical Site Associate (In-House CRA) based in Ankara to support clinical trial operations through effective site coordination, documentation management, and compliance oversight. The candidate selected for Clinical Research Jobs at ICON plc in Turkey plays a key role in ensuring trial quality, data integrity, and regulatory compliance, while supporting CRAs and maintaining strong site relationships.
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization. The company partners with pharmaceutical, biotechnology, and medical device organizations to advance clinical development and improve patient outcomes. ICON is committed to fostering an inclusive, innovative, and high-performance culture while shaping the future of clinical research worldwide.
Job Details:
- Job Title: Clinical Site Associate (In-House CRA)
- Job Reference: JR141310
- Location: Ankara
- Employment Type: Office-based / Hybrid
- Functional Area: Clinical Monitoring – Full Service & Corporate Support
- Travel Requirement: Less than 10% domestic travel
Educational Requirements:
- Bachelor’s degree in life sciences, healthcare, or a related field
- Previous experience in clinical research or a related discipline is preferred
Key Responsibilities:
- Manage site-level communications, trainings, and system access in the Clinical Research Jobs at ICON plc
- Support site readiness activities and follow up on action items
- Maintain Trial Master File (TMF) and Investigator Site File (ISF) accuracy and inspection readiness in the Clinical Research Jobs at ICON plc
- Perform quality control, filing, and tracking of essential documents
- Support subject tracking, data entry oversight, and system maintenance in CTMS and eTMF
- Assist with eCRF UAT testing and clinical sample tracking
- Prepare for audits and inspections, and support CAPA implementation
- Ensure adherence to protocol, GCP, and regulatory requirements in the CRA Role
- Support timely data entry, query resolution, and protocol deviation follow-ups
- Assist with SAE reporting and external data submissions
- Support CRAs in maintaining strong site relationships and act as a backup or primary contact when required
- In the CRA Role, you should monitor key risks and escalate concerns to CRAs or sites
- Assist with safety reporting submissions and institutional or staff change due diligence
Skills Required:
- Strong organizational and time-management skills
- Excellent verbal and written communication skills in English and the local language
- Attention to detail with the ability to prioritize tasks effectively
- Ability to work independently and collaboratively in a fast-paced environment
- Technical proficiency in EDC, CTMS, eTMF, and remote monitoring tools
- Good understanding of GCP, clinical trial processes, and regulatory requirements
Benefits of the Clinical Research Jobs:
- Competitive salary package
- Various annual leave entitlements
- Comprehensive health insurance options for employees and families
- Competitive retirement and savings plans
- Global Employee Assistance Programme (LifeWorks) with 24/7 support
- Life assurance coverage
- Flexible country-specific benefits such as childcare vouchers, gym discounts, bike purchase schemes, subsidized travel, and health assessments
- Inclusive, diverse, and supportive work environment focused on well-being and work-life balance
