Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate, with a minimum of 2 years experience in solid tumors (ideally NSCLC, prostrate and/or breast, melanoma)
A phase 1 oncology studies experience would be an advantage
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Willingness to travel as required (approximately 60%)

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

Senior Clinical Research Associate

Key skills