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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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Lavora con Noi

Amgen Italia è un’azienda giovane e inclusiva, focalizzata sullo sviluppo delle persone, sulla valorizzazione delle loro potenzialità e del loro benessere, che si esprime in diversi ambiti, tra i quali naturalmente l’eguaglianza di genere. Lo confermano certificazioni importanti come il Great Place to Work e il Bollino Rosa. 

Inoltre, Amgen mette a disposizione dei propri dipendenti una serie di servizi e di iniziative finalizzati al loro benessere e ad assicurare un efficace work-life balance così da consentire una migliore gestione della vita privata e favorire l’equilibrio delle esigenze lavorative con quelle personali.

Amgen valorizza le giovani generazioni: circa un quarto dei dipendenti appartiene infatti alla generazione dei millennial e successive.

La Nostra Direzione Medica

All’interno della Direzione Medica di Amgen troviamo diversi profili:
♦︎ All’interno delle aree terapeutiche operano i Medical Advisors (con ruolo di sede) e i Medical Science Liaisons (con ruolo di territorio);
♦︎ Gli altri team della Funzione si occupano di Medical Information and Scientific Communications, Project Management e Compliance.

Chi Cerchiamo

♦︎ Cerchiamo candidati con esperienza clinica o scientifica (es. da esperienza di dottorato o di laboratorio), che abbiano una conoscenza approfondita delle nostre aree terapeutiche.
♦︎ Il candidato ideale è curioso, motivato e determinato in quello che fa. Si rispecchia nei nostri Valori e vuole mettersi in gioco, raggiungendo gli obiettivi insieme al suo team.
♦︎ Cerchiamo dei profili appassionati delle aree terapeutiche che copriamo in Italia*: Chronic Disease (cardiologia, malattie infiammatorie, osteoporosi, nefrologia), Onco-Hematology e Immunology.

Lauree Specialistiche

♦︎ Oncologia
♦︎ Ematologia
♦︎ Cardiologia
♦︎ Immunologia
♦︎ Neurologia
♦︎ Dermatologia

* Nella Motivation Letter specificare l'area terapeutica di proprio interesse tra: Chronic Disease (cardiologia, malattie infiammatorie, osteoporosi, nefrologia), Onco-Hematology e Immunology.

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

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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.

JOB REQUIREMENTS

• Bachelor's degree in Medicine
• Specialization in internistic disciplines or pharmacology preferred
• Fluent English in written and verbal format
• Optimal use of Microsoft Office (PowerPoint, Excel and Word)
• Communication and public speaking skills
• Relational and organizational skills
• Team working skills
• Up to 30% overnight travel, including abroad required.

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

 

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CHI SIAMO

Bristol Myers Squibb è un'azienda biofarmaceutica globale la cui missione è quella di scoprire, sviluppare e rendere disponibili farmaci innovativi dedicati a pazienti che combattono contro gravi malattie. Siamo ispirati da una sola visione: trasformare la vita dei pazienti attraverso la scienza. Puntiamo all’eccellenza scientifica, investendo in ricerca e sviluppo per rendere disponibili farmaci innovativi ad elevato standard qualitativo che rispondano ai bisogni clinici non soddisfatti.

Con una pipeline tra le più ampie e diversificate del settore farmaceutico, siamo all’avanguardia nello sviluppo di terapie innovative che migliorino la sopravvivenza e la qualità di vita dei pazienti.

All’interno della nostra Direzione Medica lavorano Medici con il ruolo di Medical Science Liaison che svolgono un ruolo fondamentale nel trasferire le nostre conoscenze scientifiche per avere un impatto positivo sul cambiamento della vita dei pazienti.

Il Medical Science Liaison è il primo punto di contatto per qualsiasi aspetto o problema medico/scientifico relativo ai prodotti assegnati, impegnato nello Scambio Scientifico sia con i team di Bristol Myers Squibb, sia con i principali esperti esterni, gli operatori sanitari e gli sperimentatori clinici.

Il Medical Science Liaison si confronta con esperti a livello nazionale ed internazionale per aumentare l’attenzione sulla malattia e sulle opzioni terapeutiche, per identificare bisogni clinici insoddisfatti, lacune nelle evidenze scientifiche e per ottenere insights.

IL MEDICAL SCIENCE LIAISON IN BMS è responsabile di:

• Fungere da punto di contatto all'interno del team Medical Affairs per gli Opinion leaders e gli esperti nella tua area geografica al fine di soddisfare le loro esigenze di approfondimento scientifico nell'area terapeutica e per i prodotti assegnati, garantendone l'uso sicuro, efficace e appropriato.

• Assicurare la leadership scientifica costruendo relazioni professionali con gli Opinion leaders e gli esperti delle aree terapeutiche.

• Garantire una forte presenza medico-scientifica nei principali centri accademici, facilitando le iniziative di ricerca e di formazione e supportando le richieste di approfondimento scientifico sulle aree terapeutiche assegnate.

• Assistere nell'avvio, supervisione e follow-up degli studi clinici e dei progetti medici avviati nell'ambito dell'area terapeutica e del territorio assegnato.

• Fungere da punto di contatto con gli Opinion leaders per facilitare la condivisione di idee di ricerca clinica o pre-clinica e la sottomissione di richieste di supporto per la ricerca sponsorizzata dagli sperimentatori (Investigator Sponsored Research, ISR) al team medica locale e/o a quello Worldwide, a seconda dei casi.

• Interagire con gli Opinion leaders che l'azienda desidera coinvolgere in attività come potenziali collaborazioni di ricerca, ruoli educazionali o di consulenza (Advisory Boards, Congressi, Simposi, ecc.), garantendo al contempo un elevato livello di integrità scientifica ed educazionale.

• Partecipare a congressi scientifici di rilievo. Collaborare con gli stakeholder interni per sviluppare una reportistica tempestiva sui dati chiave e altre informazioni scientificamente rilevanti per informare le iniziative strategiche di BMS.

Altre attività:

• Fornire supporto scientifico alla preparazione della Field Force per garantire standard di alta qualità nello svolgimento delle loro attività.

• Supportare i medici responsabili di prodotto e il dipartimento di Farmacovigilanza nella gestione degli eventi avversi (ad es. raccolta di informazioni di follow-up).

• Supporto al team WW per le attività assegnate.

Se hai voglia di nuovo sfide, vuoi continuamente imparare e migliorarti, ti piace un lavoro dinamico e credi nel gioco di squadra, allora questo è il lavoro che fa per te.

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

 

 

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Reports into: Senior Director, TA Head Non-obstructive Respiratory Diseases, Global Clinical Development AIR

Department: Global Research & Development

Location: Europe / Remote

Opportunity to join a dynamic and dedicated Global Clinical Development team committed to advancing therapies for patients across a broad spectrum of respiratory diseases.

About us:
Headquartered in Parma, Italy, Chiesi Group is an international research-focused pharmaceuticals and healthcare group with 90 years of experience, operating in over 30 countries with more than 7,000 employees. We are proud to be the largest global pharmaceutical group to be awarded B-Corp Certification, a recognition of high social and environmental standards. 

Role Description:
The Clinical Research Physician (CRP) plays a key role in the medical oversight of Phase 1 to 3 clinical trials within our Respiratory Unit in Global Clinical Development. The CRP ensures scientific and medical integrity in the development and execution of clinical studies, contributing to the overall global clinical strategy and regulatory submissions.

CRP are able to work well in a matrix environment and is an integral member of the cross-functional clinical study team, using therapeutic expertise to ensure the incorporation of robust scientific principles into study design and conduct and to enhance competencies across R&D.

Main Responsibilities:

• Provide medical and scientific input into clinical trial design and execution in accordance with the Clinical Development Plan and related key clinical documentation (e.g. clinical section of the Investigator’s Brochure, Protocols and Clinical Study Reports).
• Conduct ongoing medical and scientific review of clinical trial data, ensuring data integrity, patient safety and the ongoing benefit-risk assessment.
• Be responsible for the clinical interpretation of study data and communication to internal and external stakeholders.
• Collaborate with Clinical Program Leaders, statisticians, regulatory affairs, and other key functions to drive clinical development plans and contributes to regulatory submission documentation.
• Engage with external experts, regulatory bodies, ethics committees, investigators, and safety monitoring committees to ensure alignment with scientific and medical needs.
• Ensure the safeguard of Patients Safety: in collaboration with and in support of Corporate Pharmacovigilance identify safety signals, review narratives, take actions with investigators when Serious/unexpected Adverse Events are reported.

Experience Required:
At least 3 years in the pharmaceutical industry preferred although equivalent expertise in clinical or academic research will be considered, preferably within the Respiratory or Immunology therapeutic areas.

Education:
Medical Doctor Degree from a recognised institution; certification in Respiratory or Immunology considered an advantage.

Languages:
Fluency in spoken and written English.

Technical Skills:

• Excellent writing skills in order to effectively contribute to study documentation and reports.
• Outstanding communication skills with ability to interact with all internal stakeholders and external academic and regulatory experts.
• Strong understanding of GCP, regulatory requirements, and clinical trial methodologies.
• Ability to interpret and effectively communicate complex clinical and scientific data, and literature. 

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Obiettivo del ruolo:

Essere il partner scientifico di riferimento per stakeholder interni ed esterni, supportando le strategie aziendali attraverso la comunicazione scientifica e la collaborazione cross-funzionale.

Responsabilità principali:

Generazione di evidenze: supporto a studi locali (ISS, NIS), identificazione di gap scientifici.

Educazione medica: diffusione della scienza tramite eventi e interazioni dirette con HCP/KOL.

Engagement con KOL: mantenimento di relazioni strutturate con esperti e società scientifiche.

Pianificazione pubblicazioni: supporto a pubblicazioni locali e narrative review.

Guida medica: formazione interna e supporto scientifico per decisioni strategiche.

Requisiti:

Laurea scientifica (es. Biologia).

Esperienza consolidata in Medical Affairs e/o ambito clinico CV.

Conoscenza delle normative locali per eventi scientifici.

Competenze chiave:

Comunicazione efficace e ascolto attivo.

Collaborazione cross-funzionale e partnership.

Comprensione scientifica e clinica.

Competenze digitali e organizzative.

 

 

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

 

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Reports into: Therapeutic Area Head – Respiratory Unit, Global Clinical Development

Department: Global R&D

Location: Europe / Remote

Opportunity to join a dynamic and dedicated Global Clinical Development team committed to advancing therapies for patients across a broad spectrum of respiratory diseases.

About us:
Headquartered in Parma, Italy, Chiesi Group is an international research-focused pharmaceuticals and healthcare group with over 85 years of experience, operating in over 30 countries with more than 7,000 employees. We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social and environmental standards. 

Role Description:
The Clinical Research Physician (CRP) plays a key role in the medical oversight of Phase 1 to 3 clinical trials in Respiratory within Global Clinical Development. They ensure scientific and
medical integrity in the development and execution of clinical studies, contributing to the overall clinical strategy and regulatory submissions.

They are able to work comfortably in a matrix environment and is an integral member of the cross-functional clinical study team. They use therapeutic expertise to ensure incorporation of robust scientific principles into study design and conduct and to enhance competencies across R&D.

Main Responsibilities:

• Provide medical and scientific input into clinical trial design and execution in accordance with the Clinical Development Plan and related key clinical documentation (e.g. clinical section of the Investigator’s Brochure, Protocols and Clinical Study Reports).
• Conduct ongoing medical and scientific review of clinical trial data, ensuring data integrity, patient safety and the ongoing benefit-risk assessment.
• Be responsible for the clinical interpretation of study data and communication to internal and external stakeholders.
• Collaborate with Clinical Program Leaders, statisticians, regulatory affairs, and other key functions to drive clinical development plans and contributes to regulatory submission documentation.
• Engage with external experts, regulatory bodies, ethics committees, investigators, and safety monitoring committees to ensure alignment with scientific and medical needs.

Experience Required:
At least 3 years in the pharmaceutical industry preferred although equivalent expertise in clinical or academic research will be considered, preferably within the Respiratory or Allergy & Immunology therapeutic areas.

Education: 
Medical Doctor Degree from a recognised institution; certification in Pulmonary or Allergy & Immunology considered an advantage.

Languages:
Fluency in spoken and written English.

Technical Skills:

• Excellent writing skills in order to effectively contribute to study documentation and reports.
• Outstanding communication skills with ability to interact with all internal stakeholders and external academic and regulatory experts.
• Strong understanding of GCP, regulatory requirements, and clinical trial methodologies.
• Ability to interpret and effectively communicate complex clinical and scientific data, and literature.

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Career Category: Medical Affairs
Role: MEDICAL SCIENCE LIAISON IMMUNOLOGY | NORD

HOW MIGHT YOU DEFY IMAGINATION?

You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.

LIVE. What you will do

Let’s do this. Let’s change the world. In this vital role you will:

• Be field-based medical expert in the Medical Science Liaison (MSL) group within Medical organization;
• Be an integral position in communicating accurate, clear, and valued information regarding our science and products to multiple levels within the medical community and are responsible for gathering field insights for  internal stakeholders;
• Support medical strategic roles in developing local territory R&D tactics;
• Engage with healthcare stakeholders to educate and communicate clinical and scientific data to advance the scientific platform as aligned with Amgen’s corporate goals and objectives;
• Educate and communicate clinical value, outcomes, and economic data to payers, providers, key stakeholders, advocacy, and access enablers;
• Respond to unsolicited inquiries consistent with the MSL compliance standards;
• Provide and/or present field observations and insights to internal stakeholders;
• Execute scientific engagement plan according to annual MSL goals and metrics;
• Develop and implement local OL plans in line with scientific engagement plan;
• Support speaker training as requested and ensure the speakers are updated on new data;
• Support Amgen sponsored research and may serve as a study lead;
• Liaise with potential investigators in non-sponsored clinical research;
• Lead and/or participate on project teams that support MSL strategies and tactics as delegated by MSL leadership;
• Advance MSL value proposition, identify gaps, achieve results, and set an example for others to follow by consistently demonstrating Amgen values and leadership attributes. Demonstrate tact and professionalism when communicating and interacting with others;
• Lead and support congress activities as aligned with strategy;
• Compliantly collaborate with cross-functional colleagues;
• Maintain clinical acumen and expertise and timely completion of assigned training. May serve as a training lead;
• Cultivate long term relationships.

Outputs

• Documentation of MSL quantitative (CRM system) and qualitative accomplishments;
• Provision and/or presentation of field insights;
• OL profiles, plans, and reports;
• Site identification/profiling and recommendations (if study lead, produce reports and communication updates);
• Educational program and congress key learnings;
• May generate and present field observations and insights;
• May assist with dashboard report development.

WIN. What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The resource we seek is a person with these qualifications.

• Doctoral Degree or Master’s degree in Sciences or Medicine;
• Five years of industry experience in Scientific/Medical Affairs at a biotech or pharmaceutical company (of which at least two years in a Medical Science Liaison role), or five or more years focused on clinical practice, clinical research, or medical research. Experience in a medically-related field can include post-doctoral training (i.e., residencies and/or fellowships);
• Scientific expertise in rare diseases or immunology or endocrinology areas is a plus;
• Strong project management and presentation skills;
• Good knowledge of clinical research, drug safety, legal and compliance environment;
• Willingness to continuously expand medical, scientific, market, and industry knowledge.
• Science Based attitude, data driven, outside-in thinking and strategic overview;
• Result-driven and set to achieve goals;
• Patient centric and influential;
• Fluency in written and spoken English;
• Based in the North of Italy.

THRIVE. What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

• Full support and resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act.

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

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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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As a Medical Advisor at Novartis, you will play a strategic role in shaping the medical positioning of both marketed and pipeline compounds within your assigned therapeutic area. You will act as a key scientific expert, providing up-to-date medical insights and driving Novartis’ scientific messaging to both internal and external stakeholders. In close collaboration with Country, Regional, and Global teams, you will co-design the clinical development, launch strategy, and lifecycle management of assigned products. You will contribute to the implementation of local and global therapeutic area strategies through innovative and integrated evidence generation. Additionally, you will be responsible for the planning and execution of medical projects and events, ensuring alignment with medical strategic objectives and always placing the needs of patients and those who care for them at the center of your work.

Key responsibilities:

Your responsibilities include, but are not limited to:

• Strategic Support for Drug Development and Lifecycle Management: provide strategic medical input to the development, registration, launch, and lifecycle management of assigned pipeline and marketed compounds, ensuring alignment with both local and global therapeutic area strategies.
• Scientific Guidance Across Internal Functions: act as a medical and scientific expert by supporting various internal stakeholders—including regulatory, market access, marketing, and clinical teams—ensuring consistent and high-quality scientific communication.
• Cross-functional and Cross-regional Collaboration: collaborate effectively with local, regional, and global Medical Affairs, Global Drug Development (GDD), Patient Advocacy, and Public Affairs teams to drive aligned and impactful execution of medical plans and initiatives.
• Clinical Studies and Scientific Publications: contribute to the planning, execution, and oversight of global, regional, and local clinical studies. Support timely and compliant scientific dissemination through publications, adhering to GCP, ICH, and local regulations.
• Evidence Generation and Real World Data Initiatives: identify Real World Evidence (RWE) needs and lead the implementation of innovative evidence-generation approaches to bridge knowledge gaps, support patient access, and improve clinical outcomes.
• Scientific Training and Educational Leadership: develop and deliver tailored scientific training and disease/product education for internal teams (e.g., field force, MSLs) and external partners, ensuring accurate and up-to-date communication of clinical data.
• Medical Governance, Ethics, and Compliance: ensure that all medical activities comply with ethical standards, corporate policies, and local regulations—including oversight of safety reporting, GCP adherence, and review of promotional and non-promotional materials.
• Medical Projects and Budget Oversight: lead or contribute to the planning and execution of non-promotional medical initiatives and scientific events. Manage assigned Medical Affairs budgets efficiently, and when required, lead cross-functional medical project teams.

Essential Requirements

• MD Degree
• English and Italian: Proficient
• Good planning skills
• Good negotiation skills
• Medical and scientific writing skills
• Good communication skills
• Team player in a matrix organization.

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

 

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Obiettivo del ruolo:

Facilitare l’esecuzione di studi clinici nelle nuove aree terapeutiche fornendo competenze medico-scientifiche e coordinando processi cross-funzionali.

Responsabilità principali:

Identificazione KOL e centri di ricerca: mappatura e coinvolgimento di esperti, centri e associazioni pazienti.

Raccolta di insight scientifici: interazione con esperti per ottimizzare la fattibilità e l’esecuzione degli studi.

Supporto alle attività cliniche: contributo alla selezione dei siti, formazione, visite, e comunicazione dei risultati.

Guida medica: formazione interna, supporto scientifico a team cross-funzionali e stakeholder esterni.

Requisiti:

Laurea in Medicina, PhD, Farmacia o Scienze con forte background clinico.

≥3 anni di esperienza in ricerca clinica o industria farmaceutica.

Esperienza come investigatore clinico preferita.

Conoscenza del sistema sanitario locale e dello sviluppo farmaceutico.

Competenze chiave:

Comunicazione scientifica e presentazioni efficaci.

Leadership personale e gestione stakeholder.

Conoscenza terapeutica e capacità di influenzare.

Orientamento ai risultati e comprensione del business.

 

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

 

 

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! Questa posizione funziona come candidatura spontanea aperta a tutte le specializzazioni in Medicina.

Job Description

✦ Location: Rome, Metropolitan City of Rome
✦ Full-time
✦ Travel: Yes, 50% of the time

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