Regulatory Specialist/Manager (Toxicology)

Regulatory Specialist/Manager (Toxicology)

PPD - Pharmaceutical Product Development

Brussels, Belgium

In this role you will be a pivotal team member with a solid experience in the field of drug development and awareness of regulatory requirements to enable clinical trials. You may be involved in advising on nonclinical safety evaluation strategy across projects, design toxicity studies according to current regulatory guidelines, coordinate internal and external review of study plans, study results, and study reports, support writing of regulatory documents (e.g. IND, IMPD, Investigator’s Brochure).

Qualifications

Education and Experience Requirements:

  • Ideally candidates will have an Advanced scientific degree (Master or PhD degree);
  • Experience in the field of drug development;
  • Experience in nonclinical safety testing of biologics and antibodies;
  • Spoken and written English and French.

The soft skills include but not limited to:

  • Excellent organizational and communication skills;
  • Show proven scientific communication skills with regards to scientific report writing and informal and formal oral presentations (English);
  • Strong collaborative and interpersonal skills;
  • Problem solving skills;
  • Flexibility and Adaptability.

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© EuroJobsites 2020

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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