Pharmacovigilance PV Operations Manager
- Employer
- Sensible Staffing
- Location
- UK
- Salary
- Competitive
- Closing date
- 1 Jun 2022
View more
- Sector
- Healthcare
- Contract Type
- Permanent
- Hours
- Full Time
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I am currently recruiting for a Pharmacovigilance Operations Manager to work at a Pharmaceutical homecare based in Burton-upon-Trent.
You will be responsible and accountable for the day-to-day management of pharmacovigilance operations including but not limited to; end to end case handling, reconciliation, operation of the safety database, case reporting and quality control.
The PV operations manager plays a key role in the PV function facilitating across functional teams, building relationships, supporting the delivery of PV Agreements to ensure timely and accurate collection, processing and reporting of safety information data in compliance with contractual and regulatory obligations.
You will ensure all operational tasks required for clients are completed to regulatory requirements, balancing quality, efficiency, and cost whilst ensuring oversight and correct documentation is in place.
Suitable candidates should have experience in a regulatory background, exposure of patient safety, continuous improvement, liaising with pharma companies in regards to audits.
This is a full time role working in a hybrid pattern. Intially you will be required to attend the site in Burton 5 days per week whilst being trained up. This will then reduce to 1 day per week, with the rest working from home.
If you are interested, please apply or email your CV directly to
You will be responsible and accountable for the day-to-day management of pharmacovigilance operations including but not limited to; end to end case handling, reconciliation, operation of the safety database, case reporting and quality control.
The PV operations manager plays a key role in the PV function facilitating across functional teams, building relationships, supporting the delivery of PV Agreements to ensure timely and accurate collection, processing and reporting of safety information data in compliance with contractual and regulatory obligations.
You will ensure all operational tasks required for clients are completed to regulatory requirements, balancing quality, efficiency, and cost whilst ensuring oversight and correct documentation is in place.
Suitable candidates should have experience in a regulatory background, exposure of patient safety, continuous improvement, liaising with pharma companies in regards to audits.
This is a full time role working in a hybrid pattern. Intially you will be required to attend the site in Burton 5 days per week whilst being trained up. This will then reduce to 1 day per week, with the rest working from home.
If you are interested, please apply or email your CV directly to
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