Job Description:
• 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 resolve queries to maintain high-quality clinical data
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports
• Take responsibility for deliverables and work collaboratively on clinical trial monitoring activities
• Design and analyse clinical trials, interpret complex medical data, and contribute to innovative treatments and therapies
Requirements:
• Bachelor's degree in a scientific or healthcare-related field
• Minimum of 2 years of experience as a Clinical Research Associate
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
• Strong organizational and communication skills, with attention to detail
• Ability to work independently and collaboratively in a fast-paced environment
• Willingness to travel as required, approximately 60%
• Legal right to work in the country where the role is based
Benefits:
• Competitive base salary
• Performance related incentives
• Medical, dental, and vision coverage where applicable
• Health and wellbeing programmes
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes
• Wellbeing resources
• Learning and development opportunities through structured training and career pathways