Veristat is a global team with over 30 years of expertise in accelerating life-changing therapies to patients worldwide. The Senior Project Manager will lead complex clinical trial and regulatory projects while collaborating with internal teams and external partners.
Responsibilities:
- Provides 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
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. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis
- Executive level communication, written oral communication, interpersonal skills, as well as strong planning and organizational ability are required
- Good working knowledge of drug development process and regulatory requirements, including familiarity with International Conference on Harmonisation (ICH) guidelines and other applicable regulatory rules and guidelines
- Proficiency in English (written and verbal)
- Action-oriented and resilient in a fast-paced environment and will have the ability to lead high performing cross functional project teams, motivate others, delegate, including advanced stakeholder communication/ escalation problem solving and decision-making skills
- Ability to build, manage relationships with internal and external team members (vendors, clients etc.) and drive activities to conclusion with minimal support
- Ability to mentor and delegate