MENARINI GROUP

High quality therapeutics and diagnostics solutions for patients, ethics as our underlying principle, dedication to innovation and advancement, strong people centricity and environmental sustainability.

These five pillars form the foundation of the Menarini Group, an Italian pharmaceutical company with more than 135 years of history. Founded in 1886 in Naples under the name of Farmacia Internazionale, in 1915 Menarini moved to Florence where the Group’s headquarters are still located today.

The Menarini Group is present in 140 countries around the world. Its companies span from Europe to Asia, to Africa and the Middle East, to Central America and to the United States where with the acquisition of Stemline Therapeutics, a NASDAQ-listed biopharmaceutical company, the company marked its entry into the US oncology market.

Thanks to the valuable contribution of over 17,000 employees, every year more than 500 million packs of drugs are produced at the Group's 18 manufacturing sites including a biotech plant for the manufacturing of monoclonal antibodies that also serves external clients. Our drugs are distributed across 6 continents for the treatment of pathologies in cardiology, oncology, pneumology, inflammation and gastroenterology.

Menarini invests in the future and guarantees drug availability in the present for the improvement of patient health and well-being.

In its 9 Research & Development centers, Menarini’s main focus is dedicated to therapeutic areas with unresolved pathologies, such as oncology and anti-infectives (AMR), where increasing treatment options is fundamental to helping those in need. The Group's pipeline concentrates on innovative drugs and technologies including both small molecule and biologics for hematologic and solid tumors for greater personalized solutions.

The Group has also invested in diagnostics to develop instruments with high speed and precision for diagnoses in various fields such as clinical chemistry, diabetes, immunology, hematology, histology and point-of-care. In addition, Menarini is developing advanced technologies for the analysis of rare tumor cells with single cell precision.

From research to manufacturing, from distribution to scientific information, Menarini's goal is to achieve excellence.

Medical Assessor - Global PharmacoVigilance (GPV)

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POSITION TITLE: Global PharmacoVigilance (GPV) Medical Assessor

REPORTS TO: GPV Risk Evaluation Unit Manager (and, functionally, to GPV Director / EUQPPV)
BASED: Florence
EXPECTED TRAVEL: Occasional

CONTEXT
The candidate will join the Global PharmacoVigilance (GPV) department within the Risk Evaluation Unit (REU) team. The GPVREU team is in charge of supporting the GPV Director / EU Qualified Person for PharmacoVigilance (EUQPPV) for the activities related to the benefit-risk profile assessment of Menarini medicinal products.

MAIN ACTIVITIES AND RESPONSIBILITIES
In the frame of the GPV Department, being familiar with the EU and non-EU PV legislation and requirements, the ideal candidate will be involved in several activities such as:

Review of international scientific literature for the assigned medicinal products.
Signal detection and management for the assigned medicinal products.
Providing Medical support in writing and reviewing Aggregate Safety Reports such as Periodic Benefit-Risk Evaluation Reports, Development Safety Update Reports, Addendum to Clinical Overview, Risk Management Plans.
Supporting other Units within GPV (e.g. for Triage and Medical Review of Individual Cases Safety Reports).
Supporting other Departments (i.e. Regulatory Affairs, Medical Directions, etc.) for preparation of the safety sections of documentation for Marketing Authorisation application or renewal of concerned medicinal products.
Supporting the GPVREU Manager and GPV Director in ensuring the harmonisation of the SmPC safety sections across the Company territories.
Supporting the GPVREU Manager and GPV Director in ensuring that any request from the Competent Authorities concerning the benefit/risk profile of a medicinal product is answered fully and promptly.

The mentioned activities require interactions with several internal stakeholders both at Global (Regulatory Affairs, Medical, Marketing, Scientific Service, PV) and Affiliate level (PV), as well as external consultants.

JOB REQUIREMENTS

Education: Master’s Degree in Medicine and Surgery (mandatory); Specialization, preferably in Pharmacology, Epidemiology, Medical Statistics, Internal Medicine, General Medicine (or equivalent branches, i.e. Cardiology, Neurology, Infectivology, Oncology, etc.), Hygiene and Preventive Medicine (or equivalent branches).
Years of experience: Previous experience in pharmaceutical industry (PharmacoVigilance preferred).
Qualification and skills: precision, timeliness, good organisation skills, teamwork, knowledge of pertinent medical or pharmaceutical and clinical practice, confidence with electronic tools (MSOffice).
Language skills and level of proficiency: English intermediate (minimum, as all work documentation and most of the communication shall be carried out in English), good written and verbal communication skills.

Ti senti la persona giusta per questa posizione?
📩 Candidati online nella settimana dal 16 al 22 giugno.

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Medical Advisor

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POSITION TITLE: Medical Advisor

REPORTS TO: Corporate Therapeutic Area Manager
BASED: Florence
EXPECTED TRAVEL: 40 %

CONTEXT
Corporate Medico-Marketing Team is a cross-functional team with the primary objective to support Menarini in implementing Corporate Products business plans and in commercial/medical evaluation of future opportunities. The Corporate Medical Advisor, inside the Corporate Medico-Marketing Team, reports to Therapeutic Area Manager and works closely with the Corporate Product Manager. Other internal relationships include relations with Medical Affairs, Regulatory and Legal personnel. External relationships include relations with medical Advisors from affiliated Companies and Partners, Scientific Societies, KOL etc.

MAIN ACTIVITIES AND RESPONSIBILITIES

Cooperate with Product Manager in developing of the medical component of the brand strategy.
Develop and execute medical affairs & publication plans for the products in synergy with Medical Affairs dep.
Manage clinical trial in cooperation with Medical Affairs dep.
Develop a proper advocacy plan and engage with international Key Opinion Leader.
Release products scientific training to both affiliates and partners.
Create and review promotional materials.
Cooperate with other Departments (Regulatory/Market-Access/Pharmacovigilance) in the preparation of relevant documents necessary to meet the requirements of international/local
Health Authorities.
Medical enquiries management.
Support/investigate life cycle management initiatives for the products.
Support Business Development in the assessment of new products evaluation.

JOB REQUIREMENTS

Bachelor’s degree in Medicine.
1 year of previous experience in a medical position is preferred.
Fluent English in written and verbal format.
Optimal use of Microsoft Office (PowerPoint, Excel and Word).
Excellent communication and public speaking skills.
Excellent relational and organizational skills.

Ti senti la persona giusta per questa posizione?
📩 Candidati online nella settimana dal 16 al 22 giugno.

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Medical Manager

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POSITION TITLE: Medical Manager

REPORTS TO: MEDICAL AFFAIR DIRECTOR
BASED: FLORENCE
EXPECTED TRAVEL: UP TO 30 %

CONTEXT
The Medical Affair Team has the primary objective to support he scientific information and development on the Menarini products The Medical Manager works closely with the Product Manager. Other internal relationships include relations with MSL Lead, Pharmacovigilance and Regulatory personnel. External relationships include MSLs, Medical Reps, Corporate Medical Managers, Scientific Societies, KOLs.

MAIN ACTIVITIES AND RESPONSIBILITIES

Cooperate with Product Manager in developing of the medical component of the brand strategy.
Develop and execute medical affairs plan for the products
Manage clinical trials in cooperation with Corporate Medical Affairs department, in the role of LOCAL Study Medical Expert.
Develop a proper advocacy plan and engage with national Key Opinion Leader.
Support MSLs in the execution of the local medical plan
Release scientific trainings to medical reps and MSLs.
Create and review promotional materials.
Cooperate with other Departments (Regulatory/MarketAccess/Pharmacovigilance) in the preparation of relevant documents necessary to meet the requirements of local Health Authorities.
Medical enquiries management.
Support/investigate life cycle management initiatives for the products.