Respiratory Clinical Scientist: Data-Driven Medical Expert

Syneos Health/ inVentiv Health Commercial LLC; Jackson (MS); Vor Ort; USD 90.000 - 130.000; Vollzeit

Benefits dieser Stelle

Company car

Health benefits

401k match

Stock purchase plan

Bonus potential

Paid time off

Zusammenfassung

Syneos Health is seeking a Clinical Scientist - Respiratory to lead medical data review, develop medical management plans with the Medical Director, and coordinate external input for study design. You will perform regular and ad-hoc medical data reviews, author data queries, and support safety review meetings, while ensuring compliance with ICH, GCP, and project plans across global teams.

Join a collaborative environment where patient outcomes and scientific rigor guide our work and where

Aufgaben

• Works with Medical Director to develop medical plans and coordinate input from outside experts to prepare medical plans.
• Performs regular and ad-hoc medical data reviews and analyzes data for risks and trends; supports documentation of reviews.
• Authors medical data queries and reviews responses; closes queries with Medical Director.
• Assists in patient profiles review, protocol deviation reviews, and Medical Review Summary reports as needed.
• Partners with Medical Directors for data review and safety review meetings, including slide preparation.
• Manages project scope, milestones and timelines; acts as primary interface between internal team, customers and vendors.
• Collaborates with Clinical Operations, Data Management, Drug Safety, and Project Management to identify risks related to data integrity and subject safety.
• Attends Trusted Process meetings and may participate in audits.
• Gains understanding of ongoing protocol designs and disease terminology.
• Adheres to data privacy, ICH, GCPs and enterprise policies.

Jobbeschreibung

Syneos Health is seeking a Clinical Scientist - Respiratory to lead medical data review, develop medical management plans with the Medical Director, and coordinate external input for study design. You will perform regular and ad-hoc medical data reviews, author data queries, and support safety review meetings, while ensuring compliance with ICH, GCP, and project plans across global teams.

Join a collaborative environment where patient outcomes and scientific rigor guide our work and where