Remote Medical/Clinical Scientist: Bladder Late Phase

Syneos Health/ inVentiv Health Commercial LLC; Georgia; Remote; USD 68,000 - 140,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits

401k

Stock Purchase Plan

Bonuses

Paid time off

Job summary

Syneos Health is seeking a Medical/Clinical Scientist - ONC - Bladder Late Phase for sponsor-dedicated remote work in the United States. You will partner with Medical Directors to design medical plans, review data, and ensure safety and data integrity across studies.

The role involves cross-functional collaboration with Clinical Operations, Data Management, Drug Safety, and Project Management to meet milestones. Strong knowledge of ICH/GCP required.

Responsibilities

• Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan).
• Performs regular and ad-hoc medical review of data listings and data visualization; analyzes the data to identify risks and trends and supports documentation of reviews.
• Authors medical data queries and reviews query responses, approves query closure with Medical Director.
• Assists Medical Director in patient profiles review and protocol-related data reviews as needed.
• Partners with Medical Directors for data review meetings and safety review meetings, including slide preparation.
• Manages project scope, objectives, and deliverables to meet milestones; interfaces with internal teams, customers, and vendors.
• Collaborates with Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, and Project Management to identify data risks; escalates concerns promptly.
• May participate in internal and external audits.
• Gains understanding of protocol designs and disease terminology; adheres to data privacy, ICH, and GCP guidelines.
• May participate in interviews.

Job description

Syneos Health is seeking a Medical/Clinical Scientist - ONC - Bladder Late Phase for sponsor-dedicated remote work in the United States. You will partner with Medical Directors to design medical plans, review data, and ensure safety and data integrity across studies.

The role involves cross-functional collaboration with Clinical Operations, Data Management, Drug Safety, and Project Management to meet milestones. Strong knowledge of ICH/GCP required.