Clinical Data Coordinator (Office based in Scotland)

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

PLEASE NOTE, THIS ROLE IS OFFICE BASED IN SCOTLAND

What you will be doing:

• Supports activities related to development of the clinical data management systems (CDMS).
• Processes and reviews the CRF, third party data, and local laboratory data, if applicable.
• Supports and leads the clinical data review activities associated with a clinical trial.
• Prepares and completes quality control reviews and delivers the end product of clinical data that meets agreed upon data integrity standards
• Serves as lead clinical data coordinator for one or more projects.
• Reviews clinical and external data for subjects enrolled in clinical research protocols based on edit specifications / data validation programs to facilitate data review.
• Maintains Data Management Plan (including CRF related components) as appropriate.
• May be responsible for data entry activities, quality control reviews, identification and documentation of data problems during CRF tracking, Casebook
• Manager set-up and maintenance and serve as primary contact for data entry activities for functional management and internal study team members.
• Performs proficient reviews of study datasets prior to client transfer.
• Manages the data review and external data reconciliation process.
  Mentors and trains other team members in data management skills and processes for individual studies.
• Utilizes internal systems to optimize and communicate resourcing issues and needs.
• Ensures study and task metrics are tracked and communicated to the project team and functional management.
• May participate in sponsor and/or third party audits

About you:

• Bachelor’s degree or equivalent, in Health or Science discipline with experience in clinical research.
• Data Management experience.
• Experience working on a clinical trial.
• Experience working in highly diverse teams within clinical research/healthcare; cross-functional, global, multi-regional.
• Project management skills, preferred.
• Vendor management skills, preferred.
• Advanced Microsoft Office skills including the ability to manipulate and analyze data.
• Highly organized with excellent written and verbal communication.

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 maximise 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 careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

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 or submit a request here.

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.

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