CRA II

ICON plc; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in the UK is seeking a Clinical Research Associate II to oversee clinical trials. The ideal candidate will have experience in monitoring trials, ensuring compliance, and collaborating with site staff. This role offers a competitive salary and comprehensive benefits including health insurance and retirement planning. Candidates must be willing to travel and possess a valid driver's license.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of ICH-GCP guidelines.
• Ability to travel at least 60% of the time.

Responsibilities

• Conduct site visits for clinical trials.
• Ensure data integrity and patient safety.
• Collaborate with investigators for study conduct.

Skills

Clinical trial processes

Strong organizational skills

Communication skills

Attention to detail

Ability to work independently

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

CRA II page is loaded## CRA IIremote type: Remotelocations: UK, Readingtime type: Full timeposted on: Posted Todayjob requisition id: JR139610Clinical Research Associate - Oncology - UK StudiesICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.**What you will be doing*** Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.* Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.* Collaborating with investigators and site staff to facilitate smooth study conduct.* Performing data review and resolution of queries to maintain high-quality clinical data.* Contributing to the preparation and review of study documentation, including protocols and clinical study reports**Your profile*** 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.* Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license**What ICON can offer you:**Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:* Various annual leave entitlements* A range of 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.* Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.* Life assurance* Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.Visit our to read more about the benefits ICON offers.At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is 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.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request.to apply###