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Job Details

Consultant for Non Clinical Safety Issues

Company: Regulatory Professionals
Location: UK Wide
Reference: J32403
Closing Date: 05 Mar 18
Type: Contract
Salary (£): Negotiable
Benefits: Competitive

Job Summary:

Consultant for Non Clinical Safety Issues This internationally recognised pharmaceutical firm seeks an experienced regulatory affairs consultant to assist with non clinical safety issues on an ad hoc basis.

Requirements:

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

Apply for this job: Consultant for Non Clinical Safety Issues

Contact Information:

Address:  UK Office
3rd floor 33 Blagrave Street Reading
RG1 1LG
England
Tel:  +44 (0)118 9522 797
Website:  Visit Our Web Site

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