Clinical Research Professional
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Experienced Clinical Research Associate (CRA) with 13+ years of monitoring and site management experience in oncology, rare diseases, and multi-therapeutic clinical trials. Skilled in remote and onsite monitoring, ensuring compliance with ICH-GCP guidelines, protocol adherence, and regulatory requirements. Proven ability to manage investigational sites, verify data integrity, and drive subject enrollment.
Strong background in risk management, site evaluation, and audits. Adept at providing training to junior team members and ensuring investigational product (IP) accountability. Available for 75% travel and relocation.
Results-driven Senior Clinical Research Professional with 13+ years of experience in clinical trial management, site monitoring, and regulatory compliance. Proven ability to successfully manage global trials across diverse therapeutic areas, including Oncology, Cardiology, and Rare Diseases. Adept at ensuring ICH-GCP and regulatory compliance, with a strong focus on quality and timely execution.
Experienced in working with sponsors and investigators in a fast paced environment. Seeking to leverage extensive monitoring experience to contribute to Everest Clinical Research's commitment to excellence as a Senior Clinical Research Associate.
