Regulatory Professionals

Consultant for Non Clinical Safety Issues

Location
UK Wide
Salary
Negotiable
Posted
20 Aug 2019
Closes
28 Aug 2019
Ref
J32403
Discipline
Quality, QA / QC
Contract Type
Contract
Consultant for Non Clinical Safety Issues

Ad hoc contract basis

Location; Remote

This internationally recognised pharmaceutical firm seeks an experienced regulatory affairs consultant to assist with non clinical safety issues on an ad hoc basis. Offering 100% remote support you will liaise via skype, phone or email. Support provided will include study data for toxicology studies, data presentation in regulatory documents, impurities, leachables and extractables, pre clinical development plans, NDA"e;s and Scientific Advices.

Candidates requirements include;

- The ideal candidate with have a toxicology background or comparable postgraduate specialisation
- Knowledge of preclinical drug development is advantageous
- 5 years regulatory experience within a pharmaceutical environment

Job Reference; J32403

consultancy, regulatory affairs, non clinical, safety issues, toxicology studies, pharmaceutical industry, regulatory documents, preclinical, pre clinical drug development, drug development, home based, remote

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