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Sr. Director Laboratory Sciences
| Company | Charles River Laboratories |
| Address | , Ashland, Oh |
| Employment type | |
| Salary | $170,000 - $230,000 a year |
| Expires | 2023-06-18 |
| Posted at | 1 year ago |
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.
Job Summary
Direct the science and business involved in the conduct, direction and execution of Laboratory Sciences operations and studies. Provide scientific direction, oversight, and guidance to staff. Maintain and implement efficient processes and procedures to provide high quality standards of study design and timely reporting. Continue to build preclinical and clinical bioanalysis and biomarkers capabilities in an effort to expand the client base. Serve as primary expert for Laboratory Sciences within the scientific community presenting and speaking at meetings and interacting with new and perspective clients. Keep abreast and maintain a broad knowledge of state-of-the art principles and theories.
- Monitor performance of direct reports. Provide regular coaching and counseling.
- Be seen as a recognized expert in the areas of scientific expertise in Laboratory Sciences. Deliver scientific presentations lead and/or participate in industry groups and participate in the discussions and writing of scientific guidance for industry.
- Identify key regulatory requirements and guidelines that pertain to preclinical and clinical testing and specialty services that we provide.
- Lead interactions for Ashland Laboratory Sciences with Sponsors, consultants, and other outside contacts; interact with government representatives and Sponsors when site visits are conducted.
- Oversee and ensure report timelines are maintained and perform quality assessments to ensure high quality study design and timely reporting.
- Develop and recommend departmental budget. Approve budget and expenses of subordinates.
- Perform testing facility management duties for the site as delegated by DSA senior management.
- Ensure that management training and development needs are identified and programs initiated.
- Represent the organization to industry groups, key customers, representatives of government and regulatory agencies and the general public.
- Evaluate opportunities for new technology, and implement new scientific initiatives to add additional or expanded services in Laboratory Sciences.
- Ensure departmental policies, practices and procedures adhere to GLP/FDA regulations as they relate to the conduct of preclinical studies. Establish new policies and practices to ensure compliance with all applicable regulations and corporate policies.
- Ensure coordination of study bids, study design and conduct, protocol review, consultant interactions, staffing needs, analysis, and reporting of Laboratory Sciences studies.
- Provide senior level review of protocols, reports and related documents for appropriate scientific content and interpretation in collaboration with other senior staff.
- Bear responsibility for the Lab Sciences P&L in Ashland including reporting, planning, forecasting as required.
- Lead and promote new business development for Laboratory Sciences in Ashland as the primary scientific expert for existing and new clients. Continue to build preclinical and clinical bioanalysis and biomarkers capabilities in an effort to expand the client base.
- Contribute to recruitment of research scientists and support staff. Contribute to overall facility management Interview and select qualified exempt-level departmental personnel.
Job Qualifications
Education: Master’s degree in chemistry, immunology, biochemistry, or a related scientific discipline required. PhD preferred.
Experience: 10 years relevant laboratory experience in a contract research organization (CRO), biotechnology, or pharmaceutical environment, working to Good Laboratory Practice (GLP) standards. 5 years management experience, including staff management and development, and financial responsibility including budgets. An equivalent combination of education and experience may be accepted as a satisfactory substitute.
Other: Management and problem solving skills. Demonstrated abilities in analytical, quantitative, and critical thinking. Ability to handle multiple projects, meet deadlines and make executive level decisions. Detail oriented, flexible with the ability to work well in a team-oriented environment. Proven ability to work in a dynamic, deadline driven environment. Proficient project management, presentation, and communication skills. Proficient with computers and standard application software.
The pay range for this position is $170K - $230K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
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.
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