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 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%)
This role is fully office-based in Berlin.
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.