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.