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.
Quality Control Assistant [Temporary Contract]
Job ID R0000040074 Berlin, Land Berlin, GermanyThe Quality Control Assistant is responsible for quality control, transcription and clarification of data collected during study conduct within the Early Phase Clinical Unit. This role ensures data accuracy, completeness, and compliance with Good Clinical Practice (GCP) guidelines and study protocols through systematic review of clinical documentation, and accurate data entry into electronic and paper Case Report Forms.
The successful candidate will have availability as follows; Students [16 hours per week (+25%) ] and Temporary Workers minimum 20 hours per week.
Key Accountabilities:
Check Informed Consent Forms for completeness and compliance
Corrections done according to GCP and Good Documentation Practice (GDocP) guidelines
Check In/ Exclusion criteria according to protocol requirements
Control of assessment performance according to protocol specifications
Control of source data in timely manner to ensure accuracy and completeness
Check of data regarding completion and plausibility
Check of source data against database for consistency and accuracy
Control of Adverse Event / Concomitant Medication documentation
Data entry from ClinBase® and source data to paper- / e-CRF
Check of ClinBase® and source data versus paper- / e-CRF entries
Other tasks in the opinion of the manager and as required by the EPCU Operations
Skills:
English language knowledge
Communication skills
Computer skills (Windows Office)
Knowledge and Experience:
Experience in data transcription, data validation or data processing preferred
Education:
Medical or Scientific University education preferred
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