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
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
Key team members
Tomaz Trcek
Martijn van de Leur
Valdis Tocs
Inga Garliauskiene
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