Global Clinical Project Lead - Senior Principal

Regulatory Toolkit; Fort Worth (TX); Vor Ort; USD 140.000 - 200.000; Vollzeit

Zusammenfassung

Alcon is seeking a Sr. Principal II, Clinical Project Management for an onsite role based at Fort Worth, TX or Lake Forest, CA.

You will serve as a global/regional clinical expert across the product lifecycle, partnering with cross-functional teams to implement clinical strategies and ensure compliance with protocols. Daily tasks include leading projects with clinical data, developing study timelines, coordinating cross-functional input, and ensuring trials align with SOPs and GCP.

Qualifikationen

• Bachelor's Degree or Equivalent years of directly related experience; fluency in English; 7 Years of Relevant Experience

Aufgaben

• 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 SOPs, GCP and 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 with KOLs

Ausbildung

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.)

Jobbeschreibung

Alcon is seeking a Sr. Principal II, Clinical Project Management for an onsite role based at Fort Worth, TX or Lake Forest, CA.

You will serve as a global/regional clinical expert across the product lifecycle, partnering with cross-functional teams to implement clinical strategies and ensure compliance with protocols. Daily tasks include leading projects with clinical data, developing study timelines, coordinating cross-functional input, and ensuring trials align with SOPs and GCP.