Pharmacovigilance is one of the most closely regulated areas of the industry, and it never switches off. Safety teams monitor, assess and report on the risks of medicines throughout their lifecycle, and the people doing that work need to be accurate, thorough and confident under scrutiny.
We help pharmaceutical, biotech, CRO and medtech organisations build PV and drug safety teams that stay compliant and keep patients at the centre. We recruit from entry level through to Director and above, in the UK and internationally.
Roles we recruit include:
- Drug Safety Associates and Case Processors
- Safety Scientists and PV Scientists
- Safety Physicians and Medical Reviewers
- Signal Detection and Risk Management Specialists
- Aggregate Reporting Specialists (PSURs, PBRERs, DSURs)
- Qualified Persons for Pharmacovigilance (QPPVs)
- PV Quality, Compliance and Audit Specialists
- Heads of Pharmacovigilance and Drug Safety
What we look for in every PV candidate
- Regulatory fluency: working knowledge of GVP, MHRA and EMA requirements, and FDA expectations where relevant
- Attention to detail: accuracy in case assessment and reporting, where small errors carry big consequences
- Systems experience: hands-on use of safety databases such as Argus or ArisG, matched to your platform
- Sound judgement: the confidence to make clear, defensible decisions on safety data
- Inspection readiness: experience of audits and inspections, and the discipline to keep documentation in order
Flexible support for a demanding function
Safety workloads can change quickly with a new product launch, a merger or a surge in case volumes. We support permanent, contract and interim hiring, so you can scale your team without compromising on quality or compliance.
