Quality Control Assistant [Temporary Student Contract]

Parexel; Berlin; Presencial; EUR 10.000 - 15.000; A tiempo parcial

Ventajas ofrecidas por este puesto de trabajo

Mentorship from experienced clinical研究

Descripción de la vacante

Parexel in Berlin offers an internship as a Quality Control Assistant in our Early Phase Clinical Trials Unit. You will review clinical documentation, validate data entry, and ensure studies meet GCP standards while gaining hands-on experience in a fast-paced clinical research environment.

This 12-month, part-time internship (16 hours/week, with up to 25% extra hours) is ideal for students seeking real-world exposure to regulatory compliance and data integrity in trials.

Formación

• Enrolled in a medical or scientific university program.
• Strong attention to detail and accuracy.
• Excellent communication and organizational skills.
• Fluent German and English (written and spoken).
• Proficiency with Windows Office; ability to quickly learn new systems.

Responsabilidades

• Reviewing and validating clinical documentation (ICFs, assessment data, AE) and ensuring data quality.
• Ensuring data accuracy, completeness and GCP/GDocP compliance.
• Performing quality checks on source data and CRFs (electronic/paper).
• Assisting with data entry and database management using ClinBase®.
• Collaborating with study teams to maintain data integrity.

Conocimientos

Attention to detail

Fluent German & English

Communication skills

Organizational skills

Quick learner

Educación

Enrollment in medical or scientific university program

Herramientas

Microsoft Office

ClinBase

Descripción del empleo

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.