Sr. Principal I, Clinical Project Management

The Sr. Principal II, Clinical Project Management, is primarily responsible for serving as a global/regional clinical expert throughout the product lifecycle, from development to post-market monitoring. You will build effective relationships across teams, implement clinical strategies, and ensure compliance with protocols.

In this role, a typical day will include:

• Leading projects leveraging clinical data and developing clinical content
• Implementing and preparing the clinical development strategy as outlined by the clinical sub-teams or workstreams
• Gathering input from cross-functional teams and creating plans that help the team produce deliverables on schedule
• Planning, directing, creating, and communicating clinical study timelines
• Ensuring consistency of clinical study and processes across clinical trials
• Ensuring study is conducted within clinical trial protocols
• Monitoring progress and following up with team members and line managers when issues develop
• Overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations
• Participating in data analysis, interpretation and synthesis, instruction in order to develop Clinical study report and/or support development of scientific publications including peer reviewed manuscripts in partnership with external key opinion leaders (KOLs)

WHAT YOU’LL BRING TO ALCON:

• 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

Preferred:

• Ophthalmology experience (Glaucoma Preferred)

Other:

• Travel Requirements: up to 20% International and/or Domestic