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Monitor sponsor-dedicated clinical trials across sites in Chile for ICON, a global healthcare research organization. Support protocol adherence, reliable study data, and participant safety throughout each trial.
विवरण
- Conduct site qualification, start-up, monitoring, and close-out visits for clinical trials.
- Check that trials follow protocols and protect data quality and patient safety.
- Work with investigators and site teams to support effective study conduct.
- Review study data and resolve queries to maintain reliable clinical records.
- Help prepare and review study materials, including protocols and clinical study reports.
- Design and analyse trials, interpret complex medical data, and support the development of new treatments and therapies.
आवश्यकताएँ
- Hold a bachelor’s degree in a scientific or healthcare-related discipline.
- Have at least two years of experience as a Clinical Research Associate.
- Bring thorough knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Demonstrate strong organization, communication, and attention to detail.
- Work effectively both independently and with others in a fast-paced setting.
- Be willing to travel as needed, approximately 60%.
- Have the legal right to work in Chile.
लाभ
- Competitive base pay with performance-based incentives.
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life insurance and disability coverage.
- Employee assistance programs and wellbeing resources.
- Structured training and career paths with learning and development opportunities.
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