Clinical Data Analyst
About the role
This vacancy has now expired. Please see similar roles below...
- 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.
- Act as facilitator for Patient Centric Monitoring set-up, implementation and training within the cross-functional project team.
- Track the implementation of Patient Centric Monitoring within the cross-functional project team.
- Coordinate the set-up of the analysis platform, listing and working tools for Clinical Data Analysis.
- Conduct risk indicator analysis, make independent decisions on analysis outputs and communicate them to the project team.
- Support preparation, conduct and follow-up of the Quality Risk Review Meetings for effective communication with the project team and for effective resolution of study and site performance and quality issues.
- Support cross-functional ICONik users with system set-up and use.
- Act as mentor for Central Monitoring team members.
- Support internal and external promotion of Patient Centric Monitoring and related systems.
- Travel (approximately 5%) domestic and/or international.
- Other duties as assigned.
- To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Good organizational skills. Ability to manage multiple tasks and meticulous attention to detail.
- Good written and verbal communication skills.
- Good written and spoken English.
- Good Computer skills: e.g. Microsoft Word, Excel, PowerPoint, Outlook.
- US/LATAM/CAN: prior central monitoring experience or a minimum of 3 years of relevant clinical research industry experience.
- EU/APAC: prior central monitoring experience or relevant clinical research industry experience.
- Bachelor's Degree or local equivalent.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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