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Pharmacovigilance Project Manager

Key Facts

Remote From: 
Category:  Project Manager
Full time
Senior (5-10 years)
English

Other Skills

  • •
    Communication
  • •
    Time Management
  • •
    Teamwork
  • •
    Problem Solving

Roles & Responsibilities

  • Life science degree
  • 5-year experience in Pharmacovigilance
  • Experience with end-to-end case processing of clinical trials
  • Oncology background preferred

Requirements:

  • To oversee and manage strategic/key accounts
  • Maintain high quality regular communication with Clients contact persons
  • Ensure high quality local performance of countries in scope through effective liaising with Biomapas staff responsible for PV regional management
  • Effectively manage a team supporting project management activities

Job description

Join Biomapas Group (DeltaPV) global Pharmacovigilance team as a Pharmacovigilance Project Manager.

Pharmacovigilance Project Manager is responsible for assuring compliance with local Quality Management System, delegating tasks employees delegated on the project, overseeing project financials, building long term relations with clients.

Position is in any European Country

Responsibilities

  • To oversee and manage strategic/key accounts
  • Maintain high quality regular communication with Clients contact persons
  • Ensure high quality local performance of countries 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
  • Experience with end-to-end case processing  of clinical trials
  • Oncology background preferred.
  • Veeva Vault handling preferred
  • 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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