Syneos Health Careers 2026 | Clinical Data Reviewer Jobs (Oncology Remote US UK Canada)

Syneos Health Careers 2026 | Clinical Data Reviewer Jobs (Oncology Remote US UK Canada) Syneos Health Hiring | Clinical Data Reviewer (Oncology Specialist) – Remote US, UK & Canada

Bachelor's Degree /

B.Sc Nursing

7+ Years Clinical Research & Mandatory Oncology Exp

Are you searching for remote clinical data reviewer jobs in oncology
, senior clinical reviewer careers at Syneos Health
, or EDC query management and data review specialist vacancies in CROs
? Global biopharmaceutical solutions leader Syneos Health® is actively hiring for the position of Clinical Data Reviewer
- Oncology (Job : ).

In this full-time remote role, you will act as a key clinical expert working alongside medical monitors and clinical scientists to perform participant-level clinical data reviews, trend analyses, and EDC query management across complex Phase III oncology trials. Candidates holding a Bachelor's degree or Nursing degree with at least 7 years of clinical research experience in pharma/CROs and direct hands-on oncology clinical review experience are eligible to apply.

The base salary range for this role is $80,600 – $145,000 USD per annum plus comprehensive benefits.

• Job Title: Clinical Data Reviewer
  - Oncology
• Job :
• Work Location: Remote / Home-Based (Candidates must reside in US, UK, or Canada without sponsorship)
• Employment Type: Full-Time, Permanent
• Salary Range: $80,600.00 – $ USD per annum
• Educational Background: Bachelor's Degree in Life Sciences or Nursing degree preferred
• Experience
  
  Required:
  
  Minimum 7+ years of clinical research experience in pharma/CRO; mandatory direct Oncology domain experience
• Core Technical Systems: Electronic Data Capture (EDC) systems, Data Review Plan (DRP), CRF Completion Guidelines (CCGs), Large-scale Excel data listings
• Date Posted: 03 August 2026

As a Clinical Data Reviewer (Oncology) at Syneos Health, your core duties will include:

• Milestone Data Readiness: Ensure clinical data cleanliness and readiness ahead of key trial milestones, including interim analyses, study closeouts, regulatory submission snapshots, Data Monitoring Committee (DMC) reviews, and scientific publications.
• Participant-Level Clinical Review: Perform rigorous point-to-point and interpretive clinical data reviews across participant records in adherence with Case Report Form (CRF) Completion Guidelines (CCGs) and the study Data Review Plan (DRP).
• Query Generation & Escalation: Draft, issue, and resolve clinical queries on discrepant or inconsistent participant data (e.g., verifying lab values against inclusion criteria, drug-concomitant medication interactions), escalating unresolved issues to medical leads.
• Trend Analysis & Safety Signal Identification: Utilize data review tools and large-scale Excel data listings to identify data trends, protocol deviations, and potential safety signals.
• Cross-Functional Collaboration: Work closely as an extension of the clinician/clinical scientist team, collaborating with Data Management (DM), Clinical Research Associates (CRAs), and site personnel.
• Bachelor's degree in Life Sciences, Allied Health, or
  
  B.Sc Nursing degree (Preferred).

Required Experience &

Competencies:

• At least 7 years of clinical research experience in the pharmaceutical or CRO industry (Strong CRA / Clinical Research Associate monitoring experience is a major plus).
• Mandatory: Direct hands-on clinical research and data review experience in Oncology trials.
• Proven experience conducting clinical data reviews, writing clinical queries, and resolving data discrepancies.
• Deep therapeutic knowledge of oncology disease processes, expected investigational drug effects, adverse event profiles, and concomitant medications.
• Hands-on proficiency with Electronic Data Capture (EDC) systems and advanced Excel data listing analysis (filtering, sorting, date-formatting).
• Understanding of basic data management workflows, edit checks, CRF design, and data status reports.
• Must reside in the US, UK, or Canada with full authorization to work (no visa sponsorship provided).
• Partner with a premier global CRO that has worked with 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products over the past 5 years.
• Collaborate…