Clinical Validation Specialist at OmniComm Systems, Inc. - Job Vacancy in 2018

Clinical Validation Specialist OmniComm Systems, Inc. April 2018 . OmniComm Systems, Inc. career opportunities for those who have knowledgeable and are pursuing a job. Join OmniComm Systems, Inc. and be part of a healthy nation work to contribute to contemporary society reliably. Everyone in the OmniComm Systems, Inc. be valued in accordance with the achievements and also potential, if you are a individual who meets the desired qualifications, we look forward to inviting you to join with OmniComm Systems, Inc.. They give you career opportunities within the business, according to the profession that you could acquire. The following is in depth information about job Clinical Validation Specialist OmniComm Systems, Inc. that have been written at the first of this month.

Clinical Validation Specialist April 2018
OmniComm Systems, Inc.

Job Summary

The Clinical Validation Specialist is responsible for quality testing of electronic case report forms, custom export datasets and further electronically generated trial specific documentation in conjunction with the Project Manager and Study Designer of the project. Responsible for the accurate documentation of the test process.

Please submit CV when applying.


Strong work ethic; outstanding character while working within a team environment; excellent organization and communication skills; detail-oriented, correct, and precise working style.

Responsibilities and Duties

  • Test electronic case report forms against requirements and record test results.
  • Test custom export data-sets against client’s database specification and record test results.
  • Test study archives and record test results.
  • Document defects.
  • Execute test plans.
  • Assist in test plan development.
  • Communicate frequently with team members about test results and test status.
  • Assist in study audit preparations.

Qualifications and Skills


  • Knowledge of Electronic Data Capture ("EDC") and experience with applications designed with 21 CFR part 11 compliance.
  • Strong understanding of Quality Assurance principles, techniques and technology.
  • Experience in testing methodology and software testing a plus.
  • Clinical experience such as nurse, data manager, research associate, clinical data entry a plus.
  • Ablity to understand study protocols and requirements.
  • Working style with attention to detail and accuracy.
  • Flexible and able to work under time pressure.
  • Fluent in English (written and spoken).


  • Excellent communication skills.
  • Self-motivated with strong organizational skills.
  • Ability to work well both individually and with a team.


Not only do we provide great products but our culture is something to brag about! We believe that our employees are the most important piece of the puzzle.

  • A great Company Culture
  • Comfortable working space
  • Tuition Reimbursement Program
  • Annual Bonus Program
  • Holiday - 30 days annually

Job Type: Full-time

Salary: €30,000.00 to €34,000.00 /year

Required language:

  • English

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