Lavori attuali relativi a Clinical Research Associate - Bagni Di Tivol - Novo Nordisk Pharma

  • Senior Clinical Research Associate

    5 giorni fa

    Bagni Di Tivol, Italia Merck Sharp & Dohme (MSD) A tempo pieno

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Merck Sharp & Dohme (MSD). As a Clinical Research Associate, you will be responsible for ensuring the smooth conduct of clinical trials at assigned sites, ensuring compliance with regulatory requirements, and providing high-quality support to investigators and site...

  • Clinical Research Associate

    2 settimane fa

    Bagni Di Tivol, Italia Merck Sharp & Dohme (MSD) A tempo pieno

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Merck Sharp & Dohme (MSD). As a key member of our site management team, you will be responsible for ensuring the successful execution of clinical trials at assigned sites.Key ResponsibilitiesDevelop and maintain strong relationships with site investigators and staff to...

  • Senior Clinical Research Associate

    4 mesi fa

    Bagni Di Tivol, Italia Merck Sharp & Dohme (MSD) A tempo pieno

    Job DescriptionWe aspire to be the premier research-intensive biopharmaceutical company in the world.We demonstrate our commitment to patients and population health by increasing access to health care through far-reaching policies, programs and partnerships. Today, we continue to be at the forefront of research to prevent and treat diseases that threaten...

  • Clinical Operations Manager Lead

    2 mesi fa

    Bagni Di Tivol, Italia Merck Sharp & Dohme (MSD) A tempo pieno

    Job DescriptionThis role is accountable for the execution and oversight of local operational clinical trial activities in compliance with ICH/GCP and country regulations, our Company policies and procedures and with quality standards, both internally and externally.The person has ownership, oversight, and impact on local financial compliance and on...

  • Pharmacy Investigational Product Specialist

    5 giorni fa

    Bagni Di Tivol, Italia IQVIA A tempo pieno

    Job Title: Pharmacy Investigational Product SpecialistAt IQVIA, we are seeking a highly skilled Pharmacy Investigational Product Specialist to join our team. As a key member of our Sponsor Dedicated (cFSP) team, you will play a critical role in driving healthcare forward by ensuring the safe, efficient, and effective preparation of investigational products...

  • Pharmacy Investigational Product Specialist

    5 giorni fa

    Bagni Di Tivol, Italia IQVIA A tempo pieno

    Job Title: Pharmacy Investigational Product SpecialistAt IQVIA, we are seeking a highly skilled Pharmacy Investigational Product Specialist to join our team. As a key member of our Sponsor Dedicated (cFSP) team, you will play a critical role in driving healthcare forward by ensuring the safe, efficient, and effective preparation of investigational products...

  • Post-market Clinical Follow-up

    1 mese fa

    Provincia di Roma, Lazio, Italia ClinChoice A tempo pieno

    Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. **ClinChoice is searching for a Post-Market Clinical Follow-up (PMCF) Medical Writer Consultant for 1 year contract, **to join one of our...

  • Clinical Application Specialist HRm

    4 mesi fa

    Casalnuovo di Napoli, Italia Philips A tempo pieno

    **Job Title**: Clinical Application Specialist HRM (South Italy) **Clinical Application Specialist**: Driving clinical decision support for products and solutions including sales presentations, product demonstrations, and educating sales teams on emerging clinical issues for HRM (Heart Rythm Management) segment. **Your role**: - Providing primary training...

  • Office Assistant for Logistics and Clinical Affairs

    4 mesi fa

    Provincia di Terni, Umbria, Italia Meditrial Europe Ltd. A tempo pieno

    Meditrial is a full-service digital research organization with a foundation in clinical trial research, education, regulatory and market access. Meditrial has been leading the medical tech industry by delivering unparalleled outcomes for innovators. Our successful track record supporting medical device and biotechnology companies in all phases of clinical...

  • Associate Director, Statistics

    4 mesi fa

    Provincia di Cuneo, Piemonte, Italia PHASTAR A tempo pieno

    Overview: **About Phastar** Phastar brings data to life! We are an award-winning specialist biometrics contract research organization (CRO) that works with pharmaceutical, biotechnology and medical device companies to provide statistical consulting, analysis and reporting, data management, and data science services. Our unique approach to data analysis,...

  • Regulatory Affairs Specialist Md

    3 mesi fa

    Tavarnelle Val di Pesa, Italia GIGROUP A tempo pieno

    Marketing, Clinical Research, Regulatory e Operation dei settori Farmaceutico e Medicale e per le mansioni legate all’assistenza al cliente del mondo distributivo con impatto sulla salute. Il nostro cliente è Endostart Srl, start-up medtech innovativa nel settore dei dispositivi medici, impegnata nello sviluppo, produzione e commercializzazione di...

  • Scientific Project Manager

    3 mesi fa

    Cavenago di Brianza, Italia Openjobmetis S.p.A. A tempo pieno

    Openjobmetis spa Divisione Permanent ricerca e seleziona per assunzione diretta presso importante azienda del settore chimico di Cavenago **Posizione**: **Scientific Project Manager - Accountable for coordination of the operational management of assigned projects in order to develop the scientific programs in line with Company goals. - Creates, optimizes,...

  • Project Manager

    2 settimane fa

    Provincia di Roma, Lazio, Italia ClinChoice A tempo pieno

    Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. **ClinChoice is searching for a Project Manager - R&D (Life Sciences) Consultant for 12 months Contract with possibility of extension **to join one of...

  • Customer Service Specialist

    4 mesi fa

    Castelnovo di Sotto, Italia Eurofins Italy A tempo pieno

    **Descrizione dell'azienda**: - Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins...

  • Farmacista Specializzato

    2 settimane fa

    San Donà di Piave, Veneto, Italia Gi Group S.p.A A tempo pieno

    Gi Group S.p.A. è una multinazionale del lavoro italiana che offre opportunità di carriera ai candidati in ambito Sales & Marketing, Clinical Research, Regulatory e Operation dei settori Farmaceutico e Medicale.Siamo un team di professionisti appassionati che lavoriamo per accompagnare i nostri candidati verso le mansioni ed i contesti aziendali più...

  • Farmacista Specializzato

    2 settimane fa

    San Donà di Piave, Veneto, Italia Gi Group S.p.A A tempo pieno

    Gi Group S.p.A. è una multinazionale del lavoro italiana che offre opportunità di carriera ai candidati in ambito Sales & Marketing, Clinical Research, Regulatory e Operation dei settori Farmaceutico e Medicale.Siamo un team di professionisti appassionati che lavoriamo per accompagnare i nostri candidati verso le mansioni ed i contesti aziendali più...

  • Statistical Programmer Iii

    3 settimane fa

    Provincia di Cuneo, Piemonte, Italia PHASTAR A tempo pieno

    Overview: **THE COMPANY** Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality...

  • Statistical Programmer Ii/iii

    3 mesi fa

    Provincia di Cuneo, Piemonte, Italia PHASTAR A tempo pieno

    Overview: THE COMPANY Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics,...

  • Principal Statistical Programmer

    3 giorni fa

    Provincia di Cuneo, Piemonte, Italia PHASTAR A tempo pieno

    Overview: **THE COMPANY** Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality...

  • Field Application

    3 settimane fa

    Casalnuovo di Napoli, Italia Gi Group S.P.A A tempo pieno

    HiRevo LifeScience è la specializzazione di Gi Group dedicata alla Ricerca e Selezione di profili in ambito Operation, Quality, Regulatory, R&D, Clinical Research e Sales & Marketing dei settori Farmaceutico e Medicale.Per rafforzamento del team di multinazionale operante nel settore della diagnostica molecolare, in particolare di soluzioni e test...

Clinical Research Associate

3 mesi fa

Bagni Di Tivol, Italia Novo Nordisk Pharma A tempo pieno
Are you passionate about managing clinical trial sites and ensuring adherence to regulatory requirements? Do you want to contribute to making Novo Nordisk the preferred partner in clinical trials? If so, we have an exciting opportunity for you to join our team as a Clinical Research Associate (CRA). Apply today for a life-changing career.The Position The CRA is responsible for managing clinical trial sites at every stage of the clinical trial process in accordance with the Company’s policies and procedures, relevant legislation, and ICH GCP requirements, whilst maintaining the standards of the Novo Nordisk Way.Main accountabilities of the role:Primary point of contact between site staff and Novo Nordisk, act as a site manager and an ambassador for the company and contributes to making Novo Nordisk the preferred partner in clinical trials;Overall site management, including site monitoring and remote monitoring as applicable;Ensure that trial site staff are properly trained to conduct the trial(s), provide necessary training, and identify and flag any development areas and implement mitigations;Managing trial sites to meet patient recruitment and retention target, aimed at successful completion of the clinical programme;Contribute to or lead selection of sites, in collaboration with CDC and local colleagues such as Line Managers and Medical Affairs. Qualifications To be eligible for this role, you need to hold a bachelor’s degree in life science (preferably in Biotechnology, Pharmacy, Chemistry, Biology, CTF) and to have a working experience of a minimum of 1 year of independent monitoring. You also meet the following requirements:You are Fluent in both Italian and English;Knowledge of clinical trial methodology;Good communication skills;Knowledge of the clinical trials environment – ICH GCP, regulatory issues, SOPs;Good working knowledge of electronic clinical trials systems – CTMS, EDC, IWRS, electronic TMF;Basic GCP qualification. About the Department CDC Italy is part of Region South East Europe, Middle East and Africa (SEEMEA) and is a new set-up of clinical organization in Novo Nordisk Italy. CDC Italy is responsible for conducting clinical trials within the country, providing clinical trial management and administration supporting the local teams. You will work in our Clinical, Medical and Regulatory (CMR) department at Novo Nordisk, that is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies, to providing medical education and collecting data to support efficacy and new product development, CMR is involved. In relation to Clinical Operations Italy is organised with a dedicated Clinical Development Centre (CDC) which is part of the CMR department.

Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.

Contact If you believe you are qualified, and cannot wait to take the challenge, please upload your motivation letter, CV and relevant documentation directly via our online application tool.Deadline Apply before July 1, 2024. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.Please apply to the role via our online platform, as we don’t accept directly sent CVs. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.