CK Group are recruiting for a Regulatory Associate to join a company in the healthcare industry at their R&D site based in Ware initially on a contract basis for 12 months.
£25.56 per hour Umbrella
Regulatory Associate Role:
To assist in the preparation of the nonclinical content for various global regulatory dossiers
? Data mining existing and historic dossiers and company archives to identify and locate nonclinical studies
? Compilation of complete and accurate nonclinical study reports package for onward submission
? Tracking progress of activities and effectively communicating with team and stakeholders to progress collation/preparation and hand over of nonclinical data and documentation
? Collaboration with EEU Rebaseline Team and managing literature references
? Minimum graduate level, with a relevant biologically based scientific background
? Understanding of the nonclinical content related to in vivo and in vitro testing: ie pharmacology, pharmacokinetics & toxicology related to drug development
? Excellent written and verbal communication skills, computer literate and competent in the use of Microsoft Word and Excel
? Proficiency in searching on-line scientific publication databases
Knowledge of nonclinical regulatory requirements [e.g., Common Technical Document (CTD) guidelines] would be preferable but not essential.
Our client is a global healthcare company, taking on some of the world\'s biggest healthcare challenges.
This Regulatory Associate role will be based at our clients R&D site in Ware, Hertfordshire.
Entitlement to work in the UK is essential. Please quote reference 51543.
Please note that the successful applicant will be required to engage via an FCSA-accredited and CK-approved umbrella company and the rate of pay indicated is an umbrella rate.
You must be eligible to work in the UK. Learn more
- Agency: CK Group
- Contact: Heather Deagle
- Phone: 0191 384 8905
- Reference: 51543
Website: CK Group
- Updated: 20th September 2021
- Expires: 18th October 2021