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.