Project Support - (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.

Are you a driven student with a passion for clinical research and data excellence? Join Parexel's dynamic Clinical Project Management team as a Project Support and gain hands-on experience in one of the world's leading clinical research organizations.

In this role, you'll support critical clinical trial operations, contribute to quality-driven processes, and work alongside experienced professionals who are committed to advancing patient care through rigorous data management and analysis.

This role is fully office-based in Berlin.

The successful candidate will have availability as follows: Students [16 hours per week (+25%) ] and Temporary Workers minimum 20 hours per week.

Key Responsibilities:
Project Support

• Assist in developing and maintaining global program tracking systems that keep complex clinical trials running smoothly
• Support the review and interpretation of statistical analysis plans and database specifications
• Contribute to project start-up activities, ensuring all essential documentation is properly organized and accessible
• Help maintain comprehensive study documentation that meets strict regulatory standards.

Statistical Programming & Quality Assurance

• Learn and apply efficient programming techniques to produce derived datasets, tables, figures, and data listings
• Participate in quality control processes to ensure all outputs meet Parexel's high corporate standards and regulatory requirements
• Assist in preparing for and participating in internal and external audits
• Develop practical skills in data integrity and validation
• Support process improvement initiatives that enhance efficiency and effectiveness.

Professional Development

• Engage in comprehensive training on clinical data management systems, electronic data capture (EDC), and clinical trial management systems (CTMS)
• Participate in mentorship opportunities and knowledge-sharing forums with experienced professionals
• Build a strong foundation for a career in clinical research

Key Requirements:

• Strong analytical mindset with basic programming knowledge and genuine eagerness to develop new skills
• Quick learner who thrives in evolving technical environments
• Meticulous attention to detail with excellent organizational abilities
• Effective time manager who can prioritize tasks and meet deadlines
• Clear communicator with strong presentation skills
• Client-focused approach with a collaborative team mindset
• Flexible and adaptable, with strong problem-solving abilities
• Proficient in written and oral English and German
• Currently pursuing a degree in statistics, computer science, mathematics, or a related discipline with a strong academic record.