Remote Oncology Clinical Scientist - Data & Medical Review

Syneos Health, Inc.; Utah; Hybrid; USD 120,000 - 170,000; Full time

Benefits offered by this job

Company car/Car allowance

Medical, Dental, Vision benefits

Company match 401k

Employee Stock Purchase Plan

Job summary

Syneos Health in the United States seeks a Clinical Scientist - Oncology to join its Clinical Development team. The role emphasizes protocol-specific requirements, scientific integrity, and cross-functional collaboration to advance clinical trials.

The successful candidate will work with Medical Directors and other teams to review data, interpret findings, and ensure adherence to ICH/GCP guidelines while contributing to the scientific execution of early- and late-stage studies.

Responsibilities

• Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans.
• Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews.
• Authors medical data queries and reviews query responses, approves query closure in association with Medical Director.
• May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed.
• Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed.
• Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review.
• Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management to identify risks related to data integrity and subject safety, escalating concerns as needed.
• Attends Trusted Process meetings and may participate in internal and external audits.
• Acquires basic understanding of ongoing protocol designs and disease-related terminology and pathology.
• Adheres to data privacy guidelines, ICH, GCPs, and all enterprise policies and project plans.
• Adheres to customer policies and standard operating procedures, as required in project plans.

Job description

Syneos Health in the United States seeks a Clinical Scientist - Oncology to join its Clinical Development team. The role emphasizes protocol-specific requirements, scientific integrity, and cross-functional collaboration to advance clinical trials.

The successful candidate will work with Medical Directors and other teams to review data, interpret findings, and ensure adherence to ICH/GCP guidelines while contributing to the scientific execution of early- and late-stage studies.