- Excellent opportunity to join a global leading pharmaceutical business
- Great opportunity to be apart of a dynamic team working on exciting projects
About Our Client
My client is a global leading Pharmaceuticals business
Provide preclinical expertise to support to the development of nonclinical overviews and summaries (e.g. nonclinical CTD modules 2.4, 2.6.x) to support registration renewals and new license applications
The Successful Applicant
Minimum 5-10 years experience providing preclinical scientific contributions to regulatory submission documents, specifically nonclinical pharmacology content of ICH-compliant CTD modules 2.4 and 2.6.1-2.6.5.
Significant experience (5-10 years+) in the Pharmaceutical or Consumer Healthcare industry.
What's on Offer
Excellent day rate opportunity
Contract duration - circa 10 months