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Associate Data Manager (CDM) Job at Premier Research

Associate Data Manager – Fixed-Term Contract

Premier Research is seeking an experienced Associate Data Manager for a 4-month fixed-term contract. In this remote role, you will play a crucial part in ensuring the quality and integrity of clinical trial data, working with leading biotech, medtech, and specialty pharmaceutical companies. This is an excellent opportunity to enhance your clinical data management skills and contribute to the development of life-changing therapies.

Job Summary

The Associate Data Manager is responsible for supporting the preparation of clean and accurate clinical trial databases. This involves reviewing data in EDC systems, generating and resolving queries, assisting in CRF design, and participating in user acceptance testing. The ideal candidate possesses a strong understanding of clinical data management principles and experience with EDC platforms like Medidata Rave, Oracle Inform, and DataLabs.

Responsibilities

  • Review clinical trial data in CDMS/EDC systems to support the preparation of clean databases.
  • Ensure data accuracy and consistency according to the study protocol, Data Management Plan (DMP), and edit check rules.
  • Generate and resolve queries with clinical sites, vendors, Clinical Research Associates (CRAs), and client teams.
  • Review query responses, resolve data discrepancies, and update databases accordingly.
  • Assist in the design of Case Report Forms (CRFs) and the development of edit check specifications.
  • Participate in User Acceptance Testing (UAT) for CRFs, edit checks, and study-specific listings.
  • Maintain thorough documentation of testing processes, system updates, and data management activities.

Requirements

  • Bachelor’s degree in life sciences, pharmacy, health sciences, or a related technical field.
  • 3–5 years of hands-on experience in clinical data management.
  • Strong working knowledge of EDC platforms, including:
    • Medidata Rave
    • Oracle Inform
    • DataLabs
    • RDC
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
  • Strong analytical, organizational, and multitasking abilities.
  • Excellent verbal and written English communication skills.

Benefits

  • Opportunity to work on global, innovative clinical development programs.
  • Make a meaningful contribution to the development of life-changing therapies and medical technologies.
  • Enjoy a collaborative, flexible, and remote working environment.
  • Deepen your technical expertise in clinical data validation, query management, and EDC systems.
  • Competitive compensation package.

How to Apply

Interested and qualified candidates are encouraged to apply. Please submit your resume and cover letter outlining your relevant experience and qualifications. We look forward to receiving your application!