Jobs at Parexel
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.
Clinical Assistant
Job ID R0000032746 Istanbul, Istanbul, TurkeyThe role of the Clinical Operations Assistant (COA) is to complete administrative tasks on behalf of assigned Project Clinical Team which might include tasks related to site payments, management of site supplies, trial master file, site activation, Clinical Trial Management System (CTMS), study trackers and system updates and site facing tasks to support the efficiency, accuracy, and quality of the trials.
The COA also supports all site management team members on local billable administrative tasks and assists with QC of Central files.
Skills:
• Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
• Maintain a strong knowledge and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations and applicable Parexel procedures and Client specific procedures.
• Good oral and written communication skills to internal and external customer.
• Ability to prioritize multiple tasks and achieve project timeline.
• High commitment to and performs consistently high-quality work.
• Effective problem-solving skills.
• Mentor and train less experienced staff as appropriate.
• Active participant as a process and/or platform Subject Matter Expert (SME) with minimal LM oversight.
• Fluent English and Turkish skills (oral and written).
Knowledge and Experience:
• Experience in office management in an international environment would be advisable.
Education:
• Relevant qualification or equivalent experience required.
• High school diploma – ideally degree in life science or other related background – preferred.
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