Operates as a global CRO with projects spanning over 60 countries, providing a highly international work environment.
Frequently recruits for specialized roles requiring multiple languages, such as Japanese-speaking Pharmacovigilance Specialists.
Offers remote and hybrid work arrangements for many of its clinical and regulatory positions in Spain.
Provides a platform for professionals to work on diverse therapeutic areas and international clinical trials.

Pharmacovigilance (Project) Manager

Biomapas

Requirements

Life science degree 5-year experience in Pharmacovigilance, including case processing Experience with end-to-end case processing of clinical trials Oncology background preferred. Veeva Vault handling mandatory Fluent English Excellent knowledge of international regulations (ICH, EU GVP Modules) Strong computer literacy with intensive experience with safety data bases and MS Office Demonstrated ability to set up and implement drug safety strategies, develop PV related procedures, elevate and resolve issues Strong communication, organizational and time management skills Ability to work independently and in a team

Benefits

Professional growth and career opportunities
International team and environment
Rewarding business referral policy
Employee referral policy
Flexible working hours, remote working

Original Advert

Join global Pharmacovigilance team of Biomapas Group as a Pharmacovigilance (Project) Manager (Veeva Safety experience required)

Pharmacovigilance (Project) Manager is responsible for assuring compliance with Quality Management System, overseeing a team of PV professionals and the project financials, and building long term relations with clients.

Position is in any EUCountry

Responsibilities

To oversee and manage strategic/key accounts
Maintain high quality regular communication with Clients contact persons
Ensure high quality performance of activities in scope through effective liaising with Biomapas staff responsible for PV regional management
Effectively manage a team supporting project management activities
Manage and track assigned projects invoices
Oversee project financials and profitability
Support in developing project management process
Support in preparations and attendance of bid defences
Involve in forecasting and project budgeting
Support team with issue resolution and workflow distribution

Requirements

Life science degree
5-year experience in Pharmacovigilance, including case processing
Experience with end-to-end case processing of clinical trials
Oncology background preferred.
Veeva Vault handling mandatory
Fluent English
Excellent knowledge of international regulations (ICH, EU GVP Modules)
Strong computer literacy with intensive experience with safety data bases and MS Office
Demonstrated ability to set up and implement drug safety strategies, develop PV related procedures, elevate and resolve issues
Strong communication, organizational and time management skills
Ability to work independently and in a team

Benefits