CDM Freelance Solutions
Based in Europe · Supporting U.S. & EU Sponsors

Freelance Clinical Data Management Services for Sponsors & CROs

End-to-end and à la carte data management support for clinical trials — flexible, compliant, and cost-efficient.

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6+ Years Experience

Phase I–III clinical trials across multiple therapeutic areas

ICH-GCP · CDISC · SDTM

Strong regulatory and data standards expertise

Flexible Engagement

Project-based, part-time, or full-time contractor models

EU-Based, US-Ready

Cost-efficient support across time zones

Services

Data Management Services

Choose the level of support that fits your study — from full-service management to targeted expertise.

Full-Service Clinical Data Management Package

A complete, end-to-end clinical data management solution covering every aspect from study start-up to database lock and regulatory submission.

  • Study protocol and document review
  • CRF design and annotation
  • EDC system setup and configuration
  • Data Management Plan (DMP) creation
  • Site staff training on EDC and data quality
  • Ongoing data cleaning, validation, and discrepancy management
  • Data reconciliation with external sources (labs, imaging, wearables)
  • Patient tracking and missing data reporting
  • Implementation of data standards (CDISC, SDTM)
  • Vendor data integration
  • Preparation for regulatory submission

Best for

Sponsors or CROs seeking a single point of contact for all data management needs, ensuring seamless, compliant, and high-quality data throughout the trial.

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Most Popular

Core Data Management Package

A streamlined package focused on the most critical data management activities for trials with limited complexity or budget.

  • Protocol and CRF review
  • EDC setup and basic configuration
  • DMP creation
  • Data cleaning and validation
  • Discrepancy management
  • Patient tracker and missing data reports

Best for

Smaller sponsors, investigator-initiated studies, or organizations with in-house capabilities for some services but needing expert support for core data management functions.

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Custom / À la Carte Data Management Services

A flexible, modular offering where clients choose only the services they need.

  • CRF design and annotation
  • EDC setup or migration
  • Site staff training
  • Data reconciliation
  • Data standards implementation
  • Vendor data integration

Best for

Clients with specific gaps in their data management process or those looking to supplement their existing team with targeted expertise.

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Process

How It Works

  1. 1

    Initial Consultation

    Discuss your study needs and scope

  2. 2

    Proposal & Scope

    Receive a tailored proposal and timeline

  3. 3

    Onboarding

    Fast, structured kickoff and access setup

  4. 4

    Ongoing Support

    Reliable delivery through to database lock

Why me

Why Work With Me

Over 6 years of experience managing Phase I, II, and III clinical trials across multiple therapeutic areas. Strong knowledge of ICH-GCP, CDISC, SDTM, and regulatory requirements. Flexible and cost-effective service models tailored to your needs. Commitment to delivering high-quality, compliant, and timely results.

Phase I–IIIICH-GCPCDISC / SDTMEDC systems
  • Open to different collaboration models — from project-based support to full-time contractor arrangements
  • Based in Europe, seamlessly supporting U.S.-based companies
  • Cost-efficient and reliable service without compromising quality
  • Direct, single point of contact throughout the engagement

FAQ

Frequently Asked Questions

Let's Talk About Your Study

Get a free consultation and a tailored proposal within 48 hours.

Book a Free Consultation

Proposal within 48 hours

Direct, single point of contact

NDA signed before project details