Clinical Research Associate Job at ICON | Remote Job for Medicine Graduates
The clinical research associate job at ICON offers a unique opportunity for experienced professionals to contribute to high-quality global clinical trials. This remote job focuses on clinical monitoring, regulatory compliance, and site management while working with one of the world’s leading healthcare organizations. Explore how ICON careers can help advance your clinical research expertise.
Clinical Research Associate Job Details:
- Job Title: Clinical Research Associate II
- Location: Ankara
- Job Reference: JR139417
- Department: Clinical Monitoring
- Organization: ICON Strategic Solutions
- Work Type: Remote
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment, driving innovation and excellence. Explore ICON careers to join a team shaping the future of clinical development through innovative clinical trials.
Qualifications
- An advanced degree in a relevant field, such as medicine
- Extensive experience as a CRA, with a strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management, including proficiency in relevant clinical trial tools
- Excellent communication and stakeholder management skills
- Ability to travel at least 60% of the time (international and domestic – fly and drive) with a valid driver’s license
Clinical Research Associate Job Description
This clinical research associate role is a Senior Clinical Research Associate (CRA) within ICON Strategic Solutions. As a Senior CRA at ICON Plc, the role is critical to overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. This remote job contributes to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
Key Responsibilities
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
- Building and maintaining effective relationships with site personnel and stakeholders to support smooth trial operations
