Senior) Clinical Research Associate - Sponsor-Dedicated
Location : Turkey (Nationwide) - Istanbul or Izmir are preferred locations
Employment Type : Full-time, Permanent
Join a leading global CRO, currently partnering with a major sponsor on long-term clinical trials across multiple therapeutic areas. This is a position offering the structure, training, and support of a global organization, while providing the opportunity to work closely with one client and gain deep exposure to their studies and systems.
Key Responsibilities :
- Conduct site selection, initiation, monitoring, and close-out visits
- Ensure compliance with GCP, ICH guidelines, and local regulations
- Support patient recruitment and site performance strategies
- Track regulatory submissions, case report forms (CRFs), and data query resolution
- Collaborate closely with investigators, study site staff, and sponsor stakeholders
Requirements :
Degree in a life sciences or healthcare-related fieldPrevious working history within independent on-site monitoringStrong knowledge of clinical research regulations and GCPFluent in Turkish and English (written and verbal)Proficient in MS OfficeExcellent organizational and time management skillsAbility to build strong site and internal relationshipsFlexibility to travel as requiredValid driver's license (Class B)What's on Offer :
Dedicated training and mentoring programs to support career developmentAccess to global resources and operational supportExposure to a wide range of therapeutic areas and study phasesFlexible work-life balanceCompetitive salary, company car, phone, and comprehensive benefits packageStable role with an international CRO and long-term client partnership