Clinical Study Team Assistant – Patient Recruitment

• Assist in monitoring clinical trial sites
• Ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines
• Support site management activities, including documentation preparation, data entry, and tracking site performance metrics
• Collaborate with cross-functional teams to facilitate communication and address site-related issues
• Maintain accurate records of site activities
• Contribute to the preparation of monitoring reports
• Participate in training and development initiatives to enhance knowledge and skills in clinical trial management

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research
• Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory
• Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively
• Basic knowledge of clinical trial processes and regulatory requirements is a plus
• Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment
• Legal right to work in the country where the role is based

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways