Senior Clinical Associate
On-site · Istanbul, Istanbul, Turkey
Job Summary
Lead on clinical coordination tasks with a focus on quality and continuous improvement. Manage and coordinate clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines. Collaborate with cross-functional teams to address clinical trial issues, optimize processes, and ensure effective execution of studies. Oversee site management and monitoring to ensure data integrity and compliance with study protocols. Provide guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards. Track and report on trial progress, identify potential risks, and implement strategies to mitigate challenges.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders
- Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges
Additional Requirements
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
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