For a leading Greek pharmaceutical company.
Responsibilities
- Lead and coordinate R&D projects, ensuring timely delivery within scope, budget, and quality requirements.
- Collaborate with cross-functional teams (R&D, Regulatory Affairs, Supply Chain, Quality, and external partners) to support successful project execution.
- Develop, monitor, and maintain project plans, timelines, milestones, and development trackers, proactively identifying risks and implementing corrective actions when needed.
- Support the preparation, monitoring, and control of the R&D budget, ensuring alignment with financial targets and development priorities.
- Coordinate interactions with external stakeholders, including API suppliers, CDMOs, CROs, and other development partners.
- Monitor regulatory submission, dossier preparation, approval, and launch timelines to ensure projects progress according to plan.
- Support portfolio evaluation activities by contributing to project feasibility assessments, development strategies, and business case analyses.
- Coordinate intellectual property (IP) activities and patent-related assessments in collaboration with external patent advisors and internal teams.
- Drive continuous improvement by implementing best practices and lessons learned across development projects.
Requirements
- Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering, or a related scientific field.
- Minimum 2 years of experience in project coordination, project management, or a similar role within the pharmaceutical industry.
- Good understanding of pharmaceutical development processes and relevant regulatory requirements.
- Strong organizational, planning, and time management skills, with the ability to manage multiple projects and deadlines simultaneously.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders.
- Proficiency in Microsoft Office applications, particularly Excel and PowerPoint.
- Excellent command of the English language, both written and spoken.
- Experience in pharmaceutical product development, dossier submission processes, Bioequivalence studies, or technology transfer projects will be considered an asset.
Benefits
- Competitive remuneration package.
- Annual performance bonus based on company and individual objectives.
- Private health insurance.
- Ongoing training and professional development opportunities.
- Career development opportunities within a growing pharmaceutical company with an international presence.