Director, Medical Affairs
Ptc Therapeutics
ph3Director, Medical Affairs /h3 pAzienda : Ptc Therapeutics Tipo Lavoro : Full Time Italy /p h3Descrizione Lavoro - Director, Medical Affairs /h3 pPTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life’s moments for children and adults living with a rare disease. /p pAt PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our teamb, /bfostering a strong sense of belonging. /p pVisit our website to learn more about our company and culture! Site: /p h3Job Description Summary: /h3 pThe Director, Medical Affairs is responsible for providing strategic and operational leadership to the Medical Affairs function for the respective country or region of responsibility to support marketed and pipeline products. The incumbent is responsible for adapting global and regional medical affairs strategies to ensure that it is fit for purpose at the local/regional level. /p pThe Director, Medical Affairs supports and represents PTC and its products with, and to, key opinion leaders (KOL's), clinicians, academic institutions, and professional organizations within the assigned country or region. He/she addresses the specific needs of these clients by responding to unsolicited requests for information about PTC marketed and developing products. /p h3Job Description: /h3 pbResponsibilities of the role include: /b /p ul liAdapts and influences the global, regional and country medical affairs strategy required in the country or region of responsibility. /li liManages, coaches and mentors a direct report /li liResponsible for interactions with local authorities, local key opinion leaders (KOLs) and payers, patient organizations as well as other external stakeholders. /li liEnsures execution of medical affairs strategy and builds and maintains trusted medical/scientific relationships with health community stakeholders. /li liCollaborates with Marketing to ensure that the local strategic medical affairs plans are in line with the marketing plans/brand strategies. /li liDrives the tactical implementation of medical affairs plans across the country, including but not limited to: KOL development and relationship building as well as the building of the scientific communications platform (publications, congresses etc.) and other related projects. /li liReviews promotional and non-promotional materials with particular regard to medical accuracy and compliance to local regulation and code of practice. /li liManages and directs medical information process and service in close collaboration with other functions in medical affairs. /li liIdentifies local thought leaders, engages in scientific exchange and develops rapport with experts in the therapeutic area. /li liIdentifies, organizes and carry out regional medical initiatives (i.e. leads medical discussions at national advisory board meetings). /li liProvides training and scientific education to commercial, medical teams and other internal stakeholders /li liProvides support in the administration of clinical trials on request by Clinical Development teams; collaborates and provides support to other departments, especially to Regulatory Affairs and Pharmacovigilance (PV); represents Global Medical Affairs at local, regional and international scientific congresses. /li liPerform other tasks and assignments as needed and specified by management. /li /ul pbRequirements for the role include: /b /p ul liAn advanced degree (e.g., Masters, PharmD, M.D. or Ph.D.) in a scientific discipline and demonstrated experience of progressive responsibility in, pharmaceutical, biotechnology or related environment with a minimum of 6 years medical affairs experience or equivalent combination of education and experience. /li liPeople management experience is a must. /li liDemonstrates leadership and the ability to manage and coach direct reports /li liHands-on experience supporting the registration and launch of an orphan, rare disease, and/or specialized drug(s) in the country/region of responsibility. /li liIn-depth, hands on experience working with KOL's, clinicians, HCPs, payors, and/or academic institutions establishing/maintaining relationships and scientific/medical credibility. /li liDemonstrated success in interpreting scientific data and presenting research information to scientists and HCPs. /li liExperience dealing with the local regulatory authorities and payor organizations. /li liIn-depth experience adapting regional plans to a country orientation, while working within a global framework. /li liExcellent working knowledge in local regulations and codes of practice as well as a good understanding of the market and medical dynamics in the designated territory. /li liAbility to influence without direct authority. /li liProficiency with Microsoft Office. /li liExcellent verbal and written communication and skills, including scientific/technical writing and presentations with the ability to communicate complex technical information clearly. /li liAbility to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members. /li liAnalytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines. /li liExcellent planning, organization and time management skills including the ability to support and prioritize multiple projects. /li liDemonstrates leadership and the ability to manage and coach direct reports. /li liFluent in Italian and English (written and verbal). /li /ul p* Travel requirements. /p pFlexibility to travel domestically and internationally as needed by the business /p h3EEO Statement: /h3 pPTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination. /p h3Informazioni sull'azienda /h3 pPtc Therapeutics /p pPTC Therapeutics pioneers pharmaceutical science to transform lives and treat rare diseases, like Duchenne Muscular Dystrophy, Spinal Muscular Atrophy, Huntington's Disease, Leukemia, and more. /p /p #J-18808-Ljbffr
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