Associate Clinical Data Manager – FSP

Fortrea

. Responsible for the full cycle of Clinical Data Management queries .

Posted 10/2/2026full-timeRemote • Romania, Poland, Estonia, Bulgaria, Greece, HungaryJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Data Management, including project documentation, data validation processes, and adherence to industry standards such as CDASH and SDTM. Capable of leading teams, managing risks, and ensuring timely deliverables in clinical trials.

Highest-signal resume keywords

Clinical Data ManagementProject Documentation DevelopmentCDASH and SDTM KnowledgeTeam Leadership and MentoringClinical Trial Process Expertise

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data Validation ProcessesRisk ManagementClinical OperationsBiometricsQuality Management

Soft Skills

Excellent Communication SkillsPresentation Skills

Certifications & Qualifications

University Degree in Life ScienceNursing CertificationMedical Technology Certification

Industry Keywords

CROPharmaceuticalBiotechnologyEarly Phase TrialsRegulatory Obligations

About the role

Key responsibilities & impact

Responsible for the full cycle of Clinical Data Management queries
Cooperate with Clinical Data Managers, Data Coordinators, Statistical Programmers and others
Assist and lead operations alongside Senior CDM
Develop project documentation, system setup, data validation processes and procedures assigned to junior staff
Work with Senior CDM to build study milestone timelines and follow study timelines for on-time deliverables
Assist or lead internal and external DM meetings
Manage proactively risks and resolve or escalate issues connected to Clinical Data Management improvement or technology
Develop understanding of CDASH and SDTM or other recognized industry standards and their impact on programming teams
Specialize in TA-specific data capture and standards, conduct lessons learned and disseminate them across the organization
May act as a team leader or mentor Clinical Data Management colleagues and stakeholders on operational processes
Lead project-level activities consistent with current or previous experience in support of study delivery

Requirements

What you’ll need

University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
Additional relevant work experience will be considered in lieu of formal qualifications
Experience in clinical data management as a Lead DM or Senior CDA or similar within early phase trials at CRO/pharma level
Excellent oral and written communication and presentation skills
In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations
Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies

Benefits

Comp & perks

Various local benefits such as pension contributions
Complimentary health insurance plans
Remote working allowances
Genuine work life balance
Flexibility in working hours
Thorough onboarding with support from a personal mentor
Permanent employment contract with Fortrea Drug Development
Rewarding career progression
Mentoring, training and personalized development planning