Assistant Report Publisher 1
Tranent, GB, EH33 2NE
For 75 years, Charles River employees have worked to advance the discovery, development, and safe manufacture of new drug therapies, making a profound impact on global health. Our 20-year partnership with Boston Children’s Hospital takes this mission to the next level, supporting groundbreaking innovations that directly impact patient care. At Boston Children’s, their commitment to diversity drives the exceptional quality of care provided to patients from local communities to over 160 countries worldwide. This is your moment to become part of a family where unique talents and perspectives unite to change lives, including your own. Together, we’re shaping a healthier future through compassion, innovation, and opportunity.
Job Overview
We have an exciting career opportunity for an Assistant Report Publisher. This role is full time, on site (with hybrid options after a period of training), and is located in our world class facility in Tranent (EH33 2NE).
Due to our continued growth and success, we can offer rewarding opportunities in a research environment. The Assistant Report Publisher will compile scientific reports and documents to meet Sponsor and regulatory standards and ensure issue of reports in line with protocol deadlines.
This role is perfect for someone who takes pride in creating clear, polished, and well organised documents that truly make an impact. You’ll be at the heart of bringing information together, carefully formatting and structuring content, building intuitive tables of contents, and working closely with client documents, often within tight deadlines.
This role is offered Full time, (Hybrid working is available after an initial training period) the Salary of £25,352.56 per annum as well as 29 days paid Holidays, Pension, Private Healthcare, Health Insurance, Employee discount scheme, Free Gym on site, Cafeteria with great food, Free onsite parking and more.
Key Responsibilities and Experience
Key Responsibilities
- Compile and publish reports using Charles River and client’s own templates to conform to Sponsor and regulatory requirements using Adlib publishing system, MS Word, Adobe Acrobat and associated publishing tools.
- Work collaboratively with Study Directors on their scientific reports.
- Format check and pdf phase reports from internal contributing areas to ensure regulatory compliance.
- Ensure that all reports are of a high standard by checking of own work before the QC process.
- Handle special customer requests, such as expedited timelines and custom formats.
- Ship reports to clients to meet deadlines.
- Serve as a subject matter expert on reporting standard and Sponsor requirements.
Experience and requirements
- Proven excellent skills in Microsoft Word and Adobe – able to format, apply and modify styles, tables of contents and hyperlinks.
- Detail oriented with a good eye for how text and graphics look.
- Ability to work within a pressured environment and to tight deadlines.
- Good, confident communication and people skills which enable you to effectively collaborate with internal/external employees of all levels.
- Ability to work independently.
About Insourcing Solutions
Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space.
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 over 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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
Equal Employment Opportunity
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
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