Report Coordinator - Harrogate, UK

Spacey Houses
13 Nov 2017
16 Nov 2017
Contract Type
Full Time
COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.

We are recruiting for our Early Compound Development Unit in Harrogate and are currently seeking to hire a Report Coordinator to support the Report Coordination team. This is a full time permanent position, based at our site in Harrogate.

About the Job

The Report Coordinator will manage a full study workload with complex study designs by adhering to report preparation schedules and prioritizing tasks. They will identify and resolve changes to established study schedules and ensure client deliverables are met.

The Report Coordinator learns and performs the duties of drafting and finalizing nonclinical study reports and completes the following duties with limited supervision:

- Prepare the study report using details described in the protocol, protocol amendments, and study communications and Covance or client-specific requirements.
- Addresses any quality assurance inspection items on GLP-regulated studies.
- Finalizes study reports and obtain, prepare, and deliver materials to archives.
- Prepare data tables including completing basic statistical analysis in table generation programs and reviews data tables for accuracy.
- Draft and quality check data tables that were manually prepared.
- Review and adjust the reporting schedule to ensure client expectations are met.

We Offer

The opportunity to work within an experienced and highly skilled team.

Covance offers a comprehensive benefits package including health cover and contributory pension. Covance's ongoing success offers team members unsurpassed growth and career development opportunities. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. This is your chance to become part of a team that helps to bring miracle of medicine to market sooner. There is no better time to join us!

Education / Qualifications

To be successful in this position, you will need to hold a Bachelor's degree or equivalent experience. Degree and/or experience in technical writing, document production/publishing, and/or science preferred.

Additionally, you will need to demonstrate:

- Knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®).
- Attention to detail, time management skills, and organizational skills.


Ideally at least 1 year of technical writing or data tabulation experience, especially in pharmaceutical research or life sciences.