When our values align, there's no limit to what we can achieve.
Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the world transform scientific discoveries into new treatments. We believe in our values.
We are currently looking to recruit an experienced professional to lead project delivery and oversight of our projects on a global level. This position is available in the following EMEA locations, and we offer fully remote (country stipulated), hybrid, or office-based working.
As a Senior Project Leader, you will actively lead the Parexel and client teams by combining your deep clinical research experience with insight into client pressures in order to develop the right solution for the client.
You will provide overall cross-functional leadership of our clinical trials and studies as well as the project teams to achieve operational excellence and deliver projects on time, to budget, with the highest quality, and compliant with ICH GCP to meet client expectations.
Key Accountabilities:Develop and maintain a formal project plan with all key milestones, budgets, and resources assigned to specific tasks and outcomes.Identify potential project risks and implement contingency plans, mitigate actual risks with team members, and keep the client informed about risks and contingencies.Establish quality standards for the project that drive individual and team commitment to quality.Own the client relationship at a study level and be responsible for client communication ensuring high client satisfaction.Manage the project according to budget with revenue recognition and forecasting, including resource management and pass-through management (review, regular reconciliation, and forecasting).Enable all stakeholders to achieve successful study completion while maintaining high client satisfaction.Represent Project Leadership Function in external client meetings and presentations such as Bid Pursuit Meetings, Investigator Meetings, or others as required.May include non-billable work such as SOP review and lead or contribute to other organizational initiatives.Education: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: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 be able to prioritize workload with high attention to detail.Ability to work in a matrix environment and to 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, and 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.Strong command of written and spoken English language is essential. An additional language is a benefit.Familiarity with standard business and eClinical systems used in Clinical Research is desirable.Solid clinical knowledge and understanding of clinical research and protocol design.In return, we will be able to offer you 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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