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Head Office: 
- Palermo 
- Reggio Calabria
- Catania
- Messina

Travel: Yes, 50 % of the Time

Job Type: Experienced

Schedule: Full-time

MAIN ACTIVITIES AND RESPONSIBILITIES

• Provide scientific and technical leadership to ensure professional and credible relationships with thought leaders and external experts of strategic importance to AbbVie. Ensure a strong medical and scientific presence for AbbVie in key academic centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest to AbbVie.
• Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations. Work collaboratively and cross-functionally with other in-field members while retaining functional independence.
• Assist in the initiation, oversight and follow up of assigned clinical studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e.g. pre and post marketing clinical activities such as registry/database projects, epidemiological surveys, post-authorization studies (phase IV) and Phase II-III trials. All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and AbbVie R&D (GPRD) SOPs.
• Act as the point of contact with thought leaders to facilitate investigator initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate
• Serve as a point of contact within the Medical Affairs team for thought leaders and external experts within an assigned geographic area in order to satisfy their needs for scientific knowledge in a therapeutic area and, when requested, relevant AbbVie medicines, to support their safe, effective and appropriate use.
• Deliver credible presentations on scientific matters to physicians, individually or in groups (meetings, clinical sessions, etc.), where requested, but with the focus on Tier 1, 2 and 3 thought leaders.
• Participate in the selection process to identify appropriately qualified thought leaders the Company would wish to engage in collaborative efforts – such as potential research collaborations, or educational and advisory roles (Advisory Boards, Congresses, Symposia, etc.); while ensuring a high level of scientific or educational integrity in these collaborative efforts.
• Identify, collect and internally provide insights into medical and scientific field intelligence – for example, competitor research and medical strategies, educational activities. Attend relevant scientific meetings and Conferences. Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform AbbVie strategic priorities and initiatives.
• Upon request, assist physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements. Provide key thought leaders / external experts and internal medical and clinical teams with scientific and technical support for publications of scientific or medical interest.
• Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.
  
  

 JOB REQUIREMENTS

• Advanced degree (e.g. PharmD., MD, PhD) in a relevant scientific discipline is preferred (most preferred: Gastroenterology; but also Internal Medicine is appreciated) but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered.
• Experience in developing and maintaining expert knowledge for the assigned therapeutic area, and in medical research in general.
• Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.
• Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research
• Ability to comprehensively learn about new subject areas and environments.
• Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians and other healthcare decision makers.
• A good understanding of written and oral English is desirable.
• High customer orientation.
• Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.

 

AbbVie is an equal opportunity employer including disability/vets. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a disabled veteran, recently separated veteran, Armed Forces service medal veteran or active duty wartime or campaign badge veteran or a person’s relationship or association with a protected veteran, including spouses and other family members, or any other protected group status. We will take affirmative action to employ and advance in employment qualified minorities, women, individuals with a disability, disabled veterans, recently separated veterans, Armed Forces service medal veterans or active-duty wartime or campaign badge veterans. The Affirmative Action Plan is available for viewing in the Human Resources office during regular business hours.

 

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Array ( [id] => 1007 [azienda_id] => 199 [lauree] => {null} [settore] => [ruolo] => [inserimento] => [time_c] => 0 [last_mod] => 1683182486 [title] => Medical Science Liaison (MSL) Immunology & Fibrosis SUD Italia [body] =>

Descrizione posizione lavorativa
In Bristol Myers Squibb, siamo ispirati da un'unica visione: trasformare la vita dei pazienti attraverso la scienza. In oncologia, ematologia, immunologia e malattie cardiovascolari - una delle pipeline più diversificate e promettenti del settore - ciascuno dei nostri colleghi contribuisce con passione alle innovazioni che guidano un cambiamento significativo. Diamo un tocco umano a ogni trattamento di cui siamo pionieri. Unisciti a noi e fai la differenza.

Hai voglia di nuovo sfide? Vuoi continuamente imparare e migliorarti? Ti piace un lavoro dinamico e credi nel gioco di squadra? Se hai risposto sì a queste 3 domande continua a leggere perché questo è il lavoro che fa per te.

In qualità di Medical Science Liaison (MSL) Immunology & Fibrosis SUD Italia svolgerai un ruolo fondamentale nel trasferire le nostre conoscenze scientifiche per avere un impatto positivo sul cambiamento della vita dei pazienti.

Sarai il primo punto di contatto per qualsiasi aspetto o problema medico/scientifico relativo ai prodotti a te assegnati, impegnandoti nello Scambio Scientifico sia con i team di Bristol Myers Squibb, sia con i principali esperti esterni, gli operatori sanitari e gli sperimentatori clinici.

Ti confronterai 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.

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.

IL MEDICAL SCIENCE LIAISON IN BMS

In qualità di Medical Science Liaison (MSL) Immunologia sarai 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.

REQUISITI ESSENZIALI

• Laurea in medicina e chirurgia
• Buone capacità di comunicazione scritta e orale
• Buona comprensione dell'inglese scritto e orale
• Ottime capacità sociali
• Adeguate competenze informatiche (Office, Outlook, Web, ecc.)
• Inclinazione al lavoro di squadra
• Capacità di lavorare in modo indipendente e di assegnare priorità alle diverse attività
• Patente di guida
• Domicilio: Sud Italia
• Disponibilità a viaggiare fino al 70% del tempo di lavoro

REQUISITI AUSPICABILI

• Doti di presentazione di dati scientifici
• Conoscenza dell'area terapeutica Immunologia
• Esperienza nella preparazione ed esecuzione del lancio di un prodotto
• Conoscenza dei requisiti normativi locali relativi alle attività del Medical Affairs

 

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Descrizione posizione lavorativa
In Bristol Myers Squibb, siamo ispirati da un'unica visione: trasformare la vita dei pazienti attraverso la scienza. In oncologia, ematologia, immunologia e malattie cardiovascolari - una delle pipeline più diversificate e promettenti del settore - ciascuno dei nostri colleghi contribuisce con passione alle innovazioni che guidano un cambiamento significativo. Diamo un tocco umano a ogni trattamento di cui siamo pionieri. Unisciti a noi e fai la differenza.

IL MEDICAL SCIENCE LIAISON IN BMS

In qualità di Medical Science Liaison (MSL) Cardiovascular sarai 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.

REQUISITI ESSENZIALI

• Laurea in Medicina e Chirurgia
• Buone capacità di comunicazione scritta e orale
• Buona comprensione dell'inglese scritto e orale
• Ottime capacità sociali
• Adeguate competenze informatiche (Office, Outlook, Web, ecc.)
• Inclinazione al lavoro di squadra
• Capacità di lavorare in modo indipendente e di assegnare priorità alle diverse attività
• Patente di guida
• Domicilio: Lazio (preferibilmente), Campania
• Disponibilità a viaggiare fino al 70% del tempo di lavoro

REQUISITI AUSPICABILI

• Doti di presentazione di dati scientifici
• Conoscenza dell'area terapeutica Cardiovascolare
• Esperienza nella preparazione ed esecuzione del lancio di un prodotto
• Conoscenza dei requisiti normativi locali relativi alle attività del Medical Affairs

Sede: Field-based

Area di lavoro: Lazio, Campania, Molise, Basilicata, Puglia, Calabria

 

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POSITION: Medical Manager 

REPORTS TO: Medical Affairs Director

BASED: Florence

EXPECTED TRAVEL: 30%

 

CONTEXT

The Medical Affair Team has the primary goal to support scientific information and development of the Menarini products. The Medical Manager works closely with the Product Manager. Other internal relationships include relations with MSL Lead, Pharmacovigilance and Regulatory Affairs team, Medical Reps. External relationships include scientific society and KOLs.

MAIN ACTIVITIES AND RESPONSIBILITIES

• Cooperate with Product Manager in developing 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;
• 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 internal medicine or pharmacology are preferred
• Fluent English written and spoken
• Optimal use of Microsoft Office (PowerPoint, Excel and Word).
• Excellent communication and public speaking skills.
• Excellent organizational skills

 

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Array ( [id] => 1012 [azienda_id] => 158 [lauree] => {null} [settore] => [ruolo] => [inserimento] => [time_c] => 0 [last_mod] => 1683622833 [title] => Chiesi - candidatura spontanea per studenti/laureati in Medicina e specializzazioni [body] =>

Gentile studente/ssa,
Devi sapere che Chiesi è spesso alla ricerca di medici da inserire ed accogliere in azienda.
Chiesi, per il suo dinamismo e il forte orientamento alla ricerca e all’innovazione, è un’azienda ricca di opportunità non tradizionali quanto interessanti da proporre ad un profilo medico.
Se ti interessa essere protagonista all’interno di un’azienda fortemente orientata alla ricerca e allo sviluppo, contribuendo allo sviluppo di soluzioni terapeutiche innovative che migliorino la qualità della vita delle persone, Chiesi è il posto che fa per te!
Nel caso in cui fossi interessat* ad una esperienza professionale presso la nostra azienda, saremmo felici di ricevere una tua candidatura.
Per candidarti ti basterà cliccare sul bottone APPLY qui sotto oppure partecipare alla diretta di martedì 16 maggio ore 15 e inquadrare il QR Code a fine presentazione e provvedere al caricamento del tuo curriculum.

Sperando di sentirti presto,
ti auguriamo una buona continuazione,
Talent Acquisition Team

 

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Head Office: Rome

Travel: No

Job Type: Experienced - Medical Advisor for Gastroenterology Area

Schedule: Full-time

MAIN ACTIVITIES AND RESPONSIBILITIES

• In cooperation with affiliate / Area Medical teams, Marketing, RA, Clinical and other functional areas, provides leadership, oversight and support for assigned products/projects.
• Establishes and approves scientific methods for hypotheses, rational, design of affiliate/Area/Global protocols and their reports.
• Participation in design and execution of clinical trial safety, product safety and risk management plans. May also carry responsibility for routine and ad hoc safety monitoring reports to regulatory agencies. May review, assess and report applicable Adverse Events (AE’s) and Serious Adverse Events (SAE’s) if assigned to AbbVie conduct on clinical studies.
• Oversees the conduct of clinical trials and is medically and scientifically accountable for resolution of safety (AE’s & SAE’s) issues, interpretation of statistical analyses for clinical significance, PI selection, scientific documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities. NB: All clinical research / development activities for products under development, and for post approval commitments such as regulatory agency mandated trials,
• or those intended to support product registration or to generate data for label inclusion remain the primary responsibility of TA development teams. Initiates medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy.
• Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information. Keeps a breast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource.
• Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as the scientific team interface for key regulatory discussions
• May act as medical/scientific leader for projects within an area or across several areaAssists with the scientific review, development, approval, execution and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
• May lead cross functional sub teams responsible for discrete projects within the therapeutic area (individual publications or study collaborations)
• Initiate research projects and drive them to completion, resulting in high quality publications. Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities

 JOB REQUIREMENTS

• Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D. meet requirements) with relevant therapeutic specialty in an academic or hospital environment. Completion of residency and/or fellowship is preferred.
• Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred. Proven leadership skills in a cross-functional global team environment. Ability to interact externally and internally to support global business strategy. Ability to run a clinical study or medical affairs team independently with little supervision.
• Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
• Expert knowledge in a relevant therapeutic specialty.
• Ability to interact externally and internally to support global business strategy. Must possess excellent oral and written English communication skills.
• For clusters of countries multi-lingual skills of language is preferred.

 

AbbVie is an equal opportunity employer including disability/vets. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a disabled veteran, recently separated veteran, Armed Forces service medal veteran or active duty wartime or campaign badge veteran or a person’s relationship or association with a protected veteran, including spouses and other family members, or any other protected group status. We will take affirmative action to employ and advance in employment qualified minorities, women, individuals with a disability, disabled veterans, recently separated veterans, Armed Forces service medal veterans or active-duty wartime or campaign badge veterans. The Affirmative Action Plan is available for viewing in the Human Resources office during regular business hours.

 

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Purpose
Contribute to the production of the Common Technical Document, in terms of validation of scientific documents relevant to the concerned clinical studies (e.g., study protocol, CRF, Investigator Brochure, clinical study report), also representing the Company in front of the institutional authorities concerned.

Support the relevant clinical studies within the concerned development program for the medical/scientific aspects, especially those requiring his/her Therapy Area expertise, where she is deeply committed to act as the main reference point.

Develop and enhance experience in management of clinical studies, working in collaboration with the Clinical Program Leader and the other involved jobs, as well as in the implementation of specific clinical study designs within the concerned development program

Main responsibilities

• Acting as a member of Extended Clinical Team and/or Clinical Study Team, in cooperation with other Study Team Members, deliver results of the assigned Clinical Studies and related Key Clinical Documents, in accordance with the Clinical Development Plan and the related agreed timelines (e.g., clinical section of the investigator’s Brochure, clinical section of the Investigational Medical Product Dossier, assigned Protocols, Protocol amendments & Clinical Study Reports, etc).
• Assigned to each protocol sponsored by Chiesi and can be assigned by the CPL to provide the clinical input to functional portions of the CDP (outlines design, cooperation to the timely and quality execution of the plan through interaction with Study Team Members).
• Starting from her Therapy Area expertise, aim at meeting the needs of internal and external customers, acting as Subject Matter Expert in the assigned product(s) and relevant disease(s) area, maintaining and enhancing knowledge in relevant therapeutic or technical areas and in global regulations/guidelines, identifying potential trends and assisting in internal decision making, securing timely publication of all clinical data produced according to the agreed publication plan.
• Ensure application of enhanced, up to date trial designs by partnering with all relevant disciplines, as well as of Company standards, SOPs and achievement of agreed KPIs.
• Cooperate in the design of post-registration clinical studies to secure growth of the brand into the marketplace in line with the Lifecycle Management Plan and the relative Clinical Development Plan.
• Represent the Company in front of Institutional Authorities (acting as the medical point of contact for Clinical Operations on clinical content of assigned protocols for investigators’ meeting, responding to EC inquiries, representing Chiesi Clinical Expertise in public sessions of Data Safety Monitoring Board Meetings, taking decision to amend protocol when acting on behalf of the CPL).
• Responsible for interpretation of clinical data, attend blind review meeting as support of study manager, and, when delegated by the CPL, get inside the data, understands and interrogate it, work with the statistician for definition of SAP and definition of additional data sets/data mining, consult CPL and Head of GCD to discuss emerging data.
• 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, ensure a full understanding of key Adverse Events and Serious Adverse Events and appropriate actions.
• Ensure the on-going risk benefit assessment, caring the safety and efficacy signal detection/response during conduct of assigned studies, dealing with alerts emerging during conduct of assigned studies, providing the interim understanding of data.
• Act as medical writer when required and in general act in compliance with ICH/GCP, SOPs and Regulatory Guidelines.
• Accountable for the delivery of high-quality scientific and clinical assessment of new product opportunities for in-licensing, including the hypothesis for the clinical development plan (including standardized costs) and life-cycle management, and the clinical/ development risks

Educational Qualifications

• Medical Doctor Degree
• medical skills in her specific area

Professional experience
Preferred pharmaceutical industry: Respiratory, Pneuomology, Internal medicine or Immunology.

Languages
Native Italian
Intermediate English

Technical Skills
Microsoft office package

Soft Skills

• Problem solving
• Interpersonal Skills
• Teamworking
• Time Management

 

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