Analytical Study Director

• Professional preparation of the study plan(s); Managing amendments
• Managing GLP (OECD) and internal SOPs; supporting audits
• Monitoring the completeness and accuracy of raw data (ALCOA+); Coordination of evaluation, reporting, archiving
• Verify the availability of resources, test systems, and test materials
• Client contact, organizing/leading professional consultations and visits; providing scientific inputs for tendering
• Professional supervision of the use/calibration/qualification of computer systems (CSV) and laboratory equipment

• Higher education in natural sciences (preferred: MSc/PhD)
• Multiple years of experience as a study leader/study coordinator in a GLP environment is an advantage
• Confident oral and written English skills
• Experienced documentation and reporting; risk management and decision-making skills
• Excellent cooperation with QA, technical and business areas;
• Customer-centric communication

• In-depth knowledge of GLP/OECD guidelines; audit experience
• Test design, change/deviation management in practice
• CSV basics; Proficiency in SZME preparation

• Competitive income
• Varied, high-impact projects
• Helpful, professionally strong team
• Development and further training opportunities (internal/external trainings)

Our company, Charles River Laboratories Hungary is a USA based CRO. Charles River Laboratories has been supporting the research, development and safe production of new drug therapies for nearly 70 years. Through our work, we contribute to improving the health and well-being of people around the world. The expertise of our team plays a valuable role in the success of the company. If you apply to us, we will help you develop a career that you can really commit to.