Remote Cardiovascular Clinical Scientist

Syneos Health, Inc.; North Dakota; Hybrid; USD 120,000 - 150,000; Full time

Benefits offered by this job

Health benefits

401k match

Stock Purchase Plan

Commissions/bonus

Flexible PTO

Job summary

Syneos Health is seeking a remote US-based professional to support clinical development through medical plan development, data reviews, and cross-functional collaboration. You will work with Medical Directors to ensure data integrity, safety, and regulatory compliance across study timelines.

The role involves coordinating with external experts, preparing data reviews, and participating in audit and process improvement activities within a dynamic, global organization.

Responsibilities

• Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan).
• Engages with outside experts to coordinate medical inputs for plans.
• Performs regular and ad-hoc medical review of data listings and data visualization; analyzes data to identify risks and trends.
• Authors medical data queries and reviews query responses; approves query closure with Medical Director.
• May assist Medical Director in patient profiles review, scientific review of other study data, protocol deviation review.
• Partners with Medical Directors for data review meetings and safety review meetings including slide prep.
• Manages project scope, objectives, and deliverables; interfaces with internal team, customers, and vendors.
• Collaborates with study team members to identify risks related to data integrity and subject safety; escalates concerns.
• Attends Trusted Process meetings; may participate in audits.
• Acquires knowledge of ongoing protocol designs and disease terminology.
• Adheres to data privacy guidelines, ICH, GCPs, and enterprise policies.

Job description

Syneos Health is seeking a remote US-based professional to support clinical development through medical plan development, data reviews, and cross-functional collaboration. You will work with Medical Directors to ensure data integrity, safety, and regulatory compliance across study timelines.

The role involves coordinating with external experts, preparing data reviews, and participating in audit and process improvement activities within a dynamic, global organization.