jobid=A.0.0501
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Apsida Life Science has partnered with a leading research organization to present the following role:
Job Title
Regulatory Affairs Consultant
Location
Remote, Netherlands
Company Overview
The client company is a leading research organization conducting clinical trials on behalf of pharmaceutical and biotechnology clients to expedite drug development and clinical trial progress. It is one of the largest research organizations in the world, providing a full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster.
Responsibilities
- Perform Product registration and Approval procedures via EU centralized procedures.
- Familiar with Blue Box requirements, including pictograms and specific symbols.
- Perform and be familiar with pre-submission regulatory requirements.
- Understand post-submission obligations.
- Perform mockups prior to launch or during submission.
Qualifications
- Relevant Degree in Pharmacy, Chemistry, or any relevant Life Science Degree.
- Regulatory Affairs Training certifications and/or qualifications.
- Registered Freelancer is a plus.
If you are interested in learning more, please reach out to Mufaro Mpofu.
Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA), and Pretoria (South Africa). We are dedicated to delivering the best talent to the Life Science industry. We believe there is a market gap for a cost-effective, high-quality, and trusted recruitment service that prioritizes the candidate journey.
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