Pharmacovigilance Specialist - Life Science - Contract - Remote, UK
Our client is a global leading life science organisation. At present they are seeking a Pharmacovigilance Specialist on a 12 month contract basis. The role will be predominantly remote based with some travel to their site in West London (once or twice per month).
The role:
You will be a core member of the Global Safety & Pharmacovigilance team. The purpose of the role is to support the International Pharmacovigilance (IPV) team and Safety Officer network in routine regional and operational activities. The role also supports the development and implementation of strategy and projects to optimize the cohesiveness of the IPV function and Safety Officer network in all PV activities. The IPV Specialist also facilitates communication and coordination between IPV and Safety Officers.
Support IPV function with two-way communication with the Safety Officer network and GSPV functions, ensuring timely responses to queries, organization of meetings, production of written communication, etc. Coordinate routine tasks such as onboarding and offboarding activities for Safety Officers, PSMF updates, reconciliation, etc. Maintain the appropriate documentation necessary for IPV activities, such as Safety Officer contact details, nomination documents, procedural documents if applicable, etc. Participate and contribute to projects aimed at developing and implementing local and global PV processes which are both compliant with legislation and integrated into CSL's PV system. Support directly IPV Heads and Territory Managers with all other IPV-related activities as necessary.
This project will be looking to commence from January 2025 for 12 months. #J-18808-Ljbffr
Our client is a global leading life science organisation. At present they are seeking a Pharmacovigilance Specialist on a 12 month contract basis. The role will be predominantly remote based with some travel to their site in West London (once or twice per month).
The role:
You will be a core member of the Global Safety & Pharmacovigilance team. The purpose of the role is to support the International Pharmacovigilance (IPV) team and Safety Officer network in routine regional and operational activities. The role also supports the development and implementation of strategy and projects to optimize the cohesiveness of the IPV function and Safety Officer network in all PV activities. The IPV Specialist also facilitates communication and coordination between IPV and Safety Officers.
Support IPV function with two-way communication with the Safety Officer network and GSPV functions, ensuring timely responses to queries, organization of meetings, production of written communication, etc. Coordinate routine tasks such as onboarding and offboarding activities for Safety Officers, PSMF updates, reconciliation, etc. Maintain the appropriate documentation necessary for IPV activities, such as Safety Officer contact details, nomination documents, procedural documents if applicable, etc. Participate and contribute to projects aimed at developing and implementing local and global PV processes which are both compliant with legislation and integrated into CSL's PV system. Support directly IPV Heads and Territory Managers with all other IPV-related activities as necessary.
This project will be looking to commence from January 2025 for 12 months. #J-18808-Ljbffr
