Pharmacovigilance & Regulatory
Our experienced pharmacovigilance team help to assure the quality and integrity of data submitted to the FDA or other regulatory authorities by reviewing your submitted content. At Guires, we perform a critical review of the following:-
- Identifying the adverse effects of pharmaceutical drugs
- Assessing the risks and benefits of medicines
- Determining ways to improve the safety of certain drugs
- Providing information to users on using medicines safely and correctly
- Monitoring the effects of any changes made on pharmaceuticals
We recruit for various job roles in a broad range of pharmaceutical specialist disciplines. Some of these sector disciplines include:
- Pharmacovigilance officer and assistant jobs for database entry, tracking and compliance
- Drug safety scientist
- Coordinators and case-processing specialist pharmacovigilance
- Senior pharmacovigilance associate for handling Periodic Safety Update Reports (PSURs)
- Senior manager and director of pharmacovigilance for the strategic planning of pharmacovigilance departments, implementation of new systems and line management
- Regulatory Project Manager
- Regulatory Operations Associate
- Regulatory Submissions Associate
- Regulatory Consultant
- Regulatory Affairs Director
- Regulatory Manager in Submissions Compliance
- Regulatory Manager in Intelligence and Compliance
- Regulatory Affairs Document Management Officer
- Regulatory Affairs Executive
- Regulatory Affairs Administrator
- Regulatory Affairs Manager
- Head of Regulatory Affairs
- Health Economist
- Outcomes Research Manager / Associate
- Market Access Manager / Associate / Director
- Health Outcomes Manager / Associate / Director
- Reimbursement Manager / Associate / Director
- Director of Health Economics
- Modeller / Senior Modeller
- Permanent Contingency recruitment
- Contract Recruitment
- In Sourced Contractors
- Interim Assignments
- Executive Search and Selection
- Advertised Selection
