Providing solutions and products for patients is the core aim for life sciences companies and it is the pharmacovigilance and drug safety teams that ensure risks and side effects are kept to a minimum.
Crucial to the success of any drug launch or product development, PVG and drug safety professionals aid with the assessment, reporting and protection of patient safety throughout the process.
- Global Drug Safety
- Post market Drug Safety
- Clinical Drug Safety
- Case Processing
- Drug Safety Systems
- Drug Safety Audits
Our dedicated pharmacovigilance team builds long-term relationships with exceptional candidates and has a wide network of high-quality candidates within the pharmacovigilance, drug safety and clinical safety industry, many of who choose to work with us exclusively and can't be easily accessed by other recruiters.
Working across the global pharmaceutical, biotech, medical device and CRO sectors, our specialist consultants source solely for pharmacovigilance and drug safety roles which may have a UK affiliate, European or global focus. As industry experts, they all have an in-depth level of knowledge in their field, which they use to help our clients navigate developments within the drug safety industry.
For example, Brexit is impacting EU QPPR positions as these professionals will need to be based within the EU in order to operate compliantly. Hobson Prior’s drug safety specialist recruiters are helping support companies impacted by this transition by supporting with international candidate relocation and sourcing local QPPRs within the UK to minimise the impact of Brexit