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Data and Documentation Specialist

ICON Public Limited Corporation

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...

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.

Data and Documentation Specialist- This position is responsible for the receipt and distribution of incoming in-home clinical trial documentation to appropriate personnel as well as maintenance of the homecare worksheet email box. Responsible for coordination of queries with internal teams; coordinating finalization of all documentation from clinical service providers on a timely basis. Responsibilities also include the filing of approved homecare worksheets in the Central Study File.

This position is also responsible for Sponsor reports including the creation and distribution of the reports to the study managers per the requested frequency.

ESSENTIAL DUTIES AND RESPONSIBILITIES

The incumbent will perform other duties as assigned.Proactive communication with clinical study managers Review and monitor secure email and eFax for documentation to distribute to appropriate departments and to respond as required.Maintain Documents and Files, in accordance with GCP and study specific requirements and ensure Central Study File is updated in a timely manner and updated as necessaryCreate metrics and distribute to clinical study managers at specified intervalsAssist with internal audits, and study close out activities

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.

Job posted: 2021-01-28

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