Celltrion Group provides biosimilar and innovative biopharmaceutical medications to help increase patient access to advanced therapies around the world.
Celltrion Group offers biologics to about 110 countries, along with more than 30 global partners around the world. With hands-on experience and knowledge accumulated through years of working in the advanced pharmaceutical markets around the world, Celltrion Group has been securing distribution channels and providing patients with biosimilars at affordable prices.
We are searching for highly motivated Pharma Product Specialist with a good scientific background and a previous experience in a similar role to join our Sales Department.
Celltrion Healthcare Italy is a rapidly developing company with a strong product pipeline across multiple therapeutic areas.
Candidates should have 3 years of previous experience in Specialty drugs, but attitude will be the first driver for our choice. The ideal ones are team builder, proactive, flexible and open-minded, with an energetic and result-oriented attitude, highly motivated to contribute to the growth and to grow with our Company in Italy.
Key responsibilities:
- Support Area Manager understanding of assigned region(s)
- Design, together with Area Manager and Medical Liaisons, a map of biologics prescribing physicians
- Promote, in accordance with guidelines from Regional Business Manager, Celltrion products to physicians
- Map and build a relationship with all stakeholders that can impact access and distribution of Celltrion products in the assigned area – including administrative personnel, pharmacists, physicians
- Monitor local policies and commercial actions/projects of competition, report to Regional Business Manager and design potential actions to take
- Keep accurate tracking of activities done and planned, in accordance with RBM requests and provided tools (CRM)
- Present appropriately Celltrion products and their value proposition in light of sustainability of the healthcare system, using materials supplied by the Italian Office
- Identify, in alignment with Commercial and Medical, potential commercial opportunities within the private Health sector and support negotiations with their procurement offices
- Ensure legal compliance to all applicable local rules and regulations, in alignment with applicable law and Celltrion code of conduct
- Appropriately report all activities done in field, including personal interactions, materials distribution, expenses incurred
Essential requirements:
- Scientific Degree in medicine, pharmacy, biology or equivalent;
- Master in pharma market access (best but not mandatory);
- Good English, Italian native speaker;
- Pharma sector previous experience as a Product Specialist;
- Previous experience in IBD or Rheumatoid Arthritis or Psoriasis Arthritis;
- Deep knowledge of assigned region(s) process and stakeholders;
- Excellent sales and negotiation skills, with result-oriented attitude;
- Availability to travel more than 50% of the time, including overnight stays;
- Experience in product launches (best but not mandatory);
Workplace: South Italy
Skills Required
- Scientific degree in medicine, pharmacy, biology or equivalent
- Minimum 3 years' experience in specialty drugs
- Previous experience as a Pharma Product Specialist
- Previous experience in IBD, Rheumatoid Arthritis or Psoriasis Arthritis
- Deep knowledge of assigned region(s) processes and stakeholders
- Excellent sales and negotiation skills, result-oriented attitude
- Good English and Italian native speaker
- Availability to travel more than 50% of the time, including overnight stays
- Master in pharma market access
- Experience in product launches
What We Do
Celltrion is a leading global biopharmaceutical company headquartered in Incheon, South Korea. It specializes in the research, development, manufacturing, marketing, and sales of biosimilars and innovative therapeutics. The company is dedicated to improving patient access to advanced medications through its fully integrated model, which encompasses the entire process from research and development to clinical trials, regulatory affairs, production, and global distribution.
