Analytical Study Director

Location:

Veszprem – Hungary

Salary:

Competitive

Type:

Permanent

Main Industry:

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Other Industries & Skills: 

Education & Training, Engineering, Health, Nursing & Social Services, Information Technology, Management & Executive, Science

Advertiser:

Charles River Laboratories, Inc.

Job ID:

131675238

Posted On: 

12 March 2025

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.

Analytical 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:

-Key role is management of physico-chemical studies (e.g. hazard parameters or basic property) and analytical method development and validation of substances used in preclinical studies or regulatory toxicity studies
-Study set-up, study plan, study conduct and supervision
-Coordination of the study team
-Scheduling of work for the group to ensure maximum use of facility
-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.
-Responsible for contributing as Contributing Scientist or Principal Investigator to the conduct the delegated phase of a study according to the study plan (including sunsequent amendments) and should ensure that the applied procedures are compliance with the Study requirements and guidelines
-Responsble 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
 

Key Required Skills and Education:

-Minimum of Bachelor level education in chemistry, especially in analytical chemistry or similar 
-1-3 years of professional experience (preferred, but not mandatory)
-Basic or high level experience in working with any chromatography (HPLC, GC, or MS techniques)
-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 (formula, calculation), Powerpoint, any chromatographic software’s, any statistical software’s
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.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, a member of our Human Resources team by sending an ssage to crrecruitment_UScrl. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, criver.

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