Career Opportunities with ECN Operating LLC

A great place to work.

 
Careers At ECN Operating LLC
Share with friends or Subscribe!

Are you ready for new challenges and new opportunities?

Join our team!

Current job opportunities are posted here as they become available.

Subscribe to our RSS feeds to receive instant updates as new positions become available.

 

 

 

Clinical Research Source/CTMS Specialist

Department: Finance
Location:

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

 

 

 

 

Applicant Tracking System Powered by ClearCompany HRM Applicant Tracking System