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Clinical Data Reviewer - Oncology

Job in Philadelphia, Philadelphia County, Pennsylvania, 19117, USA
Listing for: Syneos Health
Full Time position
Listed on 2026-07-14
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 80600 USD Yearly USD 80600.00 YEAR
Job Description & How to Apply Below
Position: Clinical Data Reviewer - Oncology Required (US, CAN Only)

Clinical Data Reviewer – Oncology (US, CAN Only)

We are looking for an experienced Clinical Data Reviewer with oncology expertise to play a key role in ensuring data integrity and quality for clinical trials.

Role Responsibilities
  • Ensure data readiness for important milestones including interim analysis, final analysis, snapshots to support submissions, Data Monitoring Committee reviews, and publications.
  • Review participant‑level data across a study in adherence to CRF Completion guidelines (CCGs) and the Data Review Plan (DRP).
  • Conduct point‑to‑point data checks and interpretive analysis to identify inconsistencies or errors.
  • Generate queries on discrepant data and follow to resolution, escalating issues that cannot be resolved through the query process.
  • Create and use data review best practices and tools to identify trends and safety signals.
  • Identify protocol deviations during routine clinical review and escalates as appropriate.
  • Follow relevant SOPs and regulations, maintain excellent training compliance, and continually seek improvements in quality and efficiency.
  • Liaise with data management, clinical, and site management teams as required.
  • Attend clinical meetings and study milestones.
Qualifications
  • Industry experience in oncology is required.
  • Must reside in the US or Canada with no sponsorship needed.
  • Bachelor’s degree, nursing degree, or equivalent is preferred.
  • At least 7 years of clinical research experience in the pharmaceutical industry (strong monitoring experience a plus).
  • Minimum 3 years of oncology experience.
  • Direct clinical review and query writing/resolution experience required.
  • Ability to assess whether participant data is scientifically and clinically valid.
  • Prior EDC experience preferred.
  • Proficient in reviewing large-scale listings in Microsoft Excel (filter, sort, date formatting).
  • Basic understanding of how data points from different fields/CRFs interact and how data collection impacts analysis.
  • Ability to work independently in a virtual setting and as part of a remote team.
  • Strong ability to prioritize and adjust work priorities quickly to meet deadlines.
  • Basic knowledge of data management including case report form design, electronic edit checks, data handling conventions, and interpretation of data status reports.
  • Strong written and oral communication skills with strong attention to detail.
Benefits and Compensation

Salary range: $80,600.00 – $. Benefits may include a company car or allowance, health benefits (medical, dental, vision), company match 401(k), employee stock purchase plan eligibility, commission/bonus opportunities, flexible paid time off and sick leave. Paid sick time eligibility varies by state or municipality.

EEO Statement

We are committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. The Company is committed to compliance with the EU Equality Directive and all applicable federal, state, and municipal paid sick time requirements. The Company is the sole discretion to determine what constitutes as equivalent to the qualifications described above.

No employment contract is created by this statement.

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