Clinical Research Associate - Sponsor Dedicated

ICON Strategic Solutions; United Kingdom; On-site; GBP 35,000 - 55,000; Full time

Job summary

Join a leading clinical research organization as a Clinical Research Associate, where you will contribute to impactful studies while traveling internationally. This role emphasizes process improvement, regulatory compliance, and data integrity. Enjoy a supportive culture that values high performance and offers competitive benefits, including health insurance and retirement plans. Be part of a diverse team that fosters inclusion and supports your professional growth. If you're passionate about clinical research and eager to make a difference, this opportunity is perfect for you.

Benefits

Health Insurance

Retirement Plans

Employee Assistance Programme

Flexible Benefits

Various Leave Entitlements

Life Assurance

Qualifications

• Previous experience as a Clinical Research Associate is preferred.
• Expert knowledge of ICON's SOPs and relevant regulations.

Responsibilities

• Recruit investigators and coordinate activities to set up studies.
• Ensure timely data entry and maintain study documentation.
• Participate in study closeout and documentation review.

Skills

Clinical Research Experience

Knowledge of ICH and GCP

Data Entry Skills

Regulatory Submission Knowledge

Communication Skills

Education

Bachelor's Degree in Life Sciences

Clinical Research Certification

Tools

ICON Systems

Job description

As a Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Please note that previous CRA experience is preferred.

What you will be doing:

• Recognize, exemplify, and adhere to ICON's values centered on People, Clients, and Performance.
• Contribute to process improvement initiatives to streamline workflows, add value, and meet client needs.
• Travel at least 60% of the time (international and domestic).
• Maintain expert knowledge of ICON's SOPs/WPs, ICH, GCP, and relevant regulations.
• Familiarity with ICON systems.
• Ensure timely and accurate data entry into ICON systems.
• Recruit investigators and coordinate activities to set up and monitor studies.
• Identify investigators and assist in regulatory submissions.
• Design patient information sheets and consent forms.
• Ensure timely ethics/IRB submissions and conduct monitoring visits according to SOPs.
• Maintain study documentation, motivate investigators, and complete study status reports.
• Manage drug storage and accountability as per SOPs.
• Keep the Project Manager informed and process case record forms to quality standards.
• Participate in study closeout and documentation review.
• Maintain confidentiality and assume additional responsibilities as directed.
• Ensure proper storage, handling, and documentation of Investigational Products (IPs).
• Participate in data reviews, training, mentoring, and marketing efforts as appropriate.
• Perform other duties as assigned.

What ICON can offer you:

• A diverse culture that rewards high performance and nurtures talent.
• Competitive salary and benefits focused on well-being and work-life balance.
• Benefits include various leave entitlements, health insurance, retirement plans, Employee Assistance Programme, life assurance, and flexible benefits.
• Visit our careers website for more information: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental. We are committed to providing an accessible environment and equal opportunity for all applicants. For accommodations, please contact us through: https://careers.iconplc.com/reasonable-accommodations

We encourage you to apply even if you do not meet all the requirements, as you may still be a great fit for this or other roles at ICON.