Oncology Prostate Medical Scientist - Clinical Data

Syneos Health; New York (NY); On-site; USD 68,000 - 115,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, Vizn

401k match

Employee Stock Purchase Plan

Bonus eligibility

Flexible PTO & sick time

Job summary

Syneos Health is seeking a Clinical/Medical Scientist - Oncology (Prostate) in the United States. The role focuses on developing medical plans with the Medical Director, reviewing data listings, and coordinating input from external experts to ensure rigorous scientific integrity in trial data.

The position involves cross-functional collaboration with Clinical Operations, Data Management, Drug Safety, and PV, plus engagement in safety reviews, data quality assurance, and adherence to ICH/GCP

Responsibilities

• Works with Medical Director to develop medical plans and coordinates input from external experts to prepare medical plans.
• Performs regular and ad-hoc medical review of data listings and visualizations; analyzes data to identify risks and trends.
• Authors medical data queries and reviews responses; approves query closure with Medical Director.
• May assist in patient profile reviews and scientific review of study data as needed.
• Partners with Medical Directors for data review meetings and safety review meetings, including slide prep.
• Manages project scope, milestones, and deliverables; serves as primary interface between internal team, customers, and vendors.
• Collaborates with Clinical Operations, Data Management, Drug Safety, and PV; escalates risks to project leads.
• Attends Trusted Process meetings; may participate in audits.
• Gains understanding of protocol designs and disease terminology; adheres to ICH, GCPs, and enterprise policies.

Job description

Syneos Health is seeking a Clinical/Medical Scientist - Oncology (Prostate) in the United States. The role focuses on developing medical plans with the Medical Director, reviewing data listings, and coordinating input from external experts to ensure rigorous scientific integrity in trial data.

The position involves cross-functional collaboration with Clinical Operations, Data Management, Drug Safety, and PV, plus engagement in safety reviews, data quality assurance, and adherence to ICH/GCP