About the company This employer is a multinational company specializing in clinical research and trial management services for the healthcare sector. Their comprehensive research solutions support medical advancement initiatives across multiple therapeutic areas and they have established themselves as a trusted and respected partner within the global healthcare research community. About the job In this position, you will be providing clinical oversight, site management and regulatory support services related to medical research studies. This role also involves contribution to data quality assurance activities in collaboration with clinical operations and sponsor teams. Job Responsibilities: Provide site support through consultation on study protocol and regulatory matters Handle monitoring activities along with data verification at clinical research sites Work collaboratively with clinical teams on study implementation and compliance activities, offering guidance and assistance as necessary Develop monitoring reports and documentation as required for regulatory submissions Contribute to operational excellence by implementing best practices and driving quality improvements Job Requirements: Bachelor&aposs Degree in Life Sciences, Nursing, Medicine or other healthcare-related fields Minimum of 1 year working experience in clinical research or healthcare industry Ability to work independently and manage multiple study sites Excellent analytical, communication and problem-solving skills Extensive travel required to clinical research sites across assigned regions What's on offer: Exciting career progression opportunities in a leading industry player Competitive remuneration and benefits The chance to be part of a growing industry that makes a difference in people's lives Show more Show less