Project Support Coordinator - Cdm

Thermo Fisher Scientific UK

Standard office job (mon-fri)
Clinical data management project support
Electronic trial master file (etmf) filing
User acceptance testing data generation
Thermo Fisher Scientific is seeking a Project Support Coordinator to assist Clinical Data Management (CDM) teams with various administrative tasks. The ideal candidate should have a relevant educational background and strong organizational skills, with an emphasis on attention to detail and the ability to manage multiple tasks effectively

Job Summary

  • You will provide administrative support to Clinical Data Management project teams to help enable customers to make the world healthier, cleaner, and safer.
  • The role involves performing various tasks including generating test data for user acceptance testing, maintaining patient trackers, and filing documents in the eTMF.
  • Candidates must demonstrate strong organizational skills and the ability to analyze project-specific data to ensure accuracy while working within ICH Good Clinical Practices.

Matching Summary

Match Score: 85

Thermo Fisher Scientific is seeking a Project Support Coordinator to assist Clinical Data Management (CDM) teams with various administrative tasks. The ideal candidate should have a relevant educational background and strong organizational skills, with an emphasis on attention to detail and the ability to manage multiple tasks effectively.

Skills & Requirements

Must-have

  • Clinical Data Management project support
  • Electronic Trial Master File (eTMF) filing
  • User acceptance testing data generation
  • Medidata EOS site creation
  • Patient tracker maintenance
  • Study-specific metrics reporting

Nice-to-have

  • Strong attention to detail
  • Ability to work independently
  • Good organizational skills
  • Effective oral communication
  • Self-motivated positive attitude

Key Requirements

  • Bachelor's degree preferred in Pharmacy, Nursing, Biology or related field
  • 0 to 4 years of comparable experience
  • Proficiency in MS Office (Word, Excel, PowerPoint)
  • Knowledge of Country Regulations and ICH Good Clinical Practices

Work Rights

Not specified

Tailored Resume

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