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Parexel

Project Manager, Early Phase

Posted 2 months ago
2-5 years experience
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AI Summary

The Project Manager is responsible for leading early-phase clinical trials from initiation to close-out, ensuring they are completed within budget and schedule. This includes managing sponsor relationships, overseeing study start-up, and mitigating project risks.

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.

Key Accountabilities:

Communication and Sponsor Liaison

  • Own the sponsor relationship and manage sponsor communication.
  • Serve as the central point of contact and escalation for functional teams.
  • Proactively communicate project progress, risks, and solutions to sponsors and internal teams.
  • Lead regular meetings with sponsors and project teams to ensure objectives are met.

Pre-award Activities

  • Review relevant materials and attend strategy meetings.
  • Prepare for Bid Defense and develop project management strategies.
  • Attend Bid Defense and handover meetings.

Project Planning & Initiation

  • Manage study start-up activities and ensure best practices are implemented.
  • Oversee site selection strategy and review project contracts and budgets.
  • Set up project teams and systems, and manage IRB/EC and RA approval processes.
  • Lead internal and sponsor kick-off meetings and ensure team understanding of project scope and expectations.

Project Implementation, Control & Evaluation

  • Lead projects to completion within budget and schedule, ensuring contract specifications are met.
  • Provide performance feedback and ensure project tracking using CTMS.
  • Monitor study timelines, recruitment, retention, and data cleaning.
  • Prepare for audits/inspections and manage project budgets.

Project Close-out

  • Oversee administrative closeout procedures and ensure project documentation is archived.
  • Lead end-of-study meetings to document lessons learned.

Risk Management

  • Identify potential project risks and implement contingency plans.
  • Mitigate risks and keep clients informed throughout the study life cycle.

Administrative Tasks

  • Contribute to SOP development and provide oversight and training to Associate PMs and Project Assistants.

Skills:

  • Leadership skills to lead virtual teams across locations and cultures.
  • Negotiation and influence skills to achieve results.
  • Decision-making skills in ambiguous situations.
  • Problem-solving and root cause analysis skills.
  • Excellent interpersonal, oral, and written communication skills.
  • Time management and organizational skills.
  • Strategic thinking and financial management skills.

Knowledge and Experience:

  • 2 years of Project Management experience with Parexel or 3 to 5 years in related fields.
  • Experience as a Functional Team Leader or in coordinating clinical trials.
  • Knowledge of ICH-GCP and pharmaceutical industry regulations.
  • Proficiency in MS-Office products.

Education:

  • Bachelor’s degree in a science-related field or equivalent work experience.
  • Advanced degree preferred.
  • Additional business degree or PMP certification is an advantage.
  • Scientific/Medical/Pharmacology background is an advantage.

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