Senior Clinical Development & Medical Affairs Strategist

Alcon; Johns Creek (GA); Presencial; USD 140.000 - 180.000; Jornada completa

Descripción de la vacante

Alcon is seeking a Sr. Clinical Development and Medical Affairs Project Lead to direct planning, timelines, and execution of clinical studies from Johns Creek, GA, in the United States.

You will gather input from cross-functional teams to ensure on-schedule deliverables and oversee study operations in line with SOPs, GCP, and regulatory requirements. The role emphasizes collaboration across teams, development of study budgets, and maintaining protocol compliance, with relocation available and

Formación

• Bachelor's Degree or Equivalent years of directly related experience (or high school+15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs)
• The ability to fluently read, write, understand, and communicate in English
• 7 Years of Relevant Experience
• Travel Requirements: Up to 15%

Responsabilidades

• Gather input from cross-functional teams and create plans that help the team produce deliverables on schedule
• Ensuring consistency of clinical study and processes across clinical trials
• Overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with SOP, GCP and country regulations such as site and vendor selection, preparing clinical trial budgets
• Ensuring study is conducted within clinical trial protocols
• Monitoring progress and following up with team members and line managers when issues develop
• Implementing and preparing the clinical development strategy as outlined by the clinical teams
• May develop recruitment strategy for the trial in program

Conocimientos

Cross-functional collaboration

Clinical study timelines

Budget planning

Educación

Bachelor's degree or equivalent

Descripción del empleo

Alcon is seeking a Sr. Clinical Development and Medical Affairs Project Lead to direct planning, timelines, and execution of clinical studies from Johns Creek, GA, in the United States.

You will gather input from cross-functional teams to ensure on-schedule deliverables and oversee study operations in line with SOPs, GCP, and regulatory requirements. The role emphasizes collaboration across teams, development of study budgets, and maintaining protocol compliance, with relocation available and