Clinical Study Co-ordinator - Real World Evidence

UK-based Clinical Research Co-ordinator (Real World Evidence) (Home based, United Kingdom)

You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

The Study Co-Ordinator will be assigned a portfolio of both US and Global Real World Evidence studies to carry out the following tasks;

• Manage/Assist with PO set-up
• Schedule and Coordinate the proposal review process including Evidence Connect workflow
• Ensure compliance with data entry guidance for Evidence Connect.
• Ensure completeness of documentation in Evidence Connect to enable teams to make effective business decisions
• Manage Evidence Review Team (ERT) Proposal review process including scheduling meetings, taking minutes, and managing document upload/storage for compliance purposes
• Special projects as assigned to support the Data & Analytics Team
• Assist the tumor teams and contribute towards start-up, execution, close out and reporting  of real world evidence studies
• Lead the coordination of administrative tasks and provide operational support during study process, governance, audits and regulatory inspections, according to company policies, SOPs and regulations

Of particular interest are candidates with experience working in a laboratory environment within commercial clinical research in the UK. 

Those with strong project management skills who are able to confidently communicate with internal and external stakeholders would be ideal.

Additional detail;

• Bachelor’s degree or equivalent industry-relevant experience
• Knowledge of regulatory authorities’ requirements on electronic submissions in several regions (eg, US, Europe, etc.)
• 2 years' experience in scientific research gained in a pharmaceutical environment
• A dedicated team player with excellent communication and influencing skills with experience working in multidisciplinary matrix teams

Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

#LI-Remote

#LI-DB1