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.