Descrizione dell'offerta
Overview
Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry leaders, ensuring the scientific value of our cardiovascular, thrombosis, and dyslipidemia products is understood. We connect, communicate, and train internal employees to ensure a thorough understanding of the science behind cardiovascular, thrombotic, and lipid disorders and review further unmet medical needs to support collaboration to further differentiate our portfolio.
Responsibilities
Engage in non‑promotional peer‑to‑peer exchange of medical and scientific information with Scientific Leaders or Key Decision Makers regarding cardiovascular disease, thrombosis, and dyslipidemia, to the extent permitted by law and local regulation.
Gain deep insights on cardiovascular disease and related thrombotic and lipid disorders, therapeutic area needs, data gaps, and challenges in their local geography.
Represent Medical Affairs at local or regional non‑promotional medical events and collaborate in the coordination of pre‑event scientific information and post‑event scientific summaries.
Respond to unsolicited requests for medical, scientific, pipeline, or marketed product information related to cardiovascular, thrombosis, and dyslipidemia therapies from Scientific Leaders or Key Decision Makers utilizing appropriate approved scientific materials.
Provide medical/scientific support, including written documentation and/or verbal interactions for Health Technology Assessments and formulary decisions, following the principles of scientific exchange.
Participate in the development and implementation of Medical Affairs Plans focused on cardiovascular disease, thrombosis, and dyslipidemia.
Support the identification of potential study investigators for sponsored studies in collaboration with Global Clinical Trials Organization, GDSA, or Center for Observational and Real World Research personnel.
Provide insights internally on scientific gaps, ideas, and other topics gathered from scientific exchange to inform our Investigator Study Program Areas of Interest, development programs, and company therapeutic area strategy.
Support company commercial colleagues by providing on‑label or disease state scientific training to our company personnel in the therapeutic area when requested and where allowed.
Geographic Working Area
Central‑Northern Italy:
Marche, Toscana, Umbria, Abruzzo, Liguria
Qualifications
An advanced scientific degree (MD, PharmD, or Ph.D. in a life science) is strongly preferred; a college degree in pharmacy is required.
Skills
Minimum of 2 years of pharmaceutical experience; experience in the cardiovascular / thrombosis / dyslipidemia therapeutic area is highly preferred.
Strong scientific baseline knowledge in cardiovascular disease, thrombosis, and dyslipidemia; clinical trial methods, implementation, and data interpretation; sound scientific and clinical judgment; and eagerness to learn more in‑depth about this specific therapeutic area.
Ability to present scientific and other technical information with confidence, engendering trust and credibility.
Excellent communication skills across a variety of internal and external audiences, including listening and probing skills.
Strong collaboration skills and ability to function within a team environment.
Ability to handle multiple tasks simultaneously and work under pressure.
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Responsibilities
Engage in non‑promotional peer‑to‑peer exchange of medical and scientific information with Scientific Leaders or Key Decision Makers regarding cardiovascular disease, thrombosis, and dyslipidemia, to the extent permitted by law and local regulation.
Gain deep insights on cardiovascular disease and related thrombotic and lipid disorders, therapeutic area needs, data gaps, and challenges in their local geography.
Represent Medical Affairs at local or regional non‑promotional medical events and collaborate in the coordination of pre‑event scientific information and post‑event scientific summaries.
Respond to unsolicited requests for medical, scientific, pipeline, or marketed product information related to cardiovascular, thrombosis, and dyslipidemia therapies from Scientific Leaders or Key Decision Makers utilizing appropriate approved scientific materials.
Provide medical/scientific support, including written documentation and/or verbal interactions for Health Technology Assessments and formulary decisions, following the principles of scientific exchange.
Participate in the development and implementation of Medical Affairs Plans focused on cardiovascular disease, thrombosis, and dyslipidemia.
Support the identification of potential study investigators for sponsored studies in collaboration with Global Clinical Trials Organization, GDSA, or Center for Observational and Real World Research personnel.
Provide insights internally on scientific gaps, ideas, and other topics gathered from scientific exchange to inform our Investigator Study Program Areas of Interest, development programs, and company therapeutic area strategy.
Support company commercial colleagues by providing on‑label or disease state scientific training to our company personnel in the therapeutic area when requested and where allowed.
Geographic Working Area
Central‑Northern Italy:
Marche, Toscana, Umbria, Abruzzo, Liguria
Qualifications
An advanced scientific degree (MD, PharmD, or Ph.D. in a life science) is strongly preferred; a college degree in pharmacy is required.
Skills
Minimum of 2 years of pharmaceutical experience; experience in the cardiovascular / thrombosis / dyslipidemia therapeutic area is highly preferred.
Strong scientific baseline knowledge in cardiovascular disease, thrombosis, and dyslipidemia; clinical trial methods, implementation, and data interpretation; sound scientific and clinical judgment; and eagerness to learn more in‑depth about this specific therapeutic area.
Ability to present scientific and other technical information with confidence, engendering trust and credibility.
Excellent communication skills across a variety of internal and external audiences, including listening and probing skills.
Strong collaboration skills and ability to function within a team environment.
Ability to handle multiple tasks simultaneously and work under pressure.
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
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