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About the role
Key responsibilities & impact- Support the management of clinical trial sites by assisting with site monitoring activities
- Ensure compliance with study protocols and maintain high standards of operational efficiency
- Assist in monitoring clinical trial sites for 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 and contribute to monitoring reports
- Participate in training and development initiatives
Requirements
What you’ll need- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research
- Experience working on global position
- 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
- Willingness to travel as required (approximately 25%)
- Legal right to work in the country where the role is based
Benefits
Comp & perks- 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