Quality Control Assistant [Temporary Student Contract]

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

We 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.