Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolution of queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• A minimum of 2 years of experience as a Clinical Research Associate or in a similar role.
• Strong understanding of clinical trial processes and regulatory requirements.
• Excellent communication and interpersonal skills to work effectively with diverse teams.
• Ability to manage multiple projects and priorities in a fast-paced environment.

Benefits

• Competitive salary and benefits package.
• Flexible working hours with the ability to work remotely.
• Opportunities for professional development and career advancement.
• A collaborative and inclusive company culture.
• Access to cutting-edge technologies and resources in clinical research.