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Syneos Health

Clinical Data Reviewer - Oncology Required (US, CAN, UK Only)

London
$80.6k – $145k/yr
Posted 6 days ago
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Clinical Data Reviewer - Oncology Required (US, CAN, UK Only)

Clinical Data Reviewer - Oncology

Location: US, CAN, UK (In-Situ Only)

About the Role

At Syneos Health®, a leading life sciences services organization, we empower our partners across the drug development continuum with integrated expertise to navigate complexity, anticipate change, and accelerate progress. Our Clinical Solutions team combines deep therapeutic area knowledge with a mindset focused on driving customer success—whether through targeted partnerships or full-service solutions.

This agile and results-driven role involves collaborative problem-solving to support pivotal milestones in oncology drug development. A Clinical Data Reviewer provides critical scientific and clinical validation of study data, ensuring integrity ahead of submissions, analyses, and real-world evidence applications.


Key Accountabilities

The Clinical Data Reviewer performs specialized clinical assessments and interpretable queries on large-scale oncology trials, acting as an extension of clinical scientists. Responsibilities include:

  • Data Quality & Review:

    • Ensure data readiness for critical milestones (e.g., interim/final analyses, submission snapshots, Data Monitoring Committees).
    • Validate patient-level data against CRF Completion Guidelines (CCGs) and Data Review Plans (DRPs).
    • Conduct point-to-point data checks (e.g., verifying patient eligibility criteria via lab results) and interpretive checks (e.g., signal detection for inconsistencies).
  • Query Management:

    • Generate high-quality queries on discrepant or invalid data, document resolutions, and escalate unresolved issues.
    • Follow-up on queries to close loops and ensure accuracy.
  • Trend & Signal Identification:

    • Apply data review best practices & tools to detect potential safety trends/signals from large multi-site datasets.

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£35,000/yr

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  • Protocol Deviation & Compliance:

    • Identify protocol deviations during routine review; escalate as needed.
    • Strict adherence to SOP policies, regulations, and training requirements, with a commitment to quality improvements.
  • Collaboration & Communication:

    • Liaise with data management, clinical teams, site management, and study leadership as required.
    • Attend clinical meetings and study migration checks virtually/in-person.

Requirements

Education & Credentials:

  • Bachelor’s degree or equivalent in Medical/Science, Clinical Research, or Nursing (mandatory).

Experience & Skills:

  • 7+ years in pharmaceutical clinical research, with strong monitoring/clinical review experience sought.
  • Hands-on clinical review experience: Direct query writing, validation methodologies, and interpretation of data trends, safety signals.
  • Oncology exposure is required.
  • Prescriber’s knowledge of investigational products, concomitant medications, and clinical accuracy essential.
  • EDC (Electronic Data Capture) familiarity – preferred but not mandatory.
  • Excel proficiency for reviewing large datasets (filters, sorting, date formatting).
  • Basic understanding of CRF design, data editing checks, and data-handle conventions.

Operational & Soft Skills:

  • Ability to work independently in a virtual setting or in a hybrid team.
  • Agile prioritization: Balancing multiple projects/queries under tight deadlines with flexibility.
  • Strong communication (written/oral) with meticulous attention to detail.
  • Compliance adherent; seeks opportunities to improve efficiency and quality.

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Location & Visa: US, UK, or Canada citizens/residents only; no sponsorship available.


About Syneos Health

Support & Development:

  • Supportive career growth through leadership, training (technical + peer recognition).
  • Inclusive culture fully embracing diversity – individuality is not just allowed, but valued.
  • Resilience & determination: Our employees embody "Driven to Deliver" – every effort shapes solutions that directly impact healthcare delivery at scale.

Supporting Assets at Syneos:

Our robust World-Class partners portfolio covers 94% of new FDA-approved drugs and 95% of EMA-authorized products across 70,000+ sites globally >675K patients. Our work is nothing short of ground-breaking – and we do it together, with a relentless push toward innovation.

Why Join Us?

  • Relevant oncology experience + clear career advancement.
  • Flexible teams, global diversity (yet “чувствие семьи” – “family feel).
  • Transparency: "No Unsatisfied Clients" guarantee – our impact equals our success.

Benefits Highlights:

  • Competitive total compensation with base ranging $80.6K–$145K, plus:
    • Corporate car allowance/#attrition# /company car poèmes
    • Comprehensive health & well-being benefits (Health, Dental, Vision)
    • A 401(k) plan matched by the company
    • Stock purchase plan and opfitable commissions/bonuses (Tier 1/colleagues).
    • Flexible PTO policy (~variant jurisdiction-based paid sick-leave).

Next Steps

Informal inquiries:

  • Learn more.

(Optional disclaimers inline – separate section omitted for brevity.)


Apply here: Syneos Health website


Federal/local jurisdiction employment laws apply. No contract employment implied.

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Skills

Clinical Review
Data Analysis
Oncology
Query Writing
Data Management
Microsoft Excel
Clinical Research
Protocol Deviations
SOP Compliance
Communication Skills
Attention to Detail
Problem Solving
Team Collaboration
Therapeutic Area Knowledge
Data Review Tools

Location

London, England, United Kingdom

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