Clinical Trial Assistant – Supply

Fortrea

. Manage clinical and non-clinical supply in collaboration with other country roles .

Posted 10/19/2026full-timeIstanbul • TurkeyJuniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical supply management and documentation processes, with a strong understanding of ICH-GCP guidelines and the clinical trial process. Proficient in managing clinical trial databases and ensuring compliance with quality control standards.

Highest-signal resume keywords

Clinical Supply ManagementICH-GCP GuidelinesClinical Trial ProcessETMF Quality ControlClinical Research Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Document ManagementDatabase UpdatingLabeling Requirements ManagementTranslation Change CoordinationETMF Reconciliation

Soft Skills

PlanningOrganizationTime ManagementProblem-SolvingCommunication

Tools & Technologies

CTMSETMF

Certifications & Qualifications

Nursing LicensureMedical Technology CertificationLaboratory Technology Certification

Industry Keywords

Clinical ResearchSupply Chain ManagementIHCRACTASupply CTA

About the role

Key responsibilities & impact

Manage clinical and non-clinical supply in collaboration with other country roles
Collate, distribute/ship, and archive clinical documents
Manage labeling requirements and coordinate/sign translation change requests
Prepare documents and correspondence
Ensure collection and distribution of study tools and documents
Update clinical trial databases (CTMS) and trackers
Assist with eTMF reconciliation
Document proper destruction of clinical supplies
Execute the eTMF Quality Control Plan

Requirements

What you’ll need

University or college degree (biological or life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology)
Understanding of ICH-GCP guidelines
Understanding of the clinical trial process
Minimum of 1.5 years of industry experience in a related role (e.g., IHCRA, CTA, Supply CTA)
Experience in clinical research supply management processes preferred
Good planning, organization, time management and problem-solving skills
Good communication skills, oral and written
Ability to work efficiently and effectively in a matrix environment

Benefits

Comp & perks

Permanent, full-time contract
Excellent exposure to a range of disease areas
Opportunity for career progression and promotion