Senior Clinical Research Professional
2 weeks ago
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization.
We foster an inclusive environment driving innovation and excellence, where our diverse team members collaborate to shape the future of clinical development.
We are currently seeking an experienced Senior CRA/Clinical Research Associate II to join our dynamic team.
Your Role
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- E nsure 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 the preparation and review of study documentation, including protocols and clinical study reports.
About You
- 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.
What We Offer
- Our competitive salary is £55,000 - £70,000 per annum.
- A range of annual leave entitlements.
- Various health insurance offerings to suit you and your family's needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- A Global Employee Assistance Programme, Life Works, offering 24-hour access to a global network of specialized professionals.
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and more.
About Us
We are committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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