Study Director

Study Director

The Study Director responsible for the scientific conduct of a study and can confirm the compliance of the study. Represents the single point of study control and has overall responsibility for the scientific and technical conduct of the study. Oversight of data collection, interpretation, analysis, documnetation and reporting of results; and the derivation of study conclusions. In order to do so the Study Director provides leadership, communication, support & assistance.

Your tasks:

• Respective specialities: ecotoxicology, in vitro toxicology, genetic toxicology
• Key role in management of preclinical studies or regulatory toxicity studies
• Study set- up, study plan, study conduct and supervision
• Oversight of data collection, interpretation, analysis, documentation, and reporting of results; and the derivation, of study conclusions
• Responsible for the conduct of the good technical aspects of the study phase and/or the data evaluation, reporting and sharing any study related event with the responsible Study Director during the delegated phase
• Coordination of the study team
• Review of the study documentation, data evaluation, study report
• Close collaboration with internal departments and external partners
• Work in compliance with applicable GLP, ISO and SOPs.

Key Required Skills and Education:

• Minimum of Bachelor level education in biology, veterinary medicine, agricultural or similar
• 1-3 years of professional experience (preferred, but not mandatory)
• Good verbal and written communication skills and superior customer service skills
• High degree of self-motivation with effective organizational and time management skills
• High level spoken and written English required
• Computer skills including Word, EXCEL, Powerpoint

The pay range for this position is 670.000 – 850.000 [HUF]. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications and location if applicable.

Location: Veszprém

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

About Safety Assessment

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

About Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.