Remote Medical/Clinical Scientist, Bladder Late Phase

Syneos Health/ inVentiv Health Commercial LLC; Delaware; À distance; USD 68 000 - 140 000; Plein temps

Avantages offerts par ce poste

Company car or car allowance

Health benefits (Medical, Dental and V

Vision

Company match 401k

Employee Stock Purchase Plan

Commissions/bonus based on company and

flexible paid time off (PTO) and sick

Résumé du poste

Syneos Health is seeking a Medical/Clinical Scientist to support ONC in bladder late‑phase trials from a sponsor‑dedicated remote role. You will work with Medical Directors to develop medical plans and coordinate input from external experts.

Responsibilities include regular and ad‑hoc medical data reviews, issuing data queries, and preparing Medical Review summaries. You will partner with study teams to manage scope, timelines, and deliverables, and participate in audits while upholding ICH/GCP

Responsabilités

• Works with Medical Director to develop medical plans and coordinate input from external experts/consultants/advisors.
• Performs regular and ad-hoc medical data reviews; analyzes data to identify risks and patterns; supports documentation.
• Authors medical data queries and reviews query responses; approves query closure with Medical Director.
• May assist Medical Director in patient profiles review and study‑level data review.
• Partners with Medical Directors for medical data review meetings and safety review meetings.
• Manages project scope, objectives, and deliverables; serves as primary interface between internal team, customers, and vendors.
• Collaborates with study team members across Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management.
• Participates in internal and external audits.
• Adheres to data privacy, ICH and GCPs, enterprise policies and project plans.
• May participate or conduct interviews.

Description du poste

Syneos Health is seeking a Medical/Clinical Scientist to support ONC in bladder late‑phase trials from a sponsor‑dedicated remote role. You will work with Medical Directors to develop medical plans and coordinate input from external experts.

Responsibilities include regular and ad‑hoc medical data reviews, issuing data queries, and preparing Medical Review summaries. You will partner with study teams to manage scope, timelines, and deliverables, and participate in audits while upholding ICH/GCP