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Pharmacovigilance (Project) Manager

Role overview

Qualifications

  • Life science degree
  • 5-year experience in Pharmacovigilance, including case processing
  • Experience with end-to-end case processing of clinical trials
  • Fluent English

Responsibilities

  • 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
  • Manage and track assigned projects invoices

Key facts

Other skills

  • Communication
  • Organizational Skills
  • Time Management
  • Teamwork

About the company

Biomapas logo

Biomapas

Contract Research Organizations (CRO)

Biomapas is a functional and full outsourcing solution provider to the global life science industry. As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle. Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success. We keep our promises. Always. Social media privacy policy: bit.ly/privacy-biomapas

Company details

Company typeSME
IndustryContract Research Organizations (CRO)
Company size201 - 500

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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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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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