# Medical Information/Pharmacovigilance Project Manager

**Company:** [Biomapas](https://jobs.workable.com/companies/8iejh2fCgUzZGK2eUKBree.md)
**Location:** Remote
**Workplace:** remote
**Employment type:** Full-time

[Apply for this job](https://jobs.workable.com/view/1dcb89e0-2b4a-46f1-a823-00f72034e997)

## Description

### Join our global Pharmacovigilance and Medical Information department as a Medical Information/Pharmacovigilance Project Manager.

**Medical Information/Pharmacovigilance Project Manager** ensures compliance with the Quality Management System, coordinates project activities, oversees project financials, and fosters long-term client relationships.

_Position applicable only for EU countries. All CV's must be submitted in English language for assessment._

### Responsibilities:

-   Oversee Medical Information and Pharmacovigilance service delivery, including medical inquiry handling and response management, safety information intake and reporting, quality oversight, and compliance with applicable procedures and timelines
-   Act as the primary contact point for project-related matters for the client and internally, and manage client accounts
-   Ensure high quality performance of activities in countries in scope through effective liaising with Biomapas staff responsible for PV/MI regional management
-   Coordinate and support the implementation, maintenance, and optimization of Medical Information databases and inquiry management systems
-   Ensure appropriate oversight of operational metrics, reporting, and service-level agreements (SLAs)Oversee PV/MI projects’ financials and profitability, forecasting and project budgeting
-   Support in developing project management process
-   Support in preparations and attendance of bid defenses

## Requirements

-   University degree in the Life Science field
-   At least 5-year experience in Pharmacovigilance and/or Medical Information Project Management experience from ideally a service provide / CRO
-   Strong knowledge of Medical Information processes, including medical inquiry handling, scientific response management, documentation, and quality requirements.
-   Hands-on experience with Medical Information databases, inquiry management systems, or related MI technology platforms is highly preferred.
-   Fluent English
-   Excellent knowledge of international regulations (ICH, EU GVP Modules)
-   Excellent client-facing skills including strong communication and presentation skills
-   Strong computer literacy with intensive experience with safety databases and MS Office
-   Demonstrated ability to set up and implement drug safety strategies, develop PV/MI 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
-   Personal accident and business trip insurance
-   Additional health insurance
-   Remote/home based
-   Rewarding referral policy
-   Workplace establishment allowance (fully remote)
-   Team building, global meetings