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Clinical Data Manager - Mid-Level (Remote)

Penfield Search Partners

Fairfield, CT(remote)

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JOB DETAILS
SKILLS
Acceptance Testing, Biostatistics, Biotech and Pharmaceutical, Case Report Form (CRF), Clinical Data Collection, Clinical Data Interchange Standards Consortium (CDISC), Clinical Data Management, Clinical Support, Contract Research Organization (CRO), Cross-Functional, Data Cleaning, Data Management, Data Quality, Data Structures, Detail Oriented, Drug Development, Electronic Data Capture (EDC), Industry Standards, Maintain Compliance, Medical Dictionary for Regulatory Activities (MedDRA), Oracle, Phase II Clinical Trials, Phase III Clinical Trials, Process Improvement, Regulatory Compliance, Regulatory Requirements, Startup, Team Player, Time Management, World Health Organization Drug Reference List (WHODrug)
LOCATION
Fairfield, CT
POSTED
1 day ago

Contact: Neisha Camacho/Terra Parsons -

teamnt@penfieldsearch.com


No 3rd party candidates

We are partnering with a growing biotech organization seeking a Clinical Data Manager to support ongoing and upcoming clinical programs across multiple Programs

This role will sit within a cross-functional clinical development team and support end-to-end data management activities, with a strong focus on execution, quality, and collaboration. The ideal candidate brings solid hands-on data management experience, with exposure to Phase II & III trials in a fast-paced biotech environment.

Key Responsibilities

  • Support clinical data management activities across studies from start-up through database lock
  • Partner with CROs and vendors to ensure high-quality, timely data delivery
  • Collaborate cross-functionally with Clinical, Biostatistics, Programming, and Medical teams on data collection and review strategies
  • Contribute to development and review of key deliverables, including:
    • Data Management Plans (DMPs)
    • eCRF design and completion guidelines
    • Edit checks and query logic
    • User Acceptance Testing (UAT)
    • Data review and cleaning processes
  • Perform ongoing data review and support query management to ensure data quality and consistency
  • Support implementation of data standards and process improvements
  • Assist with inspection readiness and ensure compliance with regulatory requirements and industry standards

Qualifications

  • BS in a scientific or clinical discipline
  • ~5–8 years of clinical data management experience within biotech, pharma, or CRO environments
  • Hands-on experience with EDC systems (e.g., Medidata Rave, Oracle, Veeva)
  • Working knowledge of CDISC standards (SDTM/ADaM) and downstream data usage
  • Experience supporting Phase II or III clinical trials; CNS experience is a plus
  • Exposure to CRO/vendor oversight
  • Understanding of data structures and dictionaries (e.g., MedDRA, WHODrug)
  • Strong collaboration skills and ability to work cross-functionally
  • Detail-oriented, proactive, and comfortable in a dynamic environment

About the Company

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Penfield Search Partners