Senior Clinical Research Associate

Parexel

Senior Clinical Research Associate overseeing clinical trial operations with a focus on compliance and quality assurance. Managing relationships with investigator sites in clinical research.

Posted 6/23/2026full-timeRemote • 🇹🇷 TurkeySeniorWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

clinical trial monitoringoncology monitoringprotocol complianceclinical trial methodologiesICH guidelinesGCP guidelinesFDA regulationsclinical supply managementreport submissioncorrective action development

Soft Skills

relationship buildingproblem solvingmentoringcoachingcommunicationcollaborationorganizational skillstime managementleadershipcultural understanding

Tools & Technologies

trial master filesmonitoring toolsenrollment tracking systemsclinical research softwaredata management systemsreporting toolscommunication platformsproject management toolssite management systemsvendor management systems

Industry Keywords

clinical researchinvestigator sitespatient welfaresite monitoringglobal clinical trialsmedical practiceslife sciencesnursingpharmacymedicine

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage all operational aspects of clinical trial activities at assigned investigator sites, ensuring timelines and quality deliverables are consistently met
Serve as the primary point of contact for investigator sites, fostering collaborative relationships with site personnel, study teams, and vendors
Conduct thorough site monitoring activities—both onsite and remote—to maintain protocol compliance and safeguard patient welfare
Identify and resolve site issues promptly, develop corrective actions, and support quality event remediation
Partner with study teams to facilitate investigator meetings, provide enrollment support, and drive recruitment initiatives
Submit timely reports, maintain trial master files, track protocol deviations, and monitor clinical supply management
May mentor Clinical Research Associates and coach site personnel on protocol requirements and best practices

Requirements

What you’ll need

Minimum 4 years of relevant clinical research site monitoring experience
1+ years of oncology monitoring experience
Bachelor's degree in life sciences, nursing, pharmacy, medicine, or equivalent professional qualification
Extensive knowledge of clinical trial methodologies, ICH/GCP guidelines, and FDA/local regulations
Fluency in English and Turkish
Valid driver's license and passport; willingness to travel 60-80% within your region
Global clinical trial experience
Strong understanding of regional/country culture and medical practices

Benefits

Comp & perks

Competitive compensation
Comprehensive benefits
Opportunity to work on meaningful clinical research that advances global healthcare