Senior Project Manager

hace 1 semana


Alcobendas, Madrid, España Parexel A tiempo completo

About the Role:

Parexel is a leading biopharmaceutical services company that improves the world's health by transforming scientific discoveries into new treatments. We are seeking an experienced professional to lead project delivery and oversight of our projects on a global level.

Key Responsibilities:

  1. Develop and maintain a formal project plan with all key milestones, budgets, and resources assigned to specific tasks and outcomes.
  2. Identify potential project risks and implement contingency plans, mitigate actual risks with team members, and keep clients informed about risks and contingencies.
  3. Establish quality standards for the project that drive individual and team commitment to quality.
  4. Own the client relationship at a study level and be responsible for client communication ensuring high client satisfaction.
  5. Manage the project according to budget with revenue recognition and forecasting, including resource management and pass-through management (review, regular reconciliation, and forecasting).
  6. Enable all stakeholders to achieve successful study completion while maintaining high client satisfaction.
  7. Represent the Project Leadership Function in external client meetings and presentations such as Bid Pursuit Meetings, Investigator Meetings, or others as required.
  8. May include non-billable work such as SOP review and lead or contribute to other organizational initiatives.

Requirements:

  • Bachelor's degree or equivalent level of education (Science or Medical related field preferred) or proven substantial clinical project management experience.
  • Advanced degree desirable.

Skills and Qualifications:

  • Ability to take a proactive, solutions-based approach.
  • Critical thinking & problem-solving.
  • Excellent interpersonal, verbal, and written communication skills.
  • Highly accountable with a strong client focus.
  • A flexible attitude with respect to assignments and new learning.
  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with high attention to detail.
  • Ability to work in a matrix environment and value the importance of teamwork and collaboration.
  • Basic understanding of all aspects of the project life cycle.
  • Ability to work independently with oversight guidance.
  • Proficient in Microsoft Excel, PowerPoint, Word, and project planning software.

Knowledge and Experience:

  • Strong previous CRO experience and understanding with demonstrable skills are essential.
  • In-depth knowledge in any therapeutic areas (TA's) is welcome. There is a strong preference for a combination of the following areas due to our current resource needs: therapeutic expertise.
  • Strong command of written and spoken English is essential. An additional language is a benefit.
  • Previous involvement in clinical research is required.
  • Strong communication and interpersonal skills are essential.
  • Applications from candidates with pharma experience may also be considered.
  • Familiarity with standard business and eClinical systems used in Clinical Research is desirable.
  • Knowledge of ICH and GCP regulations in relevant geographies.
  • Solid clinical knowledge and understanding of clinical research and protocol design.

What We Offer:

Parexel offers a structured career pathway and development within the role, including awareness and understanding of the industry. Your hard work will be rewarded with a competitive salary, bonus, and a benefits package including holiday, pension, and other leading-edge benefits that you would expect with a company of this type.



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