Clinical Project Manager

Purpose
Coordinate projects from development to product launch, coordinating the needs of all the involved departments (R&D, toxicology clinic records, production, quality, clinical operations, business development and sales) to streamline the development process, ensure that the times and budgets are under control and achieve a successful registration and launch of the product on the market.

Responsibilities

• Ensure the correct understanding of the needs of the development plan from strategy to detailed tasks by all the people involved.
• Analyze the needs of each project and design stages and milestones in calendar (scope, goals, schedule, timelines, quality, resources, etc.).
• Propose alternative or contingency solutions to changes or problems in implementation.
• Propose allocation of responsibilities and resources.
• Ensure optimization of resources (capital, effort, organization, departments, systems, etc.), time, cost and quality.
• Establish communication and control system (system of recording and reporting on project progress, deviations, shares, etc.).
• Track each phase in order to ensure the implementation of all actions to improve and ensure a high level of quality and compliance with the set standards.

Requirements

• Education: University Degree, preferred Pharmacy or similar. PhD in Pharmaceutical area. PMP training will be very valuable.
• Advanced English, knowledge of other languages will be an asset.
• 2/3 years of experience in project management in the pharmaceutical industry.

Skills

• Proactivity, leadership, communication skills, multitasking and global mindset to work with local and international teams, initiative to improve processes.