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 Student Contract]
Job ID R0000043393 Berlin, Land Berlin, GermanyWe are offering an internship opportunity as a Quality Control Assistant in our Early Phase Clinical Trials Unit in Berlin.
You'll be at the heart of our operations—meticulously reviewing clinical documentation, validating data entry, and ensuring every study meets the highest standards of Good Clinical Practice (GCP). This is your opportunity to gain hands-on experience in a dynamic, fast-paced clinical research environment while making a real impact on patient safety and data quality.
This is a great opportunity for students to gain experience in the world of clinical trials.
This is a 12-month, part-time contract: 16 hours per week (+25%).
The Role
You'll be responsible for:
- Reviewing and validating clinical documentation (Informed Consent Forms, assessment data, adverse events)
- Ensuring data accuracy, completeness, and compliance with GCP and Good Documentation Practice (GDocP) guidelines
- Performing quality checks on source data and electronic/paper Case Report Forms (CRFs)
- Supporting the team with data entry and database management using ClinBase®
- Collaborating with study teams to maintain the highest standards of data integrity.
What We're Looking For
- You are currently enrolled in a medical or scientific university program
- Strong attention to detail and commitment to accuracy
- Excellent communication and organizational skills
- Proficiency with Windows Office and ability to quickly learn new systems
- Background in a medical or scientific field (preferred)
- Experience with data validation, transcription, or processing (a plus!)
- Fluent skills in German and English (written and spoken).
What We Offer
- 12-month part-time contract: 16 hours per week (with flexibility for up to 25% additional hours)
- Real-world experience in clinical trials and regulatory compliance
- Mentorship from experienced clinical research professionals
- A supportive team environment where your contributions matter
- Valuable skills and credentials for your future career in clinical research.
Recently Viewed Jobs
You have not recently viewed any jobs
View all jobs