Jobs · Information Technology

Clinical Research Source/CTMS Specialist

Elite Clinical Network · United States · 2 wk ago
RemoteRemoteInformation Technology$55k–$60k/yrFull-time

Position Summary

The Clinical Research Source/CTMS Specialist is responsible for the development, standardization, and integration of clinical research source documentation. This role ensures high-quality, compliant source documentation across the research network while supporting system optimization, regulatory readiness, and operational efficiencies. The Specialist serves as a key liaison between Clinical Operations, sites, and the CTMS team to ensure seamless alignment between protocol requirements, source documentation, and system data capture standards.

Key Responsibilities

  • Source Development: Design and build standardized source document templates that align with the protocol requirements and CTMS data fields.
  • System Integration: Ensure that as CTMS templates are built, corresponding source documents are simultaneously developed to prevent data silos or compliance gaps.
  • Quality & Compliance: Directly address and mitigate audit findings related to source management by implementing network-wide standards.
  • Site Support: Act as primary point of contact for sites regarding source management issues and technical troubleshooting across the network.
  • Collaboration: Work closely with the CTMS team and Clinical Operations to ensure all templates reflect the most current regulatory and study-specific requirements.

Required Qualifications

  • Experience: 3-5 years in clinical research, specifically focused on CTMS administration, data management, or clinical site monitoring.
  • Technical Skills/Systems Experience: Proficiency in CTMS platforms and electronic source (eSource) software. Experience in template design or database logic is highly preferred.
  • Regulatory Knowledge: Deep understanding of GCP, ICH guidelines, and FDA requirements regarding source documentation and ALCOA+ principles.
  • Attention to Detail: Proven ability to translate complex clinical protocols into user-friendly, compliant site documentation.

Preferred Qualifications

  • Licenses/Certifications: CCRC, CRA, CP, or similar preferred but not required.

Core Competencies / Skills

  • Communication
  • Problem-Solving
  • Leadership
  • Strong written and verbal communication with a focus on clarity, accuracy, and professionalism

Pay

$55,000 - $60,000 annually

Schedule

N/A

Benefits

N/A

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