[Hiring] Project Leadership - Real-World Evidence - (RWE clinical trials) @Parexel

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, helping to deliver projects to the benefit of the patients we serve.

The Global Project Leadership department has dedicated members at all levels who are aligned to work with specific types of clients and deliver solutions customized to fit those client’s needs, working on projects spanning across all phases of global clinical trials, in a wide array of therapeutic areas.

Parexel has an opportunity at the Senior Project Leader (SPM) level for a candidate with experience leading global studies in a variety of therapeutics with a strong background in Real-World Evidence (RWE) programs.

• Provide leadership to project teams and manage day-to-day operations.
• Strive to achieve operational excellence through on-time delivery within budget and to the highest quality.
• Exceed client expectations.

Qualifications

• Undergraduate degree in a clinical or health-related field; advanced degree preferred.
• Minimum 3+ 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.

Requirements

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

Company Description

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.