Italy onlyAbout Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members who embody these values.
Position Overview:
The Medical Science Liaison (MSL) will serve as the scientific expert supporting the scientific and clinical interests of Krystal Biotech by interacting with healthcare professionals (HCPs) and key opinion leaders (KOLs) across the entire Italian territory. The MSL will play a pivotal role in ensuring that external stakeholders are informed about the latest scientific data, clinical studies, and medical developments related to Krystal products.
The MSL must possess strong scientific and clinical acumen, have a strong interest in emerging treatment modalities,excellent communication skills, the ability to build relationships within the medical community, and a true passion to help bring innovative medicines to patients with rare diseases.
Key Responsibilities:
- Serve as a scientific resource for KOLs, HCPs, and other external stakeholders by providing in-depth, non-promotional, and objective information about Krystal’s products, clinical trials, and research.
- Develop deep scientific expertise in dermatology, gene therapy, and rare diseases. Be the subject matter expert in this therapeutic area in the assigned region.
- Provide scientific presentations and educational sessions on disease states, clinical research, and new product developments to healthcare professionals and medical organizations.
- Establish and maintain strong relationships with KOLs, physicians, and academic institutions in Italy, acting as a key point of contact for scientific discussions and data dissemination.
- Provide timely education, data dissemination, and respond to unsolicited requests for medical information based on approved material within regulatory guidelines.
- Provide comprehensive education about VYJUVEK® when requested by HCPs, following up to answer questions related to gene therapy, including preparation and administration, together with product-related wound management.
- Identify and prioritize key stakeholders consistent with the therapeutic area medical plan to build value-based partnerships with HCPs.
- Gather data, generate insights, and provide feedback to the organization to deepen understanding of unmet needs and opinions of external stakeholders to contribute to the enhancement of Krystal Biotech’s scientific messages and strategy.
- Stay up to date on the latest scientific literature, competitor activities, and relevant developments in the therapeutic area. Disseminate key information to internal teams, including Medical Affairs, Commercial, and Regulatory Affairs.
- This position will play an important self-starter role in helping establish Krystal Biotech Medical presence at relevant scientific congresses, advocacy group events, gene therapy network events, helping execute on the strategic medical plan and buildout for Italy.
- Ensure that all interactions and communications with HCPs and external stakeholders comply with Italian regulatory guidelines and company policies, including transparency and ethical standards.
- Advanced degree in life sciences (PharmD, PhD, MD) or related field.
- Minimum of 3-5 years of experience in Italy as a Medical Science Liaison or in a related scientific or clinical role in the pharmaceutical or biotechnology industry.
- Dermatology, rare diseases, or advanced therapy medicinal products experience is highly relevant for therole.
- Strong understanding of the therapeutic area and the ability to engage in scientific discussions with KOLs and HCPs.
- Launch experience in Italy preferred.
- Excellent interpersonal and communication skills, with fluency in both Italian and English.
- Strong presentation skills with the ability to explain complex scientific concepts to diverse audiences.
- Ability to build and maintain relationships with KOLs and healthcare professionals.
- Strong organizational and project management skills, with the ability to work independently.
- In-depth knowledge of clinical trial design and clinical research methodologies.
- High level of scientific literacy and the ability to analyze and interpret clinical and preclinical data.
Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.
Privacy Policy:
Krystal Biotech collects your personal data to process your application and possibly offer you an employment contract. You have the right to access, rectify, erase, and obtain the portability of your personal data. Under certain conditions, you also have the right to restrict the processing and object to it. In order to reach out for new opportunities, and unless you object to it, this information will be kept for a maximum of 2 years if your application is unsuccessful. For more information on the use of your data and your rights, please consult our privacy policy.
United States
