Supervisor, Operations Pharmacology
Charles River Laboratories
Shrewsbury, MA 01545
Date Acquired : 2/14/2019 11:08:29 PM
Date Updated : 6/11/2019 11:23:29 PM
Supervisor, Operations Pharmacology
Req ID #: 42272
Shrewsbury, MA, US, 01545
For 70 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, well help you build a career that you can feel passionate about.
We are seeking an experiencedSupervisor, Operations Pharmacologyfor ourSafety Assessmentsite located inShrewsbury, MA.
TheSupervisor, Operations Pharmacologywill supervise, schedule, and coordinate study related activities of research technical staff to ensure compliance with the protocol and applicable SOPs. They will also develop work schedules, coordinate assignments and supervise the staff for assigned tasks and projects. They will provide direct daily supervision and review work of assigned departmental employees to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, and procedures [SOPs, safety procedures and bio-safety protocols.]
The following are minimum requirements related to theSupervisor, Operations Pharmacologyposition:
+ Education: Bachelors degree (B.A./B.S.) or equivalent in life sciences or related discipline.
+ Experience: 2-4 years related experience in a GLP environment and experience with research and investigative procedures, techniques and literature.
+ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
+ Certification/Licensure:ALAT required, LAT preferred.
+ Other:Ability to organize, prioritize work and meet deadlines. Computer literacy including word processing and spreadsheet software. Ability to successfully lead a team. Demonstrate strong verbal and written communication skills.
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 120 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 13,000 employees within 80 facilities in 23 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients 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 peoples 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 supported the development of 80% of the drugs approved by the FDA in 2017.
For more information, please visitwww.criver.com.
Equal Employment Opportunity
Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet