Clinical Associate

• Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards
• Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits
• Collaborate with Clinical Operations, Data Management, and Biometrics
• Maintain comprehensive study documentation and records in compliance with regulations and standard operating procedures
• Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry
• Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively
• Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance
• Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites
• Willingness to travel as required (approximately 60%)
• 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