Provide management and leadership to plan, prepare, and execute complex and high-profile clinical trial or Regulatory projects and/or programs.
Interface with internal departments and company leadership, and externally with sponsors and vendors.
Drive activities to conclusion with minimal support and mentor team members.
Requirements
Bachelor’s degree in life/health sciences or related discipline, or equivalent required.
5 to 8 years of Project Management experience leading global/complex clinical trials in a Clinical Research Organization/Pharmaceutical Company
Executive level communication, written oral communication, interpersonal skills, strong planning and organizational ability required.
Good working knowledge of drug development process and regulatory requirements, including familiarity with International Conference on Harmonisation (ICH).
Proficiency in English (written and verbal).
Action-oriented and resilient in a fast-paced environment.
Ability to lead high performing cross functional project teams, motivate others, and manage relationships with internal and external team members, including vendors, clients, etc.
Advanced stakeholder communication, escalation problem solving, and decision-making skills.