Freelance Senior Clinical Research Associate (Turkey)

ProPharma Group; Turkey; Remote; TRY 150,000 - 230,000; Full time

Job summary

ProPharma Group is seeking a Senior Clinical Research Associate to join as a freelance contributor at 0.5 FTE for a site in Turkey. The role covers clinical monitoring, site initiation, and close-out activities, ensuring studies conform to protocol, SOPs, GCP, and regulatory requirements.

Key responsibilities include monitoring visits (in person and remote), regulatory document reviews, and site qualification activities, with strong emphasis on data integrity and study conduct.

Qualifications

• Excellent verbal and written communication skills.
• Strong organizational and documentation abilities.
• Knowledge of GCP and ICH guidelines.
• Experience with EDC/CTMS systems is required.

Responsibilities

• Monitor assigned sites according to protocol, SOPs and GCP.
• Prepare monitoring visit reports and ensure regulatory compliance.
• Coordinate site startup activities and site feasibility assessments.
• Maintain site documentation, tracking, and regulatory submissions.

Skills

Excellent communication

MS Office proficiency

Regulatory knowledge

Prioritization & planning

Site coordination

Education

Bachelor's degree

Tools

EDC

CTMS

IVRS

eTMF

Job description

ProPharma Group is seeking a Senior Clinical Research Associate to join as a freelance contributor at 0.5 FTE for a site in Turkey. The role covers clinical monitoring, site initiation, and close-out activities, ensuring studies conform to protocol, SOPs, GCP, and regulatory requirements.

Key responsibilities include monitoring visits (in person and remote), regulatory document reviews, and site qualification activities, with strong emphasis on data integrity and study conduct.