Remote Ophthalmology Clinical Scientist – Data Review

Syneos Health, Inc.; Wyoming (OH); Hybrid; USD 100,000 - 180,000; Full time

Benefits offered by this job

Company car

Health benefits (Medical, Dental, Vis­

401k matching

Employee Stock Purchase Plan

Bonus eligibility

Flexible PTO and sick time

Job summary

Syneos Health in Remote, WY seeks a Clinical Scientist - Ophthalmology to support clinical development programs with a focus on medical data review and protocol-specific requirements. You will collaborate with Medical Directors and external experts to ensure scientific integrity and data quality in trials.

The role emphasizes coordination of medical plans, data reviews, and safety assessments across study teams, with opportunities to contribute to early and late-stage programs in ophthalmology.

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.

Job description

Syneos Health in Remote, WY seeks a Clinical Scientist - Ophthalmology to support clinical development programs with a focus on medical data review and protocol-specific requirements. You will collaborate with Medical Directors and external experts to ensure scientific integrity and data quality in trials.

The role emphasizes coordination of medical plans, data reviews, and safety assessments across study teams, with opportunities to contribute to early and late-stage programs in ophthalmology.