Project Leadership - Mid/Large- (clinical trials) - Homebased

Parexel

$110K — $130K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Undergraduate degree in a clinical or health-related field; advanced degree preferred.
  • Minimum 2+ years leading Global Clinical Trials in Project Management within CRO, Biotech, or Pharma.
  • Experience in project scheduling, managing resources and budgets.
  • Knowledge of the full clinical development process, including regulatory submissions.
  • Superior interpersonal and organizational skills.

Responsibilities

  • Provide leadership to project teams and manage daily operations.
  • Strive for operational excellence through timely and budget-conscious project delivery.
  • Exceed client expectations in project outcomes and quality.
  • Coordinate team activities and ensure effective resource management.
  • Customize solutions for mid to large size biotech/pharma clients across various therapeutic areas.

Benefits

  • Opportunity to work with a diverse range of therapeutic projects.
  • Impactful work that directly benefits patient outcomes.
  • Dynamic team environment with dedicated members at all levels.
  • Flexible role that encourages problem-solving and strategic thinking.
Full Job Description

Parexel has opportunitiesin a variety of therapeutics at the Project Leader (PM), Senior Project Leader (SPM) and Project Director level for candidates with experience leading global studies in a variety of therapeutics supporting mid to large-size biotech/ pharma clients.

Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations

Successful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with a minimum, 2+ years' experience leading Global Clinical Trials in Project Management within a CRO (preferred), Biotech or Pharma company. These positions also require experience in project scheduling, managing resources and budgets and coordinating team activities, as well as experience with the full clinical development process through regulatory submissions. Additional years of experience will be required for the more senior roles of Senior Project Leader (SPM), Associate Project Director and Project Director.

To excel in this role, flexibility, problem solving capabilities and strategic vision are qualities that propel our Project Leadership team member’s growth. In addition, you need to be detailed-oriented, computer proficient and possess superior interpersonal and organizational skills.

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