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Based in Dnipro & Chernivtsi, Ukraine

Vitaliy Levchuk

Senior clinical research and operations professional with quality, site management, and humanitarian/forensic program experience

I support clinical and humanitarian programs with structured delivery, GCP-aligned quality practices, and cross-functional coordination. Experienced across site oversight, regulatory documentation, project timelines, and international collaboration to ensure compliant, reliable outcomes.

Contact View Experience

Quick profile

Clinical research, quality compliance, and program operations delivery

Core strengths
Clinical Research · GCP Compliance · Site Management
Operations focus
Regulatory Docs · Quality Control · Project Delivery
Certifications
Using Artificial Intelligence · Open Arguments · IELTS 6.5

Detailed experience and credentials are presented below in the profile sections.

Bio

Professional summary

Vitaliy Levchuk is a clinical research and operations professional based in Ukraine, bringing cross-functional experience spanning humanitarian work, clinical trials, quality management, regulatory compliance, and project coordination. His profile reflects structured delivery, careful documentation, and stakeholder alignment across complex initiatives.

His background also includes translation services, IT support, website design, trading, and logistics, giving him a broad operational lens and the ability to bridge technical, administrative, and client-facing needs.

Fluent in English at a full professional level, Vitaliy supports international collaboration with clear communication and reliable execution. He maintains a practical, detail-oriented approach suited to regulated and mission-critical environments.

Specialties & skills

Recruiter-ready focus areas, organized for quick review

A concise, verified view of Vitaliy’s professional capabilities based strictly on provided information, grouped for easy scanning.

Open to relevant opportunities

Clinical Research

Core specialty

  • Clinical research
  • Study monitoring
  • Site management
  • Source data verification
  • Investigational product accountability
  • Regulatory submissions

Quality & Compliance

Governance focus

  • Quality control
  • Internal auditing
  • GCP compliance
  • Regulatory affairs

Operations & Project Delivery

Execution strength

  • Project management
  • Logistics
  • Translation services

Entrepreneurial / Technical Services

Broader capabilities

  • IT desktop support
  • Website design
  • Power equipment trading
Secondary mention: venture capital exposure Location: Dnipro & Chernivtsi, Ukraine

Experience

Professional timeline

A reverse-chronological view of roles and responsibilities, presented for quick recruiter scanning. Each entry can be edited for additional achievements, metrics, and team context.

Snapshot focus

  • • Lead with role scope, program ownership, and compliance impact.
  • • Add quantified outcomes where available.
  • • Keep bullets concise for fast reading.
  1. 01

    Forensic Programme Assistant

    International Committee of the Red Cross (ICRC) • Ukraine

    April 2023 – July 2025
    • • Supported forensic program operations and cross-functional coordination.
    • • Contributed to humanitarian initiatives across multiple locations.
    • • Assisted with forensic investigations and documentation workflows.
  2. 02

    Clinical Research Specialist (Contract)

    Tigermed • Kyiv, Ukraine

    October 2021 – April 2023
    • • Worked on the 2021L001 Vaccine Study as Research Associate (0.5 FTE).
    • • Served as Quality Manager (0.25 FTE) ensuring protocol compliance.
    • • Maintained clinical trial quality standards and documentation.
  3. 03

    Private Entrepreneur

    Vitaliy Levchuk • Chernivtsi, Ukraine

    January 2012 – March 2023
    • • Delivered translation services, IT desktop support, website design, and consulting.
    • • Managed client engagements and operational logistics across service lines.
    • • Since September 2022, added power equipment trading and logistics.
  4. 04

    Lead Clinical Research Associate (LCRA)

    IQVIA • Kyiv Region, Ukraine

    October 2016 – October 2021
    • • Managed clinical trial monitoring, site management, and regulatory compliance.
    • • Oversaw site selection, initiation, and monitoring visits under GCP standards.
    • • Ensured quality documentation and risk-based monitoring practices.
  5. 05

    Associated Director for Science / Project Manager

    Matrixcell s.r.o. • Podebrady, Czechia

    February 2014 – October 2016
    • • Managed pre-clinical and clinical research for a Class III medical device manufacturer.
    • • Led quality management, medical writing, and regulatory affairs.
    • • Coordinated validation of procedures and project documentation.
  6. 06

    Clinical Research Associate Grade II

    TFS Trial Form Support / CTG CRO • Kyiv, Ukraine

    March 2012 – February 2014
    • • Worked as SCRA on a TFS CRO subcontracted project.
    • • Conducted monitoring visits and managed investigative sites.
    • • Ensured protocol compliance and documentation quality.
  7. 07

    Clinical Research Associate (CRA)

    SPRI Clinical Trials

    2011 – 2012
    • • Supported clinical research operations and monitoring activities.
    • • Maintained documentation accuracy and protocol adherence.
  8. 08

    SCRA / Regional Associate Manager (RAM)

    QED Clinical Services Ltd

    June 2010 – June 2011
    • • Delivered site oversight and regional coordination for trials.
    • • Supported monitoring plans and compliance activities.
  9. 09

    Senior Clinical Research Associate (SCRA)

    Worldwide Clinical Trials

    June 2009 – June 2010
    • • Led monitoring visits and ensured protocol compliance.
    • • Maintained site documentation and regulatory readiness.
  10. 10

    Clinical Research Associate (CRA)

    PPD

    October 2008 – February 2009
    • • Transitioned from InnoPharm Ukraine LTD to PPD Global Inc.
    • • Conducted Phase III trials: site selection, initiation, monitoring, and SDV.
    • • Managed regulatory submissions and trial documentation.
  11. 11

    Clinical Research Associate (CRA)

    InnoPharm

    January 2006 – October 2008
    • • Managed Phase III trials across 5 to 14 investigative sites.
    • • Led site selection, initiation visits, SDV, and IP accountability.
    • • Delivered regulatory submissions and maintained trial compliance.
  12. 12

    Quality Control Manager

    PharmPlanNet Clinic / Innovative Pharma Research Eastern Europe GmbH

    August 2004 – December 2005
    • • Oversaw clinical data quality control in a Phase I clinic.
    • • Coordinated on-site activities to ensure protocol compliance.
  13. 13

    Lab Technician (LABMAN)

    Bukovinian State Medical Academy

    March 2004 – June 2004
    • • Supported laboratory operations and technical documentation.
    • • Assisted with routine lab workflows and compliance needs.

Education & Certifications

Academic background and credentials

Structured, recruiter-friendly overview of formal education, certifications, and language proficiency.

Formal Education

Editable

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[Brief note about focus, honors, or thesis topic.]

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Certifications

  • Using Artificial Intelligence at the ICRC

    Credential earned • [Year placeholder]

  • Take an Open Approach to Others' Arguments

    Credential earned • [Year placeholder]

  • Using Artificial Intelligence

    Credential earned • [Year placeholder]

  • IELTS 6.5 (2008)

    English language testing

Languages

English

Full Professional

Verified

Add additional languages as needed for international roles or cross-border collaboration.

Contact

Let’s connect for opportunities and collaboration

If you’re hiring, exploring partnerships, or simply want to connect professionally, I’d be happy to hear from you. Reach out through the channels below and I’ll respond as soon as possible.

Location

Dnipro & Chernivtsi, Ukraine

Availability

Open to roles & advisory projects

Reach me directly

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Email
[email protected]
LinkedIn
linkedin.com/in/vlevchuk/
Phone
+31 6 23147127

Preferred topics

Venture capital, procurement leadership, pharmaceutical research collaboration.