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Roles and Responsibilities:
- Master remote monitoring techniques and understand electronic data capture systems.
- Engage with patients virtually and ensure data integrity and compliance remotely.
- Monitor study progress and ensure adherence to protocols, guidelines, regulations, and SOPs.
- Maintain good clinical practices throughout the trial and ensure audit readiness.
- Review data collection quality and compliance of patients to trial visits and assessments.
Requirements and Skills:
- Master’s/Bachelor’s degree in Pharma, Science, Computer Science, Information Systems, or related field.
- 3 to 8 years of experience as a Clinical Research Associate, Data Management Associate, or similar role in the CMS domain.
- Strong problem-solving skills and team spirit.
- Excellent communication skills and adaptability.
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