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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.
Site Start up EUCTR II
Job ID R0000042680 Hyderabad, Telangana, IndiaSite Start Up EUCTR II
- Responsible for planning and submitting the complex EUCTR submission i.e. large phase II and III trials with multiple countries and sites.
Job Requirements: In addition to the core duties outlined, the following qualifications are required for the Site Start Up EUCTR II
- Interpersonal & leadership skills
- Ability to understand and implement the operational strategic direction and guidance for respective clinical studies
- A data driven approach to planning, executing, and problem solving
- Effective communication skills via verbal, written and presentation abilities
- Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization
- Ability to build productive study teams collaborations
- Vendor management experience
- Basic proficiency in trial management systems (CTMS, TMF) and MS applications including (but not limited to) Project, PowerPoint, Word, Excel
- Experience in the clinical drug development process, including study start-up
- Knowledge of ICH/GCP, EUCTR and IVDR regulatory guidelines
- Basic project management skills, cross-functional team interaction and organizational skills
- May require up to 25% travel
- Bachelor’s degree and 3-4 years of relevant experience.
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