Clinical Study Manager

• Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines
• Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies
• Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans
• Lead the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies
• Ensure data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle
• Design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies
• Coordinate clinical trial management delivery, resolve issues, and develop team capability

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements
• Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively
• Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners
• Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials
• 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