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
Skills Required
- 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 experience in safety databases and MS Office
- Demonstrated ability to set up and implement drug safety strategies
- Strong communication, organizational and time management skills
- Ability to work independently and in a team
What We Do
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
