sr investigator jobs

Near tranent, scotland
5Jobs Found

5 jobs found for sr investigator jobs Near tranent, scotland

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Health & Safety Manger

Charles River Laboratories

Tranent
1 day ago
Tranent
1 day ago
Health & Safety Manger
Req ID: 97480
Location:
Tranent, GB, EH33 2NE
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, we’ll help you build a career that you can feel passionate about.
Job Summary
At our world class facility in Elphinstone, Tranent (close to Edinburgh), our Health & Safety Department currently has an exciting career opportunity for aHealth & Safety Manger.
Department Information
The Health and Safety department encompasses a wide variety of health and safety activities including, updating procedures, training, incident management, auditing and risk assessment. The main hazards on site are associated with COSHH (chemical and biological), manual handling, ergonomics/work station assessment and the use of radio-chemicals. There are also some unique operational process hazards as well as the more standard workplace safety considerations. The Health and Safety department currently provides support across four sites although the role will be based within the Elphinstone Research Centre site.
Key Responsibilities:
+ Management of the health and safety department
+ Management of incident reporting process
+ Advise and support departmental health and safety audits
+ Advise and support departmental COSHH assessments
+ Advise and support departmental risk assessments
+ Carry out health and safety training
+ Manage health and safety contractors
+ Chair management health and safety meetings and projects
+ Produce and communicate safety KPIs to senior site management
+ Provision of support, advice and monitoring of matters relating to Health and Safety to all levels of staff
+ Responsible for radiochemical use reporting and regulatory compliance requirements to SEPA
+ Liaise with and report to HSE as appropriate
Applicants should have:
+ A minimum of NEBOSH Certificate
+ Excellent influencing skills and enthusiasm for creating/maintaining a positive health and safety culture by application of continuous improvement
+ Proven experience of
+ Risk Assessments
+ Incident reporting/ investigation
+ Safety auditing
+ COSHH
+ A good understanding of health and safety legislation and its application within the workplace together with some practical work experience, ideally gained in a scientific, healthcare or engineering context.
+ Computer literacy is essential (competency of MS Office) and you must be capable of working on your own initiative.
+ You must be flexible, detail conscious and well organised
Salary for this position with be dependant on the candidates skills and experience.
The closing date for this vacancy is Friday, 12 March 2021.
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 17,000 employees within 90 facilities in 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. And in 2019, revenue increased to $2.62 billion.
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 supported the development of ~85% of the drugs approved by the FDA in 2019.
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CRA II & Senior Clinical Research Associates - CRO - Oncology

Precision Medicine Group

Edinburgh, Scotland
6 days ago
Edinburgh, Scotland
6 days ago

Precision for Medicine, Oncology and Rare Disease is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

About you:

  • You are calm, thoughtful, and responsive when things don’t go as planned.
  • You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
  • You find quick and creative ways of overcoming difficulties.
  • You have an impeccable eye for detail.
  • You identify potential study risks and propose solutions on how to mitigate them.
  • You take responsibility in the quality and outcomes of your work.
  • You are adept at handling conflict by using tried and true resolution strategies.

How we will keep you busy and support your growth:

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope. You will also have the opportunity to train and mentor junior staff members. You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.

Qualifications:

Minimum Required:

  • 4-year college degree or equivalent experience

Other Required:

  • CRA experience within the CRO or pharmaceutical industry; 2+ years for a CRA II and 3+ years for Senior CRAs
  • Oncology experience
  • Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)

Preferred:

  • Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
  • Two+ years of oncology experience
  • Study start up activities experience
  • For Senior CRAs, understanding of financial management

Precision for Medicine, Oncology & Rare Disease is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.

We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

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Senior Site Reliability Engineer

Zonal Retail Data Systems Limited

Edinburgh, Scotland
30+ days ago
Edinburgh, Scotland
30+ days ago

The Zonal group are one of the UK’s largest technology providers to the hospitality industry. Our products are used by over 11,000 pubs, restaurants, and hotels.  Customers include national brands like Pizza Express, JD Wetherspoons and All Bar One.
We provide our customers with the solutions they need to make their business a success.  These solutions include mobile apps for ordering and web apps for engaging with consumers either through loyalty or reservations. By linking these solutions to Zonal’s EPoS (till) system, we help hospitality brands to understand their customers’ behaviour and preferences, enabling them to excel in an increasingly competitive market.  

If you have booked a table or hotel room, ordered, and paid for food and drinks, received loyalty offers, or downloaded your favourite hang out’s app, you will likely have used a Zonal product. 

We are a family business with Scottish roots. We operate from our modern head office in Edinburgh to our Marketing Technologies Division in Staffordshire, or our Innovation Centre in Abingdon and hotel management solutions base in Cardiff.


What you’ll do

This role sits within the Zonal Managed Services team and is part of the wider Zonal Technical Services business unit. Our suite of SaaS, distributed systems and product integrations help our customers run their critical business operations and provide their customers in turn with industry leading hospitality technology products.  You’ll play a key role in the formation of a new area within Zonal: our Production Operations (ProdOps) team that aims to drive operational excellence and customer focus into the operation of our SaaS hosted application suite.

As a Senior Site Reliability Engineer, you’ll combine your software and systems engineering expertise in coding, system design, integration, deployment and ongoing maintenance to help build and run our industry leading SaaS solution. You will help build a new key Site Reliability Engineering (SRE) function within Zonal, implementing best practice monitoring, processes and tooling focussed on uptime, performance, and reduction of toil. You will work closely with engineering teams in Development and Platform Delivery (Networks, DBA, and Infrastructure) to uphold contracted Service Level Objectives (SLOs).  You will be tasked with ensuring our internal and externally available systems have reliability, and uptime appropriate to user’s needs.

The makeup of our systems is changing rapidly, and you’ll play a key part in helping us drive this forward.  We’re moving towards a modern DevOps landscape with technologies like Docker, IaC and microservices.  Initially we are working with our own hosted data centre infrastructure technology however, you’ll play a key role in our drive towards a future hybrid public-cloud position.

You will contribute towards driving an organisational change into Zonal focussing on the core tenants of Site Reliability Engineering, namely the availability, latency, performance, efficiency, change management, monitoring, emergency response, and capacity planning of our SaaS service(s).

You and your team will:

  • Build strong, collaborative relationships acting as the glue between in-house customer facing support and delivery teams, product management, and platform engineering (R&D) teams
  • Create frameworks to continually improve:
    • Observability through logging, monitoring, and alerting
    • Capacity analytics and demand management
    • Dashboards, internal and external status pages
    • CI / CD pipelines, release processes
    • Automation of manual processes, tooling and IaC including security checks and break-glass procedures
    • Ownership of some cross-cutting implementation like logs / metrics infrastructure
    • Team processes, driving technical debt down
    • Triage, response, and recovery times
    • Disaster Recovery models and planning
  • Reduce toil (work that is largely manual, repetitive, automatable, tactical, devoid of enduring value, and that scales linearly as our services grow), maximising engineering capacity 
  • Bring expertise and a streetwise perspective to problem solving, reduction of complexity and reliability patterns
  • Participate in On-Call cover and Incident Response
  • Play a key role in change management and delivery pipeline into production ensuring safety, predictability, repeatability, and auditability of all build and deploy processes
  • Proactively manage delivery of key SLOs covering Detection / early warning and self-healing
  • Own all monitoring and alerting applications, services and infrastructure
  • Act as key stakeholders in the technical debt reduction of our Products by contributing towards the Tech Debt backlogs for our R&D teams


Who you are

You will have a background in deploying, managing, and operating mission critical distributed SaaS systems having spent at least some of your career as a member of a fast-paced product engineering, web operations and/or platform delivery team.  Ideally you will have a demonstrable track record of operating systems in hybrid datacentre/cloud infrastructures.

When things go wrong – and they will – we want to know about the problem before our users, so will need your deep understanding of modern monitoring and toolsets for identification, investigation, and remediation.

  • A self-starter with a passion for technology and problem solving, with excellent analytical skills who thrives in a fast-paced autonomous environment leading from the front
  • A champion of resilience, consistency, security, and monitoring 
  • Solid experience in scripting, tooling, automation, and Infrastructure as Code (IaC) frameworks
  • In-depth knowledge and experience of monitoring frameworks such as Zabbix/GreyLog
  • Excellent understanding of traditional ops areas of expertise: Windows/Linux, Networking etc.
  • Good familiarity with docker and container ecosystem including technologies such as Kubernetes
  • Quick to spot opportunities and new capabilities in technologies
  • Familiar with database technologies such as MySQL and MSSQL
  • Comfortable in complex provisioning and deployment scenarios, modern CI/CD pipelines
  • A strong collaborator, organised, and has a safe pair of hands
  • A team player that enjoys influencing change, leading and developing a technical function
  • Comfortable communicating to mixed audiences of Support, Product Delivery, Engineering, and Incident Management
  • Critical thinking skills, a delivery-oriented attitude, and attention to detail.
  • Minimum 5 years’ experience building, deploying and maintaining production software.


What we value

Passion, Teamwork, Innovation and Professionalism are the values we believe make us the company we are. We are looking for someone who understands great culture and will help us shape it as it evolves.

Powered by JazzHR

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Executive Director, Feasibility, Site and Patient Engagement

Precision Medicine Group

Edinburgh, Scotland
30+ days ago
Edinburgh, Scotland
30+ days ago
Position Summary:
The Executive Director, Feasibility, Site and Patient Engagement has responsibility for the oversight of the delivery of pre award feasibility, the process for the post award feasibility, the management of the Precision Site Network, site engagement approach initiatives and the collaboration and involvement of patient advocacy groups. This individual will be part of the management level of the Operational Strategy department. They will play an important role in setting and achieving department goals, and as part of the Operational Strategy Department, will contribute and support colleagues in the achievement of company goals.
 
Essential functions of the job include but are not limited to:
• Oversees the Precision Clinical Solutions Feasibility, Site and Patient Engagement functional area.
• Line manages Feasibility, Site and Patient Engagement dedicated staff.
• Establishes the aims, processes and implementation of Feasibility, Site and Patient Engagement in support of Precision study pre-award activities.
• Establishes process and training to support post study award Feasibility, Site and Patient Engagement.
• Expands and oversees the Precision For Medicine Site Network (PSN) globally:
• Establishes the business mission of the PSN in alignment with the strategic company goals and Senior Management
• Establishes and oversees the aims,  methods and processes for the Precision Site Network including: network site selection and performance criteria, conduct and maintenance of site assessment, management of metrics, role of the PSN pre study award and post study award
• Expands the PSN globally and across Precision target specialist areas, including individual site networks in Oncology, Rare/Orphan Disease, Cell/Gene Therapy, Neurology/CNS, Autoimmune/Allergy, Paediatric and Companion Diagnostics
• Acts as an escalation point within the Operational Strategy Department for queries and escalations from the Precision Site Network. Contributes to the development of excellent and dependable site relationships.
• Liaises with project management, operational strategy and business operational leads to continually refine process in order to meet evolving client and study needs.
• Oversees the methods to enhance and expand site relationships that are outside of the network to provide more continuity for sponsors and project teams.
• Engages and collaborates, where applicable and possible, with targeted advocacy groups to further the mission of the overall network
• Where required, act as an escalation point for PSN issues raised for pre and post award studies
• Oversees the building and management of feasibility functional area.
• Establishes process, templates and delivery standards for feasibility pre and post award
• Works with Business Operations and Operational Strategy colleagues to select platforms, IT solutions, strategic partnerships and vendors to enhance the quality of feasibility, to enhance pre-award data and post study award enrolment planning and achievement
• Manages the delivery of data driven and site outreach feasibility for pre award opportunities
• Manages the supports and training provided to project management for data driven and site outreach feasibility for awarded studies
• Attends conferences as appropriate to support the establishing and growth of the Feasibility, Site and Patient Engagement
• Establishes and maintains process to structure a feasibility, site and patient engagement expertise and information center that can be consulted for pre and post study award.
• Establishes process and oversees engagement with patient advocacy groups in order to support study feasibility, recruitment and successful delivery
• Collaborates with Operational Strategy and Business Operations to implement a robust Investigator/PI Database
• Provides active participation and leadership support to corporate initiatives involving site and patient engagement
• Collaborates with the corporate training department to provide pre and post award site training strategy and material input
• Provides company budget input and management for the financial requirements of the Feasibility, Site and Patient Engagement.
• Support Business Development in client meetings and bid defense presentations.

Qualifications:
Minimum Required:
• 4-year college degree or equivalent experience ideally in a scientific or healthcare discipline.
• A minimum of 15 years in the CRO/pharmaceutical industry supporting clinical trials and overall drug development

Other Required:
• Proven experience in global clinical operations and project management, with specific expertise in Phase I-IV Drug Development
• Demonstrates strong and successful leadership and accomplished in leading cross-functional teams in Phase I-IV drug development
• Possesses strong budget management experience
• Direct supervisory experience
• Excellent organizational and communication skills with computer proficiency (at a minimum Excel, MS PPT)
• Professional use of the English language; both written and oral
• Domestic and international travel including overnight stays
 
 
Competencies:
• Accomplished in global project leadership with a balanced strategic focus, creativity, sound judgment and decision making skills
• Accomplished at maintaining a sustained focus at the macro level while being able to manage at the micro level as needed
• Collaborates with project teams in setting objectives, tracking progress and resolving complex project challenges
• Focuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient and people more effective in delivering results with appropriate quality and timeline performance
• Leads, inspires and ensures appropriate ownership and accountability of project leaders in a highly virtual and matrix-managed organization
• Accomplished in building and maintaining positive client relationships
• Proven ability to effectively influence, negotiate and manage conflict
• Demonstrates awareness and understanding of strategic goals/priorities and focuses on the most important organizational priorities
• Proven financial management skills
• Exhibits high self-motivation and is able to work and plan independently as well as in a team environment
• Effective mentor and coach with proven ability to identify individual development needs
• Proven ability to effectively listen, collaborate and proactively seek solutions orientated outcomes
• Embraces and embodies the established Precision for Medicine’s Cultural Values as an underlying tenet to drive work behaviors
• Accomplished at maintaining excellent communication lines to ensure relevant information effectively flows up and down the organization
• Demonstrates mastery knowledge of ICH-GCP, relevant Precision for Medicine’s SOPs and regulatory guidance, as well as the ability to implement such items.
• Demonstrates insight and creativity and readily offers solutions to facilitate resolution
• Strong writing skills
• Strong presentation skills
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Clinical Trial Associates or Senior Clinical Trial Associates - CRO - Oncology REMOTE

Precision Medicine Group

Edinburgh, Scotland
30+ days ago
Edinburgh, Scotland
30+ days ago

Precision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

We offer opportunities for both CTAs and Senior CTAs who will be providing administrative support to project teams in clinical operations. You will support several clinical programs and participate on a number of project teams as a valued member of the Project Team contributing towards efficient management of trials. Senior level CTAs serve as Subject Matter Experts with a focus on mentoring and training.

About You:

  • You are calm, thoughtful, and responsive when things don’t go as planned.
  • You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
  • You find quick and creative ways of overcoming difficulties.
  • You have an impeccable eye for detail.
  • You identify potential study risks and know how to mitigate them.
  • You are adept at handling conflict by using tried and true resolution strategies.
  • You are ambitious, collaborative, agile, and a standout colleague.

How we will keep you busy and support your growth:

  • Handling inventory, tracking, and shipping for clinical trials supplies (consisting of CRFs, study drug where applicable, and other supplies)
  • Assisting with preparation and shipment of Operating Manuals
  • Developing and maintaining the study specific investigator database for use with correspondence and mail merges
  • Updating and maintaining study tracking including a master team contact list
  • Preparing and distributing initial site start up packages and liaises with the sites to obtain required regulatory documents
  • Assisting team leaders in the production of study reports and updates
  • Serving as an office based point of contact for all sites during the course of the study as well as provides phone coverage for travelling team members
  • Preparing investigator budget payments and distributing to sites
  • Serving as administrator of the Trial Master File with direction from Project Management, including the preparation, maintenance, and archiving of the TMF
  • Identifying and processing Serious Adverse Events according to the procedures defined by the study team
  • Assisting with study start-up of clinical trials, including feasibility, investigator recruitment, collection of regulatory documents and general site management support

Qualifications:

Minimum Required:

  • UK GCSE or equivalent local level qualifications

Other Required:

  • Experience in a Clinical Trial Administration role or related discipline; CTAs will have 1-3 years and Sr. CTAs will have 3-5 years of experience
  • Basic computer skills, including word processing
  • Working knowledge of ICH-GCP, SOPs, and regulatory guidance including a good knowledge of the regulatory and safety processes
  • Limited travel may be required for this position

Preferred:

  • CRO experience

About Precision for Medicine

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping our clients harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.

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Posted

1 day ago

Description

Health & Safety Manger








Req ID: 97480








Location:

Tranent, GB, EH33 2NE














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, we’ll help you build a career that you can feel passionate about.




Job Summary



At our world class facility in Elphinstone, Tranent (close to Edinburgh), our Health & Safety Department currently has an exciting career opportunity for aHealth & Safety Manger.





Department Information





The Health and Safety department encompasses a wide variety of health and safety activities including, updating procedures, training, incident management, auditing and risk assessment. The main hazards on site are associated with COSHH (chemical and biological), manual handling, ergonomics/work station assessment and the use of radio-chemicals. There are also some unique operational process hazards as well as the more standard workplace safety considerations. The Health and Safety department currently provides support across four sites although the role will be based within the Elphinstone Research Centre site.





Key Responsibilities:






+ Management of the health and safety department


+ Management of incident reporting process


+ Advise and support departmental health and safety audits


+ Advise and support departmental COSHH assessments


+ Advise and support departmental risk assessments


+ Carry out health and safety training


+ Manage health and safety contractors


+ Chair management health and safety meetings and projects


+ Produce and communicate safety KPIs to senior site management


+ Provision of support, advice and monitoring of matters relating to Health and Safety to all levels of staff


+ Responsible for radiochemical use reporting and regulatory compliance requirements to SEPA


+ Liaise with and report to HSE as appropriate






Applicants should have:






+ A minimum of NEBOSH Certificate


+ Excellent influencing skills and enthusiasm for creating/maintaining a positive health and safety culture by application of continuous improvement


+ Proven experience of


+ Risk Assessments


+ Incident reporting/ investigation


+ Safety auditing


+ COSHH




+ A good understanding of health and safety legislation and its application within the workplace together with some practical work experience, ideally gained in a scientific, healthcare or engineering context.


+ Computer literacy is essential (competency of MS Office) and you must be capable of working on your own initiative.


+ You must be flexible, detail conscious and well organised






Salary for this position with be dependant on the candidates skills and experience.





The closing date for this vacancy is Friday, 12 March 2021.








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 17,000 employees within 90 facilities in 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. And in 2019, revenue increased to $2.62 billion.





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 supported the development of ~85% of the drugs approved by the FDA in 2019.











Source: Charles River Laboratories