
Clinical Research Manager
Posted Aug 24

Posted Aug 24
This is a fully remote position, open to applicants in Turkey.
• Supervise clinical monitoring activities and the performance of the CRA team to ensure compliance with ICH-GCP, local regulations, and company SOPs.
• Allocate resources for CRAs and evaluate workloads to achieve study deliverables.
• Ensure that CRAs possess the necessary knowledge and skills to conduct monitoring activities with a high degree of quality.
• Manage CRA performance and monitor quality indicators.
• Enhance relationships with sites and assist in trial execution.
• Evaluate monitoring quality, address compliance issues, and support study and site milestones.
• Conduct assessment visits and accompany visits as needed.
• Contribute to process improvements and manage risk identification and resolution.
• Assist with site audits, inspections, and Site Compliance Visits, including corrective actions and follow-ups.
• Review and authorize CRA-related expenses while identifying opportunities for cost savings.
• Recruit, hire, onboard, assign tasks, support, evaluate, mentor, and develop team members.
• Tackle personnel issues and promote career development.
• Foster communication, collaboration, and a positive team culture.
• Bachelor’s degree or higher in a scientific or healthcare field; advanced degrees are preferred.
• Proficient in Microsoft Word, Excel, PowerPoint, and Outlook.
• Fluent in both written and spoken English.
• At least 5 years of industry experience in the pharmaceutical or CRO sectors, or a relevant field.
• A minimum of 2 years of experience in people management or project management within progressive clinical research is preferred.
• Comprehensive understanding of the drug development process, including expert knowledge of international standards (ICH GCP) and health authority requirements.
• Understanding of all aspects of monitoring and trial execution; prior CRA experience is preferred.
• Exceptional interpersonal, organizational, written, and verbal communication skills.
• Proven experience in team leadership.
• Experience in oncology is highly recommended.
• Willingness to travel as needed for business purposes.
• Valid driver’s license in applicable countries.
• Competitive salary and performance-based bonuses.
• Opportunities for professional development and growth.
• Comprehensive health and wellness benefits.
• Flexible work environment and schedule.
• Supportive team culture and collaborative atmosphere.
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Emerald Clinical
Everest Clinical Research
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