Sr Clinical Data Analyst Medical Device

Fortrea

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profile Job Location:

Bucharest - Romania

profile Monthly Salary: Not Disclosed
Posted on: 2 days ago
Vacancies: 1 Vacancy

Job Summary

Fortrea is looking for a Sr Clinical Data Analyst (24 years experience) to join our medical device team

As a Sr Clinical Data Analyst at Fortrea you will play a key role in ensuring the quality integrity and timeliness of clinical trial data across assigned studies. Working alongside a diverse group of research professionals you will collaborate closely with cross-functional project teams to support database set-up ongoing data review and database lockalways aligned with protocol requirements global harmonized SOPs and applicable GCP standards.

Your Responsibilities:

  • Ensure all allocated projects are delivered in strict accordance with protocols global harmonized SOPs and applicable GCP standards.
  • Perform clinical data management activities including data review and query management ensuring quality standards (internal and client) are met within agreed timelines.
  • Generate resolve and track queries arising from aggregate data review activities.
  • Run and execute additional programs and outputs (e.g. special listings reconciliation discrepancy listings and other outputs supporting data review).
  • Partner with study team members to support set-up maintenance and close-out of Data Management project activities; attend meetings as required.
  • Assist withor createdummy data to test edit checks database screen design/functionality and SAS reports/data listings.
  • Support the team by preparing study forms/memos and completing data management documentation and administrative activities including eTMF maintenance when required.
  • Generate study status reports and perform database extracts.
  • Assist with Database Lock activities and contribute to inspection/audit readiness.

Your experience and qualifications:

  • University/college degree in life sciences health sciences information technology or a related discipline (or a certification in allied health professions from an accredited institution).
  • Fluent in English written and spoken.
  • 2 to 4 years of applicable experience in clinical research (Data Management preferred); additional relevant experience may substitute for education requirements.
  • Hands-on experience with clinical EDC platforms.
  • Knowledge of medical terminology.
  • Strong time management skills with the ability to work to productivity metrics and timelines.
  • Solid understanding of effective clinical data management practices.

What you can expect from us:

  • Pioneering Research: Join a global CRO supporting clinical trials across multiple therapeutic areas.
  • Career Growth: Expand your skill set in a supportive environment with opportunities for development and progression.
  • Impactful Work: Help deliver high-quality data that supports the development of life-changing therapies and treatments.
  • Competitive Compensation: A competitive salary package comprehensive benefits and a rewarding bonus structure.
  • Life-Style: Flexibility to work remotely (role/location dependent) supporting a healthy work-life balance.

You can be 100% home-based in any of the EMEA locations listed on this ad.

Fortrea is a leading global clinical research organization (CRO) with decades of experience and a global footprintworking to help move clinical trials forward and make delivery easier for sponsors sites and patients.
For more information about Fortrea visit .

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race religion color national origin gender (including pregnancy or other medical conditions/needs) family or parental status marital civil union or domestic partnership status sexual orientation gender identity gender expression personal appearance age veteran status disability genetic information or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data please see our Privacy Statement.

If as a result of a disability you require a reasonable accommodation to complete your job application pre-employment testing job interview or to otherwise participate in the hiring process please fill the Applicant Accommodation Request Form. Please note that this form is only for job seekers requesting an accommodation. Do not use this form to check the status of your application.

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Learn more about our EEO & Accommodations request here.


Required Experience:

Senior IC

Fortrea is looking for a Sr Clinical Data Analyst (24 years experience) to join our medical device teamAs a Sr Clinical Data Analyst at Fortrea you will play a key role in ensuring the quality integrity and timeliness of clinical trial data across assigned studies. Working alongside a diverse group ...
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