Job Description
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.