Manager of Clinical Services Projects

2 weeks ago


Remote, Oregon, United States Revel IT Full time
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Revel IT is seeking a Clinical Services Project Manager for a remote contract position. This role involves overseeing clinical and laboratory services projects from inception to contract fulfillment, utilizing project management expertise to ensure timely delivery, budget adherence, and high levels of client satisfaction. You will facilitate collaboration across various functions to meet project deadlines.

  • Location: This is a remote based role.

Key Responsibilities:

  • Lead and manage clinical testing and laboratory services projects collaboratively, from initiation to contract completion.
  • Coordinate project timelines and activities within CDx Pharma Services, including developing project plans, establishing timelines, managing execution of cross-functional plans, and tracking progress; identify potential issues and propose solutions to address them.
  • Supervise daily operations related to sample processing and ensure accurate reporting of results.
  • Implement best practices within the clinical sciences team, promoting continuous improvement through knowledge sharing and experience exchange.
  • Facilitate and manage cross-functional collaboration to ensure project completion within established deadlines.
  • Engage with external resources, including Contract Research Organizations (CROs), site investigators, and client representatives, serving as the primary contact for Pharma and Roche clients.
  • Perform additional duties and special projects as assigned.

Qualifications:

  • A Bachelor's Degree in a relevant field or an equivalent combination of education and experience.
  • A minimum of 2 years of experience in project management or clinical trial coordination within a regulated environment, such as CRO, diagnostics, or pharmaceuticals, with an emphasis on regulated documentation.

Preferred Qualifications:

  • A Master's Degree in a relevant field and/or specialized training in Project Management or Clinical Research.
  • Experience in clinical trial management and familiarity with bio-sample management and processes in the diagnostics or pharmaceutical sectors.
  • Knowledge of standard project management methodologies (PMI).
  • Understanding of quality and regulatory processes.
  • Proficient in clinical sample processing and testing methodologies.
  • Strong skills in word processing, spreadsheets, databases, and email software (e.g., Microsoft Excel, Microsoft Word).
  • Ability to apply specialized knowledge and skills effectively, particularly in collaboration with laboratory, scientific, and medical personnel.
To Apply for this Job Click Here

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