At a Glance
- Tasks: Oversee clinical trial activities and ensure regulatory compliance while guiding site staff.
- Company: Join ICON, a leader in clinical research with a supportive culture.
- Benefits: Enjoy competitive salaries, health insurance, retirement planning, and work-life balance support.
- Why this job: Make a real impact in clinical research and advance your career in a dynamic environment.
- Qualifications: 4+ years of CRA experience and strong organisational skills required.
The predicted salary is between 50000 - 60000 £ per year.
ICON is seeking a Senior Clinical Research Associate with expertise in clinical trial monitoring in the UK. Your role will involve overseeing trial activities, ensuring regulatory compliance, and guiding site staff. The ideal candidate has over 4 years of CRA experience, strong organizational skills, and proficiency in clinical trial processes.
ICON offers competitive salaries and a wide range of benefits including health insurance, retirement planning, and support programs to ensure work-life balance.
Senior CRA - Lead Clinical Monitoring (UK) in Reading employer: ICON
ICON is an exceptional employer that prioritises the well-being and professional growth of its employees. With a strong commitment to work-life balance, competitive salaries, and comprehensive benefits including health insurance and retirement planning, ICON fosters a supportive work culture where Senior Clinical Research Associates can thrive in their careers while making a meaningful impact in clinical research.
