CRA II

In this role, you contribute to the design, analysis, and oversight of clinical trials to support faster access to innovative therapies. You will perform monitoring activities, ensure patient safety, data integrity, and protocol compliance within a collaborative team. You’ll work with investigators and site staff to keep studies on track and deliver high-quality study documentation. This position offers the chance to impact patient care at a global, value-driven organization with opportunities for professional growth.

• 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

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data
• Contribute to preparation and review of study documentation, including protocols and clinical study reports

• Bachelor's degree in a scientific or healthcare-related field
• Minimum of 2 years of experience as a Clinical Research Associate
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
• Strong organizational and communication skills, with attention to detail
• Ability to work independently and collaboratively in a fast-paced environment
• Willingness to travel approximately 60%

• Strong communication skills
• Attention to detail
• Ability to work both independently and in a team
• Collaborative mindset in fast-paced environments
• ICH-GCP guidelines
• Clinical trial processes knowledge