Remote Senior CRA (0.5 FTE) - Turkey

ProPharma Group; Turkey; On-site; TRY 180,000 - 300,000; Full time

Job summary

ProPharma is seeking a Senior Clinical Research Associate to join on a freelance basis at 0.5 FTE to support a site in Turkey. The role ensures monitoring activities are conducted in accordance with the study protocol, SOPs, GCP and local regulations, including site initiation and regulatory submissions.

The candidate will perform on-site and remote monitoring, review source documents, manage supplies, and coordinate with investigators and cross-functional teams to maintain data integrity and

Qualifications

• Bachelor's degree or equivalent combination of education and experience.
• 5+ years of experience as a Clinical Research Associate.
• Experience in site monitoring, data review, and regulatory documentation.

Responsibilities

• Monitor clinical sites for protocol compliance and GCP.
• Perform on-site and remote monitoring visits; prepareMonitoring reports.
• Assist with study start-up activities, site initiation, ethics submissions.
• Coordinate regulatory documents and site tools; ensure data integrity.
• Manage investigational supplies, inventory, and reconciliation.
• Communicate with investigators, sites, and cross-functional teams.

Skills

Communication skills

MS Office

EDC/CTMS/eTMF

ICH/GCP regulatory knowledge

Site monitoring experience

Problem solving

Training/mentoring

Education

Bachelor's degree or equivalent

Tools

EDC systems

CTMS

IVRS

eTMF

Job description

ProPharma is seeking a Senior Clinical Research Associate to join on a freelance basis at 0.5 FTE to support a site in Turkey. The role ensures monitoring activities are conducted in accordance with the study protocol, SOPs, GCP and local regulations, including site initiation and regulatory submissions.

The candidate will perform on-site and remote monitoring, review source documents, manage supplies, and coordinate with investigators and cross-functional teams to maintain data integrity and