Principal Business Process Leader, Scientific Data Organization

7 days ago


Sheffield, Sheffield, United Kingdom Parexel Full time

About This Role

Parexel is seeking a highly skilled and experienced Principal Business Process Leader to join our Scientific Data Organization team. As a key member of our organization, you will play a critical role in leading cross-functional initiatives and projects that drive business growth and improvement.

Key Responsibilities

  • Lead and facilitate internal projects and initiatives that leverage best-in-class design, expertise, and technology to drive business outcomes.
  • Develop and implement infrastructure development across Real-World Evidence (RWE) functions, including tracking tools, processes, and toolkits, capacity management, and metrics development.
  • Work independently to build understanding, delivery frameworks, and expert teams to develop RWD and technology-enabled solutions for RWE projects.
  • Manage the setup of RWE/SDO-centered or supported components of initiative delivery.
  • Lead the development of initiative plan elements, including roles and responsibilities, project plans, communication plans, and risk analysis.
  • Facilitate the definition, input, and approval of SDO budget in relation to SDO resource, data source procurement, and/or SDO-covered technology components for any given initiative.
  • Lead and document discussions during all phases of an initiative, ensuring the RWE/SDO scope of the initiative is well understood by the SDO/business partner, initiative team, and all supporting functions.
  • Ensure initiative management tools are in place to support collective initiative management across functions and to easily support SDO and BO oversight.
  • Ensure SDO-initiative elements are completed within schedule and according to budget specifications.
  • Ensure SDO-initiative elements are progressing according to quality standards, SOPs, and/or other guidelines to fulfill local regulations as applicable.
  • Set up and use initiative plans as management tools to record, measure, and manage progress.
  • Proactively communicate with the SDO/business partner team to ensure they have all the information required on progress and status (risk analyses, contingency plans, technical information, significant changes of any kind, etc.).
  • Work with BP's/SDO internal teams and QM to oversee the development, review, approval, and implementation of any controlled processes developed on an initiative as required.

Requirements

  • Bachelor's degree in life science as a minimum.
  • Fluent English.
  • Late-phase/RWE/RWD-oriented clinical research experience in both interventional and observational study contexts with significant global project management experience as project manager or clinical leader or equivalent.
  • Experience in developing and delivering operational models in clinical research.
  • Potential exposure to and experience in setting up and leading cross-functional initiatives.
  • Familiarity with the regulatory, data privacy, and data security landscape for interventional and non-interventional Real-World Evidence projects with and without usage of Real-World Data.
  • Organized with excellent oral presentation and written communication skills.
  • Strong customer focus (internal and external).
  • Experienced in technical and operational project planning and management.


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