The Medical Affairs Manager, Italy coordinates medical leadership within DePuy Synthes orthopaedic portfolio in Italy, collaborating with cross‐functional teams to advance patient care and clinical outcomes.
Aumenti le sue possibilità di ottenere un colloquio leggendo la seguente panoramica di questo ruolo prima di candidarsi. Key Responsibilities
* Serve as the primary medical and scientific expert for assigned orthopedic products and therapeutic areas in Italy.
* Develop and execute local medical affairs plans aligned with global and regional strategies.
* Provide medical input into clinical studies, post‐market surveillance, and real‐world evidence activities.
* Support investigator‐initiated studies and collaborative research in compliance with company policies and local regulations.
* Deliver high‐quality scientific exchange and education to healthcare professionals, including presentations and advisory boards.
* Partner with Regulatory, Quality, Marketing, and Commercial teams to ensure accurate, compliant medical content and product communication.
* Review and approve medical materials to ensure scientific accuracy and regulatory compliance.
* Monitor medical trends, clinical literature, and competitive activity to inform strategy and decision‐making.
Qualifications
* Education Required: Advanced degree in a scientific or healthcare discipline (e.g., MD, PharmD, PhD, MSc in Life Sciences or related field).
* Preferred: Medical degree (MD) or doctorate with specialization relevant to orthopedics or medical devices.
* Experience and Skills Required (6–8 years):
o Experience in Medical Affairs, Clinical Affairs, or a related scientific role within medical devices or pharmaceuticals.
o Demonstrated knowledge of clinical research, evidence generation, and medical compliance standards.
o Experience engaging with healthcare professionals and key opinion leaders in a scientific, non‐promotional manner.
o Strong analytical, communication, and presentation skills.
o Ability to work effectively in cross‐functional, matrixed environments.
o Solid understanding of local (Italian) healthcare systems and regulatory requirements.
* Preferred (orthopedics, trauma, sports medicine, related surgical specialties):
o Prior involvement in clinical trial management or post‐market clinical follow‐up.
o Experience supporting product launches or lifecycle management from a medical affairs perspective.
o Familiarity with European medical device regulations and clinical evaluation requirements.
o Leadership experience mentoring junior medical or clinical colleagues.
* Fluency in Italian and English (written and spoken) is required.
* Up to ~30% domestic travel within Italy; limited international travel as needed.
* Relevant clinical or research certifications are a plus.
* Valid driver's licence required for field engagement. xrdztoy
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.
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