Assistant Report Publisher 1

3 weeks ago


Tranent, United Kingdom Charles River Laboratories Full time

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 Report Centre currently has an exciting career opportunity for an Assistant Report Publisher.

Due to our continued growth and success, we can offer rewarding opportunities in a research environment. The Assistant Report Publisher will produce scientific reports to meet Sponsor and regulatory standards and ensure issue of reports in line with protocol deadlines.

Key Responsibilities:

- To compile and publish reports using Charles River and Sponsors’ own templates to conform to Sponsor and regulatory requirements using Adlib publishing system, MS Word, Adobe Acrobat and associated publishing tools
- To format check and pdf phase reports from internal contributing areas according to ensure regulatory compliance.
- Ensure that all reports are of a high standard by checking of own work before the QC process.
- Ship reports to clients to meet deadlines

Applicants should have:

- 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
- Minimum 5 standard grades (or equivalent) including English or experience working in a similar role

The salary for this position is £22,563.88 per annum.

The closing date is 16 January 2023.

**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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