Crea un profilo in modo da poter essere trovato dalle aziende, ottenere offerte di lavoro più adatte alle tue esigenze e candidarti più velocemente.
  • Cerca lavoro
  • Preferiti
  • Crea CV
    Novità
  • Stipendi
  • Iscrizioni

Sr. Clinical Research Associate

ICON plc

Milano
  • Lavoro da remoto

Sr. Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

Offerta di lavoro pubblicata un mese fa
Offerte di lavoro simili
  •  ...Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of... 
    Consigliato
    Lavoro da remoto

    ICON plc

    Milano
    24 giorni fa
  • 55.000 € - 65.000 €

     ...Senior CRA who is passionate about oncology research and looking to join a highly skilled and...  ...Research in Oncology (TRIO) is a global clinical research organization dedicated to...  ...looking for a Senior Clinical Research Associate   to join our Monitoring Resources team.... 
    Consigliato
    Tempo pieno
    Lavoro da casa
    Orario flessibile

    Translational Research in Oncology

    Milano
    11 giorni fa
  •  ...Senior Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future... 
    Consigliato
    Lavoro da remoto

    ICON plc

    Milano
    17 giorni fa
  •  ...Experienced Clinical Research Associate, Italy Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices... 
    Consigliato
    Tempo pieno
    Auto aziendale
    Orario flessibile

    IQVIA

    Milano
    24 giorni fa
  •  ...to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating...  ...• Complete appropriate therapeutic, protocol and clinical research training to perform job duties. • Gain experience in study... 
    Consigliato
    Tempo pieno

    IQVIA

    Milano
    6 giorni fa
  •  ...contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (...  ...class B IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the... 
    Tempo pieno
    Lavoro da casa
    Orario flessibile

    IQVIA

    Milano
    un mese fa
  •  ...resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research... 
    Lavoro da remoto
    Tempo pieno
    Orario flessibile
    Dal lunedì al venerdì
    Milano
    8 giorni fa
  • 32.000 €

     ...scientifico preferibile o equivalente e/o esperienza pregressa in ambito clinico o medical setting, ad es. Study Coordinator, assistente di...  ...; • Buona conoscenza dei protocolli clinici, delle Good Clinical Practice (GCP) e degli aspetti regolatori e gestionali della ricerca... 
    Tempo pieno
    Impiego permanente
    Somministrazione

    Adecco Italia

    Milano
    1 giorno fa
  •  ...accurate, nuove e rilevanti per i prodotti della propria area terapeutica, come lo stato d’avanzamento della patologia, i bisogni clinici non “soddisfatti” (unmet medical need), così come le nuove indicazioni terapeutiche e le nuove pratiche nella cura dei pazienti tramite... 
    Contratto con partita IVA
    Remoto
    Milano
    1 giorno fa
  •  ...Liaison (MSL). You'll be the key scientific point of contact for clinical trial sites-supporting site engagement, education, and patient...  ...: Provide field-based medical support to clinical research programs in oncology. Deliver credible, balanced presentations... 
    Tempo pieno

    IQVIA

    Milano
    28 giorni fa
  •  ...Institute of Oncology Milan, Italy Two postdoctoral research fellow positions are available in the Hormone-Related Cancers...  ...molecular mechanisms of tumor aggressiveness and discovering clinically relevant biomarkers and therapeutic vulnerabilities in epithelial... 
    Lavoro ibrido

    IEO - European Institute of Oncology

    Milano
    17 giorni fa
  • 35.000 € - 45.000 €

     ...settore dei dispositivi medici. La figura ricercata La risorsa dovrà occuparsi delle seguenti attività: * supporto tecnico e clinico all'utilizzo delle tecnologie al personale medico ospedaliero di riferimento; * assistenza in Sala Operatoria durante le procedure... 
    Impiego permanente

    Page Personnel

    Milano
    18 giorni fa
  • 24.000 € - 30.000 €

     ...cliente accessibile dando un follow-up comodo e a distanza. La risorsa sarà il punto di riferimento per l'ottimizzazione dei processi clinici e operativi, supportando l'implementazione di procedure, tecnologie e progetti finalizzati al miglioramento delle performance delle... 

    Impress

    Milano
    9 giorni fa