Clinical Research Coordinator

Clinical Research Coordinator

Location: Northwood, North London

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Summary:

This position is responsible for timely completion of paper based or electronic case report forms, completing or facilitating the completion of all sponsor produced queries, performing quality control checks of case report forms prior to sponsor review and is the primary liaison for the Clinical Research Associate (CRA) during monitoring visits.

Responsibilities:

• Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Travel: Travel to other sites within the network may be required to support increases in workload and, or studies/projects as needed.
• Represents data management at all internal and external meetings and providing data management updates as required.
• Performs additional quality control checks prior to case report form completion.
• Oversee CRA monitoring visit and complete or facilitate the completion of queries generated from visit.
• Complete closure forms and packaging of source documents and case report forms at the end of assigned study.
• Review and perform quality checks on subjects research chart for completion of case report forms.
• Participate in internal and external audits as required.
• Follow any reasonable directive from the Medical Director, PI and Clinical Data Services Supervisor.
• To undertake other reasonable related duties as may be assigned from time to time.

Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON 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, 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 through the form below.