Senior Clinical Research Associate — Remote

Parexel International; Turkey; On-site; TRY 180,000 - 240,000; Full time

Job summary

Parexel International partners with biopharmaceutical companies to deliver patient-focused clinical trials across Turkey. The role focuses on monitoring responsibilities, site activation and ongoing study execution to ensure high quality data and compliant conduct.

The candidate should have extensive trial methodologies knowledge, 3+ years in site monitoring ( Oncology preferred), strong English, and willingness to travel nationwide in Turkey.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local regulations.
• Experience coordinating monitoring activities and site management.
• Global trial exposure and willingness to travel across Turkey.
• Fluency in English and ability to work with multinational teams.

Responsibilities

• Ensure proper conduct of clinical trials per SMP and applicable laws, to meet timelines and quality.
• Manage operational aspects from site activation to database lock with quality deliverables.
• Serve as primary contact for investigator sites; collaborate with SCP for site delivery quality.
• Attend investigator meetings; provide enrollment support and address site activation/recruitment issues.
• Conduct onsite/remote monitoring; ensure compliance with SOPs and SMP during study activities.
• Monitor site AEs/SAEs; coordinate with Drug Safety for SAE resolution.
• Submit required reports and documentation (TMF, site reports, protocol deviations, recruitment).
• Identify and resolve site issues; implement corrective actions to prevent recurrence.
• Prepare site close-out plans and complete close-out activities on time.

Skills

Clinical trial methodologies

ICH/GCP regulatory knowledge

Monitoring experience

Oncology experience

Global clinical trials

Fluent English

Travelling in Turkey

Driver's license & passport

Education

Bachelor’s degree in life sciences

Job description

Parexel International partners with biopharmaceutical companies to deliver patient-focused clinical trials across Turkey. The role focuses on monitoring responsibilities, site activation and ongoing study execution to ensure high quality data and compliant conduct.

The candidate should have extensive trial methodologies knowledge, 3+ years in site monitoring ( Oncology preferred), strong English, and willingness to travel nationwide in Turkey.