Administrative Assistant Location: Geneva, Switzerland Sector: Pharma Start: 12/2021 Duration: 12MM+ Ref.Nr.: BH17786 Your tasks: * Being responsible for calendar management * Planning meetings and calls * Coordinating travels including the booking and more * Working on expenses man...

The Senior Safety Scientist supports early and late phase development activities as a member of the safety team under the leadership of the Safety Science Leader (SSL) providing essential safety oversight and input into all aspects of study management across the entire development portfolio. In...

The Senior Safety Scientist supports early and late phase development activities as a member of the safety team under the leadership of the Safety Science Leader (SSL) providing essential safety oversight and input into all aspects of study management across the entire development portfolio. In...

The Pharmacovigilance Scientist will be responsible for the timely case management of spontaneous and clinical trial reports including the data entry, QC, follow-up, E2b electronic reporting of adverse reactions received from worldwide sources; in addition, reporting of events to Ethics Committ...

I am currently recruiting for a PV Physician to join a client on a permanent basis. Within this role you will execute and manage Pharmacovigilance projects global clients. This role is 100% home based! Responsibilities: *Author Risk Management Plans (RMP) and review of RMP updates *Medical R...

My pharmaceutical client in the Berkshire area is looking for a PV Scientist on a part time contract basis for 9-12 months. The Pharmacovigilance Scientist will be responsible for the case management of spontaneous and clinical trial reports such as the data entry, QC, follow-up, E2b electroni...

I am currently recruiting for an interim PV Physician to join a client on an initial 3 month contract basis. Within this role you will execute and manage Pharmacovigilance projects global clients. This role is 100% home based! Responsibilities: *Author Risk Management Plans (RMP) and review ...

The Pharmacovigilance Scientist will be responsible for the timely case management of spontaneous and clinical trial reports including the data entry, QC, follow-up, E2b electronic reporting of adverse reactions received from worldwide sources; in addition, reporting of events to Ethics Committ...

Within this role you will provide principal subject matter expertise for the design, development, maintenance & support of core PDS processes. This is a key enabling and strategic role, ensuring that the client can continue to deliver effective scientific safety activities and/or PV system acti...

An excellent opportunity has arisen for a Pharmacovigilance Manager to join an expanding team based in West London. The ideal candidate will have a strong background in processing and reviewing individual case safety reports, author and review aggregate reports and maintenance of drug dictiona...

An excellent opportunity has arisen for a Pharmacovigilance Manager to join an expanding team based in West London. The ideal candidate will have a strong background in processing and reviewing individual case safety reports, author and review aggregate reports and maintenance of drug dictiona...

An excellent opportunity has arisen for a Pharmacovigilance Manager to join an expanding team based in West London. The ideal candidate will have a strong background in processing and reviewing individual case safety reports, author and review aggregate reports and maintenance of drug dictiona...

An excellent opportunity has arisen for a Pharmacovigilance Manager to join an expanding team based in West London. The ideal candidate will have a strong background in processing and reviewing individual case safety reports, author and review aggregate reports and maintenance of drug dictiona...

An excellent opportunity has arisen for a Pharmacovigilance Manager to join an expanding team based in West London. The ideal candidate will have a strong background in processing and reviewing individual case safety reports, author and review aggregate reports and maintenance of drug dictiona...

An excellent opportunity has arisen for an experienced PV Manager to join a relentless and passionate team based in Hertfordshire. Within this role you will manage the UK PV Operations team. Responsibilities: *Continue to work effectively, efficiently and build even stronger relationships w...

An excellent opportunity has arisen for an experienced PV Manager to join a relentless and passionate team based in Hertfordshire. Within this role you will manage the UK PV Operations team. Responsibilities: *Continue to work effectively, efficiently and build even stronger relationships w...

An excellent opportunity has become available for an experienced PV Writer to join my client on a home based contract basis. Within this role you will be responsible for authoring Pharmacovigilance aggregate reports, including PBRERs, DSURs and RMPs. Evaluation of aggregate safety data and ...

An excellent opportunity has arisen for an experienced PV Manager to join a relentless and passionate team based in Hertfordshire. Within this role you will manage the UK PV Operations team. Responsibilities: *Continue to work effectively, efficiently and build even stronger relationships w...

An excellent opportunity has arisen for an experienced PV Manager to join a relentless and passionate team based in Hertfordshire. Within this role you will manage the UK PV Operations team. Responsibilities: *Continue to work effectively, efficiently and build even stronger relationships w...

An excellent opportunity has arisen for an experienced PV Manager to join a relentless and passionate team based in Hertfordshire. Within this role you will manage the UK PV Operations team. Responsibilities: *Continue to work effectively, efficiently and build even stronger relationships w...

An excellent opportunity has arisen for an experienced PV Manager to join a relentless and passionate team based in Hertfordshire. Within this role you will manage the UK PV Operations team. Responsibilities: *Continue to work effectively, efficiently and build even stronger relationships w...

An excellent opportunity has arisen for an experienced PV Manager to join a relentless and passionate team based in Hertfordshire. Within this role you will manage the UK PV Operations team. Responsibilities: *Continue to work effectively, efficiently and build even stronger relationships w...

The Case Management Specialist, Submissions & Reconciliation is responsible for the timely reconciliation and submission of Individual Case Safety Reports (ICSRs) to and from destinations including but not limited to global regulatory authorities, business partners, investigators, and ethics co...

My client, a Top 10 Pharma client based in Buckinghamshire, currently seeks an experienced PV Manager to join their team on an initial 12 month contract basis. Within this role you will be responsible for the management of local PV staff. Safety Management and Reporting * Act on behalf of t...

An excellent opportunity has arisen for an experienced PV Manager to join a relentless and passionate team based in Hertfordshire. Within this role you will manage the UK PV Operations team. Responsibilities: *Continue to work effectively, efficiently and build even stronger relationships w...