Main duties & key responsibilities:
- Coordinate and monitor R&D projects, ensuring delivery within scope, time, and budget.
- Develop, update, and track the R&D development plan, identifying potential delays and proposing corrective actions.
- Serve as a communication hub between internal teams (R&D, Regulatory Affairs, CMC, and external stakeholders (CDMOs, CROs, suppliers).
- Support dossier preparation and submission activities by aligning all relevant teams and timelines.
- Coordinate Bioequivalence studies, including partner selection, documentation review, and logistics.
- Liaise with IP attorneys to identify and manage patent-related issues during development.
- Maintain accurate project documentation and ensure smooth information flow across all functions.
- Implement best practices to enhance project performance and efficiency.
Requirements:
- Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering, or a related field.
- Minimum 1 year of experience in the pharmaceutical industry, preferably in R&D, project management, or regulatory-related roles.
- Good understanding of pharmaceutical regulations and development processes.
- Excellent communication, organizational, and problem-solving skills.
- Ability to work collaboratively in a fast-paced, cross-functional environment.
- Proficiency in English (oral and written).
Benefits:
- Competitive remuneration package, including benefits
- Ability to become part of one of the most dynamic and prospective teams in the Pharmaceutical industry in Greece
- Continuous opportunities in advancing personal and career goals
To apply, kindly submit your CV at HR@PharmaPath.eu referencing the code PROM/10.
Based on your consent all received applications will be stored in our database for maximum 6 months and all data will be treated with strict confidentiality commensurate to data protection regulation.
