Are you a highly organised Project Manager with a passion for pharmaceutical development and scientific innovation?

At Remedica, we're looking for an ambitious R&D Project Manager to join our team on a 6-month fixed-term contract, starting in February. This is an exciting opportunity to play a pivotal role in driving the successful delivery of formulation and analytical development projects, working alongside talented scientists, analysts, and cross-functional teams in a dynamic pharmaceutical environment.

If you thrive on collaboration, enjoy bringing structure to complex projects, and are motivated by seeing innovative products progress from concept to reality, we'd love to hear from you.

About the Role

As an R&D Project Manager, you will be responsible for coordinating, facilitating, and monitoring the progress of pharmaceutical product development projects from initiation through to completion. You'll ensure projects remain aligned with agreed timelines, budgets, scope, and regulatory requirements while acting as the central point of coordination between internal teams and external partners.

This role offers excellent exposure across the full product development lifecycle and the opportunity to make a meaningful impact within a fast-paced R&D environment.

Key Responsibilities

You will:

• Coordinate the preparation and completion of project charters, including project scope, timelines, and cost parameters.
• Lead project kick-off activities, presentations, and stakeholder meetings.
• Monitor day-to-day project activities, milestones, and deliverables across formulation and analytical development teams.
• Collaborate with cross-functional departments to ensure projects are delivered on time and within budget.
• Track procurement and order status of materials, tooling, and development resources to maintain project timelines.
• Establish and manage development agreements with Contract Research Organisations (CROs), ensuring clear expectations around scope, budgets, and timelines.
• Monitor CRO performance, providing regular updates and escalating risks or delays when required.
• Oversee the progress of analytical method development, validation, and transfer activities.
• Track formulation development activities, scale-up processes, and validation batch execution.
• Manage project changes and communicate updates effectively to key stakeholders.
• Maintain accurate project documentation and communicate progress to R&D leadership.
• Prepare and present regular project status and progress reports.
• Update project management systems and departmental databases.
• Identify project risks and opportunities, proactively implementing mitigation plans and escalating concerns where necessary.

What We're Looking For

Essential Qualifications & Experience

• Bachelor's degree in Chemical Engineering, Chemistry, Pharmacy, or a related scientific discipline.
• Minimum 2 years' experience in a project management role.
• Strong organisational and stakeholder management skills.
• Excellent knowledge of Microsoft Office and project management systems.
• Strong communication skills in both Greek and English, written and verbal.

Desirable

• Master's degree in Pharmaceutical Sciences, Business Administration (MBA), or a related field.
• Project Management certification or relevant project management training.
• Experience within the pharmaceutical, life sciences, or regulated manufacturing sector.

Why Join Remedica?

At Remedica, innovation and collaboration are at the heart of what we do. This role offers the opportunity to work on a diverse portfolio of pharmaceutical development projects, gain exposure to cross-functional teams and external partners, and contribute to bringing high-quality medicines to patients around the world.

If you're looking for a challenging and rewarding opportunity where your project management expertise can make a real impact, we'd love to hear from you.

Apply today and help shape the future of pharmaceutical innovation at Remedica.