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Pharmacovigilance (Project) Manager (Veeva Safety experience required)

Key Facts

Remote From: 
Category:  M&A Manager
Full time
Senior (5-10 years)
English

Other Skills

  • •
    Microsoft Office
  • •
    Communication
  • •
    Time Management

Roles & Responsibilities

  • Life science degree
  • 5-year experience in Pharmacovigilance, including case processing
  • Experience with end-to-end case processing of clinical trials
  • Veeva Vault handling mandatory

Requirements:

  • 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

Job description

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

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