Overview
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At Charles River, we are passionate about improving the quality of people's lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.
Job Summary
Do you have significant expertise in Toxicology and Pathology, and a passion for line management and leadership?
Would you like to apply your expertise to lead and direct a multi-disciplinary function, forming and implementing innovative strategy effectively?
Have you got the desire to improve health and lives?
Charles River Laboratories are excited to be recruiting for a Senior Director of Toxicology and Pathology for our Safety Assessment site in Tranent, Edinburgh on a full time, permanent basis reporting to the site\'s General Manager.
The Senior Director of Toxicology and Pathology will be site based and you will join as a key part of the Site Leadership Team of the overall Edinburgh site. With experienced managers reporting directly to you, you will lead a team of over 70 toxicology and pathology professionals working across the disciplines of toxicology and pathology, including General Toxicology studies, Safety Pharmacology, Inhalation, Developmental and Reproductive Toxicology and In Vitro Toxicology, all who are responsible for the study management and reporting of safety assessment studies for Charles River.
This is a fantastic opportunity for a highly experienced toxicologist or pathologist looking for their next step in management and to lead the development and implementation of the strategic and tactical plan for this division.
About the opportunity
As an expert in this field, you will utilise a deep understanding of highly regulated safety assessment studies within the pharmaceutical industry to anticipate, shape and respond to the needs of internal and external stakeholders to deliver a successful outcome for all parties.
Responsibilities
* Set the scientific direction and standards of the division. This will include meeting with clients, representing the company at scientific meetings or on industry working parties, liaising with peers at other global Charles River sites.
* Provide independence of thought to suggest fresh approaches and improvements at the Edinburgh facility and with global colleagues.
* Act as the Edinburgh Leadership Team representative for Toxicology and Pathology and be line manager for the Directors and other managers in the Toxicology and Pathology Groups, including recruitment and expenditure reviews, sales plans, and expense approvals.
* Liaise with the Edinburgh Senior Leadership Team to ensure consistent decision-making and coordinate activities across the Edinburgh site.
* Responsible for testing facility management duties as delegated by the General Manager regarding Edinburgh toxicology and pathology operations.
* Ensure that all sales and marketing activity for the Toxicology and Pathology Groups is planned and implemented and reviewed regularly to align with divisional and corporate objectives.
* Assist the General Manager and Finance Director to review and decide on budgets for the Toxicology Group departments and monitor performance against targets.
* Ensure the conduct and completion of studies in the Toxicology and Pathology Groups to a high-quality standard using sound scientific methods and proper control procedures.
* Achieve effective use of staff and resources, motivate the team, ensure job satisfaction, and deliver high-quality work while prioritising customer care.
* Prepare long-range plans for the Toxicology and Pathology Groups and determine future areas of activity.
* Maintain constructive relationships between the departments within Safety Assessment and related divisions.
* As a member of the Leadership Team, contribute to the overall management and ongoing success of the site.
What We Offer You
* A comprehensive benefits package from day one, including a competitive pension contribution, private medical for you (and can include family members), bonus and more
* Global opportunities and strong career progression
* Opportunity to work on varied projects and liaise globally and nationally with other business areas
* Make a difference to health and wellbeing
* Continued career growth
* Life Assurance
* Well-being support and initiatives
Profile and Requirements
About you
You will be a graduate most likely with a higher degree; a relevant qualification in toxicology or pathology is highly desirable. You will have shown commitment to personal professional development. Professional memberships, certification and qualification in relevant topics in toxicology, pathology and/or management are highly desired.
Already highly experienced in regulatory safety assessment, you will have a wide knowledge of the pharmaceutical and/or agrochemical industry sectors and a track record demonstrating the ability to influence others to deliver excellent execution.
Skills and Experience:• Educated to a higher degree within a relevant discipline area (toxicology or pathology). • Significant industrial experience working on safety assessment studies from a toxicology or pathology perspective is essential; CRO/Biotech experience is preferred. • Demonstrable line management experience, particularly within a matrix function across different scientific disciplines; experience managing managers is essential. • Proven business and commercial acumen with experience liaising with clients and stakeholders.
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 regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth journey to market. Each year approximately 300 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 GLP and non-GLP, to support clients from target identification through preclinical development. Charles River also provides services to support clinical laboratory testing needs and manufacturing activities. This broad portfolio enables clients to create a more flexible drug development model, reducing costs and increasing speed to market.
With over 20,000 employees within 110 facilities in 20 countries, we coordinate worldwide resources and apply multidisciplinary perspectives to resolve client challenges. Our client base includes global pharmaceutical and biotechnology companies, government agencies, hospitals and academic institutions.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, science, and purpose guide our work and help improve health and well-being globally. We have proudly supported the development of 86% of FDA-approved drugs in 2021.
We recognize and recruit all talent and are committed to diversity and inclusion. For more information, please visit the company website.
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