Project Leadership - Biotech (clinical trials) -Neurology/Psych/Rare Disease

Role Description

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, your work has a direct impact on the projects, teams, and clients you work with, while helping deliver projects to the benefit of the patients we serve.

Parexel’s defined Biotech Division offers opportunities for seasoned Project Management professionals with a strong background running global clinical trials in a variety of therapeutics. This group focuses specifically on Biotech clients and providing all areas of support to accommodate their unique needs. This is a great opportunity for those in the industry who prefer the flexibility, creativity, and problem-solving mindset to successfully support this type of clients.

Parexel has upcoming opportunities at the Project Leader (PM) and Senior Project Leader (SPM) level for candidates with experience leading global studies in Neurology/Psych/Rare Disease.

• Provide leadership to project teams
• Manage day-to-day operations
• Aim for operational excellence through on-time delivery within budget and to the highest quality
• Strive to exceed client expectations

Qualifications

• Undergraduate degree in a clinical or health-related field; advanced degree preferred
• Minimum of 2+ years' experience leading Global Clinical Trials in Project Management within a CRO (preferred), Biotech, or Pharma company
• Experience in project scheduling, managing resources and budgets, and coordinating team activities
• Experience with the full clinical development process through regulatory submissions
• Additional years of experience required for more senior roles (Senior Project Leader, Associate Project Director, Project Director)

Requirements

• Flexibility and problem-solving capabilities
• Strategic vision
• Detail-oriented
• Computer proficient
• Superior interpersonal and organizational skills

Benefits

• Equal opportunity employer
• Consideration for employment without regard to legally protected status