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

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