Senior Clinical Research Associate

Michael Page Türkiye; Fatih; On-site; TRY 50,000 - 70,000; Full time

Job summary

A leading global clinical research organization is seeking a Senior Clinical Research Associate in Istanbul. This role involves site selection, monitoring, and regulatory compliance. The ideal candidate will have a scientific background, with significant monitoring experience and strong command of both Turkish and English.

Qualifications

• At least 2 years of independent on-site monitoring experience.
• Solid understanding of ICH-GCP guidelines and local regulations.
• Proficiency in Microsoft Office applications.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits.
• Support development of a subject recruitment plan.
• Evaluate quality and integrity of site practices according to GCP.

Skills

Communication

Organizational skills

Problem-solving

Turkish proficiency

English proficiency

Education

University degree in scientific discipline or health-related field

Tools

Microsoft Office

Job description

• A Global Company in Healthcare Sector
• Great Opportunity

About Our Client

• We are supporting a leading global clinical research organization in their search for an experienced Senior Clinical Research Associate to lead site monitoring and clinical operations in Turkey.

Job Description

• Performing site selection, initiation, monitoring and close-out visits
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• Collaborating with experts at study sites and with client representatives

The Successful Applicant

• University degree in a scientific discipline or health-related field
• At least 2 years of independent on-site monitoring experience
• Solid understanding of ICH-GCP guidelines and local regulatory landscape
• Proficiency in Microsoft Office applications
• Excellent command of Turkish and English
• Strong communication, organizational, and problem-solving skills
• Ability to establish effective working relationships with site staff, colleagues, and sponsor contacts
• Willingness to travel; valid driver's license

What's on Offer

If you are passionate about clinical research and seeking a rewarding opportunity in Istanbul, we encourage you to apply today!