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Clinical Data Analyst

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About the role

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Clinical Data Analyst
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.  The Clinical Data Analyst is responsible for Central Monitoring conduct on projects and for support to Patient Centric Monitoring process implementation within ICON.
 
Overview of the Role
  • 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.
Role Requirements
  • 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.
  • Bachelor's Degree or local equivalent.
Benefits of Working in ICON
 
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package.  This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
 
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.   
 
What’s Next?
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
 
 
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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