ProPharma is seeking a Freelance Senior Clinical Research Associate to support study monitoring for assigned sites, including in-person and remote visits. The role emphasizes compliance with GCP and regulatory requirements, with involvement in site initiation, feasibility, and document management.
The ideal candidate brings 5+ years of CRA experience, strong communication skills, and proficiency with EDC/CTMS/eTMF systems to ensure data integrity and study success.
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Remote Freelance SCRA (Romania) | Clinical Monitoring Pro employer: propharmagroup
ProPharma is an exceptional employer that fosters a collaborative and innovative work culture, particularly for those in the Global Life Sciences sector. With a strong focus on employee growth and development, team members benefit from flexible hybrid working arrangements that promote work-life balance while engaging in meaningful projects that impact the industry. Join us to be part of a dynamic team dedicated to excellence in talent acquisition and make a real difference in the lives of professionals across Quality & Compliance, Regulatory Sciences, and more.
