Sr. Clinical Trial Manager, FSP

📋 Description

• Oversee all clinical operational and quality activities for assigned clinical studies of moderate
• Take on additional leadership responsibilities when required, including regional Clinical Trial
• Develop and maintain clinical study tools and documentation, including Monitoring Plans, Monitoring
• Contribute to the development and execution of Master Action Plans and ensure the timely
• Participate in the development and review of Case Report Forms (CRFs), CRF guidelines, informed
• Collaborate with project managers to prepare and participate in client meetings, including bid

🎯 Requirements

• Bachelor's degree or equivalent academic or vocational qualification in a relevant discipline, such
• At least 8 years of relevant professional experience in clinical research, clinical trial
• Equivalent combinations of education, professional training, and directly related experience may
• Comprehensive knowledge of clinical monitoring practices, clinical trial operations, and study
• Strong understanding of international clinical research regulations and guidelines, particularly
• Proven leadership capabilities, including experience mentoring, training, motivating, and

🎁 Benefits

• Work arrangement: Fully remote position based in Brazil.
• Employment type: Full-time opportunity.
• Work schedule: Standard working hours, Monday to Friday.
• Global exposure: Opportunity to collaborate with international clinical research teams and
• Professional development: Exposure to complex clinical studies, advanced research processes, and
• Meaningful impact: Opportunity to contribute to scientific innovation and clinical research