At a Glance
- Tasks: Lead clinical risk assessments and manage documentation for trial protocols.
- Company: Join ICON, a leader in the pharmaceutical industry with a focus on innovation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and annual leave.
- Other info: Work remotely and lead cross-functional teams in a dynamic environment.
- Why this job: Make a real impact by improving risk management strategies in clinical trials.
- Qualifications: Bachelor’s degree in a health-related field and 6+ years of industry experience.
The predicted salary is between 60000 - 80000 £ per year.
ICON is looking for a Clinical Risk Surveillance Lead to facilitate trial protocol risk assessments and manage related documentation. Candidates must have a Bachelor’s degree in a health-related field and at least 6 years of experience in the pharmaceutical industry. The role offers the opportunity to work remotely while leading cross-functional teams to improve risk management strategies.
ICON provides competitive salaries, annual leave entitlements, health insurance, and flexible benefits.
Remote Clinical Risk Surveillance Lead (RBQM & Analytics) employer: ICON
ICON is an exceptional employer that prioritises employee well-being and professional growth, offering a flexible remote work environment for the Clinical Risk Surveillance Lead role. With competitive salaries, comprehensive health insurance, and generous annual leave, ICON fosters a supportive culture that encourages collaboration and innovation, making it an ideal place for those seeking meaningful and rewarding careers in the pharmaceutical industry.
