Clinical Project Manager

143473
  • 110000 USD - 150000 USD
  • Plano, United States
  • Permanent

Title: Clinical Project Manager - Oncology

 

Location: Texas-based Candidates

 

Position Overview: As a Clinical Project Manager specializing in Oncology, you will play a pivotal role in overseeing the planning, implementation, and execution of clinical trials for our oncology drug development programs. You will collaborate closely with cross-functional teams to ensure the successful delivery of clinical studies while maintaining compliance with regulatory standards and timelines.

 

Key Responsibilities:

  • Lead the planning and execution of oncology clinical trials from start-up to close-out, ensuring adherence to protocol, budget, and timelines.
  • Coordinate cross-functional teams, including Clinical Operations, Data Management, Regulatory Affairs, and Medical Affairs, to drive study milestones and deliverables.
  • Oversee site selection, feasibility assessments, and investigator meetings to ensure efficient study start-up.
  • Manage vendor relationships and third-party vendors involved in clinical trial activities, including clinical research organizations (CROs), central laboratories, and imaging vendors.
  • Monitor study progress, identify risks, and implement mitigation strategies to ensure the successful execution of clinical trials.
  • Collaborate with internal stakeholders to develop study documents, including protocols, informed consent forms, and clinical study reports.
  • Contribute to the development of study budgets, track project expenses, and manage financial aspects of clinical trials.

 

Qualifications:

  • Bachelor's degree in life sciences or related field; advanced degree preferred.
  • Minimum of 2 years of experience in clinical project management, with a focus on oncology drug development.
  • Proven track record of successfully managing oncology clinical trials from start-up to close-out.
  • Strong understanding of clinical trial operations, including site management, monitoring, and regulatory requirements.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively across cross-functional teams.
  • Detail-oriented with strong organizational and problem-solving abilities.
  • Proficiency in project management tools and software applications.
  • Experience working in a fast-paced, dynamic environment within the pharmaceutical or biotechnology industry.
Amanda Blunck Senior Division Manager

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