Remote Clinical Scientist: Medical Data & Trial Insights

Syneos Health, Inc.

Illinois

Hybrid

USD 90,000 - 140,000

Full time

14 days+
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Benefits offered by this job

Company car or car allowance
Health benefits
401k
Stock Purchase Plan
Bonus eligibility
PTO & sick time

Job summary

Syneos Health, Inc. is seeking a clinical data professional to support medical data review and plan development for late‑ and early‑stage trials. You will work closely with Medical Directors, cross‑functional teams, and external experts to ensure scientific integrity and data quality.

The role emphasizes data reviews, query responses, and collaboration across Clinical Operations, Data Management, and Pharmacovigilance to address data integrity and subject safety in a fast‑paced environment.

Qualifications

  • Strong understanding of medical data review processes.
  • Experience communicating with medical directors and cross-functional teams.
  • Knowledge of ICH/GCP guidelines and compliance requirements.

Responsibilities

  • Develop medical plans with Medical Director and coordinate inputs.
  • Regularly review data listings and visualization; identify risks and trends.
  • Prepare medical data queries and close queries with Medical Director.
  • Support protocol development, safety review meetings, and slide preparation.
  • Manage project scope, milestones, and stakeholder communication.
  • Collaborate with Clinical Operations, Data Management and Pharmacovigilance.
  • Participate in audits and ensure data privacy and GCP compliance.

Skills

Medical data review
Data visualization
Regulatory compliance
Clinical collaboration

Job description

Syneos Health, Inc. is seeking a clinical data professional to support medical data review and plan development for late‑ and early‑stage trials. You will work closely with Medical Directors, cross‑functional teams, and external experts to ensure scientific integrity and data quality.

The role emphasizes data reviews, query responses, and collaboration across Clinical Operations, Data Management, and Pharmacovigilance to address data integrity and subject safety in a fast‑paced environment.

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