Medical Information Specialist & PV Monitor

Celltrion Healthcare Italia; Milano; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company based in Milan is looking for a Medical Information Specialist & PV Monitor. This role involves providing scientific and medical information about products to healthcare professionals and managing pharmacovigilance activities, including adverse event reporting and compliance. Candidates are expected to have a scientific background, fluency in English, and preferably experience in the pharmaceutical industry. An organizational mindset with attention to detail is essential, as well as the ability to work in a fast-paced environment.

Competenze

• Previous experience (at least two years) in a similar role.
• Knowledge and experience in Rheumatology, Gastroenterology, Oncology, Hematology, and related fields.

Mansioni

• Provide accurate medical information regarding products to healthcare professionals.
• Collect and report adverse events and safety information.
• Monitor scientific literature and develop medical information materials.
• Support training on pharmacovigilance for new employees.

Conoscenze

Fluency in English

Excellent organizational skills

Analytical skills

Ability to work independently

Formazione

Scientific degree (medicine, pharmacy, biology)

PhD or master's program

Descrizione del lavoro

Medical Information Specialist & PV Monitor

We are searching for a brilliant Medical Information Specialist & PV Monitor with a strong scientific background and a previous experience (at least two years) in a similar role to join our Medical Affairs Department.

Responsibilities

The new colleague will be responsible for providing accurate, balanced, and evidence-based scientific and medical information regarding Celltrion’s products to healthcare professionals (HCPs) and internal stakeholders, and for the collection and reporting of adverse events (AEs) serious and non‑serious and other safety information related to the company’s medicinal products.

Medical Information Specialist Responsibilities

• Answer medical and scientific inquiries from healthcare professionals and internal teams in a timely and compliant manner;
• Develop and maintain standard response letters and other medical information materials;
• Monitor scientific literature and ensure that responses and materials reflect the latest evidence and clinical data;
• Participate in cross‑functional projects within Medical Affairs;
• Contribute to internal scientific training for field‑based and office colleagues;
• Participation in advisory boards and round tables for the creation of reports (if necessary);
• Ensure proper reporting and follow‑up of adverse events and product complaints in collaboration with the Pharmacovigilance department;
• Support the medical review of promotional and non‑promotional materials for scientific accuracy and regulatory compliance;

Pharmacovigilance Monitor Responsibilities

• Collect, review, and assess individual case safety reports (ICSRs) from healthcare professionals, clinical trials, and literature;
• Collaborate with external offices for all activities related to PV and local reconciling activities;
• Assist in the preparation of Risk Management Plans (RMPs);
• Collaborate with Medical Affairs, Regulatory, and Quality departments for cross‑functional safety activities;
• Support audits and inspections related to pharmacovigilance processes and documentation;
• Maintain up‑to‑date knowledge of global pharmacovigilance regulations (e.g., EMA, FDA, MHRA);
• Ensure internal scientific training on PV for all new employees;

Qualifications

• Scientific degree (medicine, pharmacy, biology or equivalent);
• Achievement of PhD and/or master program (preferred but not mandatory);
• Fluency in English;
• Deep understanding of all biology and medicine related aspects of the therapeutic areas assigned;
• Experience in the pharmaceutical industry, preferably in a medical role (Medical Info & Pharmacovigilance) in a pharmaceutical company in Italy (preferred but not mandatory);
• Knowledge and experience in Rheumatology, Gastroenterology, Oncology, Hematology, Allergology, Pneumology, biological/biosimilar drugs (preferred but not mandatory);
• Ability to work independently and in cross‑functional teams in a fast‑paced environment;
• Excellent organizational and analytical skills with attention to detail.

Workplace

Milan, office based