About The Position

Parexel’s Global Project Leadership organization drives success for clients and advances clinical research projects across global trials, therapeutic areas, and phases of development. The Partnership Division works with large dedicated clients and established partnerships, providing tailored support in a fast-paced, high-profile client environment. Parexel is hiring at the Project Leader and Senior Project Leader levels for professionals with experience leading global studies in areas including Oncology, Cell and Gene Therapy, Rare Disease, and Cardiology. In these roles, you will lead project teams and manage day-to-day operations, pursuing on-time delivery within budget and to high quality standards while aiming to exceed client expectations. The role calls for project management experience across the full clinical development process, including regulatory submissions, as well as flexibility, problem-solving ability, and strategic vision. The posting describes the opportunity as home-based.

Requirements

  • Undergraduate degree in a clinical or health-related field.
  • At least 2 years of experience leading global clinical trials in project management.
  • Experience in project scheduling, resource and budget management, and coordinating team activities.
  • Experience with the full clinical development process through regulatory submissions.
  • Flexibility, problem-solving capabilities, and strategic vision.
  • Attention to detail, computer proficiency, and superior interpersonal and organizational skills.

Nice To Haves

  • Advanced degree preferred.
  • CRO experience preferred; experience in a biotech or pharmaceutical company is also accepted.
  • Experience in Oncology, Cell and Gene Therapy, Rare Disease, or Cardiology.
  • Additional years of experience for Senior Project Leader, Associate Project Director, and Project Director roles.

Responsibilities

  • Provide leadership to project teams.
  • Manage day-to-day project operations.
  • Drive operational excellence and deliver projects on time, within budget, and to high quality standards.
  • Coordinate team activities and manage project schedules, resources, and budgets.
  • Support global clinical trials through the full clinical development process, including regulatory submissions.
  • Work with large dedicated clients and established partnerships to provide support suited to their needs.
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