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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Project Manager - EP
Job ID R0000030178 Harrow, England, United KingdomAn exciting opportunity for a Project Manager (PM) to joining the project management team at our Early Phase (EP) Unit in Harrow. In this role as a PM, you will lead the Parexel and Sponsor teams by combining a depth of clinical research experience and project management skills with insight into sponsor pressures and an ability to develop the right solution for each sponsor.
We are looking for an experience Project Manager who can lead Parexel and Sponsor teams by combining clinical research experience and project management skills to develop tailored solutions for sponsors. The role involves ensuring operational excellence and successful execution of clinical trials, delivering projects on time, within budget, and to the highest quality standards.
Key Accountabilities:
- Provides overall leadership of Early Phase clinical trials or programs.
- Owns the sponsor relationship, provides a central point of study contact, and ensures proactive communication with sponsors and internal groups
- Ensures the project teams achieve operational excellence and successful execution of the clinical operations and logistical strategy.
- Manages study start-up activities, defines and plans site selection strategy, reviews project contracts and budgets, and sets up project team
- Identifies potential project risks, implements contingency plans, and keeps clients informed about risks and contingencies
- Leads administrative closeout procedures, ensures project documentation is archived, and conducts end-of-study meetings to document lessons learned
- Accountable for the financial aspects of project(s) including input into revenue recognition, milestone payments, and monthly pass-through invoices.
- Understands and ensures compliance with SOPs, contract terms, system requirements and metrics.
- Oversees PM Assistants to assure development of the project plan, team lists, and maintenance of central files /regulatory files.
Knowledge/Skills:
- An experienced PM/Associate PM or equivalent experience or related work experience in project management or related fields
- Experience as a Functional Team Leader in clinical/data management/logistics functions or proven experience in coordinating clinical trials
- Excellent presentation and speaking skills (business development experience desirable)
- Budget/Contract experience desirable
- In depth knowledge of guidelines, ICH-GCP and other applicable local and international pharmaceutical industry regulations
- Good working knowledge of MS-Office products such as Excel, Word, PowerPoint, and Project
Education:
- Bachelor’s degree in a science related field or a wealth of related work experience as a clinical research project manager.
- Or BA degree with work related experience as a clinical research project manager.
- Scientific/Medical/Pharmacology background desirable
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