Overview
In this role you oversee clinical trial monitoring to ensure protocol compliance, regulatory alignment, and GCP standards. You’ll lead site visits, drive data quality, and collaborate with cross-functional teams to support trial execution. You’ll train and guide site staff, nurture strong site relationships, and contribute to continuous improvement. This is a sponsor-dedicated position with a global partner network, offering opportunities to shape trial conduct at scale.
Pay / Benefits
- Competitive base salary
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities
Responsibilities
- Monitor sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, resolve issues, and support trial success
- Collaborate with cross-functional teams to ensure timely, accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs to maintain high conduct standards
- Build and maintain relationships with site personnel and stakeholders to enable smooth trial operations
Key requirements
- Bachelor degree in a relevant scientific or healthcare field
- Extensive experience as a Clinical Research Associate with strong regulatory and trial process understanding
- Proven ability to manage multiple sites and projects simultaneously with strong organizational skills
- Expertise in monitoring practices, data integrity, and site management; proficient with clinical trial software/tools
- Excellent communication, interpersonal, and stakeholder management skills; ability to influence in complex environments
- Willingness to travel approximately 60%
- communication
- stakeholder management
- problem-solving
- clinical trial monitoring
- GCP compliance
- data integrity
CRA II/Sr CRA - Sponsor Dedicated in Swansea employer: Icon Clinical PLC
At ICON, we pride ourselves on being a values-driven organisation that fosters a collaborative and inclusive work culture. As an Operation Program Specialist, you will not only contribute to meaningful healthcare projects but also benefit from our comprehensive rewards package, including competitive salaries, health programmes, and robust career development opportunities. Join us in Sofia, Warsaw, or Swansea, where your expertise will be valued and your professional growth supported in a dynamic environment dedicated to bringing new treatments to patients faster.
