Skip to main content

This job has expired

Biologics Project Coordinator

Employer
Charles River Laboratories - Scotland
Location
Tranent, United Kingdom
Salary
Competitive
Start date
9 Mar 2023
Closing date
23 Mar 2023

View more

Discipline
R & D , Biology
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

For 75years, 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.

IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.

Job Summary

Does being in the heart of a business interest you?

Are you interested in the maintaining of accurate financial and scientific data?

Then this could be the role for you!

Charles River are recruiting a talented, highly motivated Project Coordinator in the Biologics European Project Coordination team, to have responsibility for ensuring accurate reporting of the financial revenue forecasting and recognition of scientific projects in the Biologics Business. This role can be based at our Edinburgh site or remote, and you will be working closely with Scientific Operations in Germany, Ireland and England as well as our colleagues in the US.

You will receive comprehensive training in all aspects of the role, and we're looking for enthusiastic, driven applicants who are eager to learn and establish their career with a global organisation.

What You'll Be Doing

• Working with our Enterprise Resource Planning System, SAP.
• Reviewing contracts and acceptable documentation to build financial costs and study designs in SAP.
• Ensuring sales orders and study schedule are created & updated accurately, and releasing invoicing milestones.
• Contribute to process improvement and integration as we grow as an internal Charles River Business.

Skills and Qualifications
• Applicants should preferably be educated to degree level or have other relevant qualifications / experience.
• Well organised and confident with an eye for detail and the ability to complete jobs under pressure.
• Proactive approach to working and the ability to plan work ahead of time and prioritise work depending on business schedules.
• Effective verbal and written communication with internal colleagues.
• Excellent numeracy and literacy skills.
• A dynamic and flexible approach towards achieving departmental objectives.
• Enthusiasm to contribute to ideas for continuous improvement.
• Experience in Microsoft Excel is essential but any knowledge or awareness gained from working in a scientific department with a variety of study designs and an understanding of Good Laboratory Practice and/or knowledge or experience with SAP would be an advantage.
• Models the Charles River Values of Care, Lead, Own and Collaborate.

What We Offer You
• A very comprehensive benefits package from day one, including a large pension contribution, private medical, and more!
• The opportunity to get industry standard training and experience.
• Global opportunities and strong career progression.
• Personal development and skills enrichment as one of our key focuses.
• To be able make a difference to health and well being of people.
• Flexible working opportunities.

Salary depending on experience.

The closing date is 22 March 2023.

Profile and Requirements

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

For more information, please visit www.criver.com.

Company

Find out more about working for our company

crl career hub button

Brief Company Description;

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.

  Here in Scotland, based at our site in Tranent, East Lothian, we offer a complete array of Safety Assessment services from complete IND-enabling programs to stand-alone preclinical studies, our preclinical CRO services provide a full range of in vivo and in vitro testing evaluations and regulatory support for the safety assessment of pharmaceuticals, medical devices, and animal health products as well as chemicalsagrochemicals, and biocides. Our scientific and regulatory staff develop and execute individual preclinical studies or customized programs to ensure that drug efficacy and safety assessments are conducted in the most efficient manner.

 

Company info
Website
Mini-site
Charles River Laboratories - Scotland
Location
Elphinstone Research Centre
Tranent Easy
Lothian
EH33 2NE
United Kingdom

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert