Senior Clinical Research Associate

🕒 June 23

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

Healthcare Insurance • Biotechnology • Pharmaceuticals

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• 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

• 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

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