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Fırsat Ayrıntıları

Senior / Clinical Research Associate

Son Başvuru Tarihi
October 10, 2026
Çalışma türü
Full time
Pozisyon Türü
Araştırmacı
Yayın Tarihi
September 22, 2026
Araştırma Alanı
Clinical
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Explicify özeti

İlan Özeti

Cochlear in Sydney is hiring a Senior Clinical Research Associate to support and expand its clinical monitoring function. The role involves acting as the primary contact for study sites, conducting monitoring visits, managing ethics submissions, delivering site training, and ensuring compliance through audits and file reviews. Candidates should have at least two years of CRA monitoring experience, strong stakeholder management, and the ability to work autonomously and handle conflict. The position offers the chance to shape the monitoring capability, work closely with a small team, and enjoy reduced travel compared to traditional CRA roles.

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Proje Açıklaması

Please submit your application as soon as possible, as we reserve the right to close this advertisement at any time.

Cochlear’s mission is to help people hear and be heard. As the global leader in implantable hearing solutions, Cochlear is dedicated to helping people with moderate to profound hearing loss experience a world full of sound. We aim to transform the way people understand and treat hearing loss and innovate to connect people with future technologies. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives. Learn and grow with us as we tackle the most complex challenges in helping more people to experience a lifetime of hearing.

The Opportunity

An exciting opportunity exists for a Senior / Clinical Research Associate (CRA) to support the delivery of clinical studies and help build Cochlear's clinical monitoring capability. As a key contact for clinical study sites, you will work closely with internal and external stakeholders, supporting the successful delivery of clinical studies. This role offers the opportunity to contribute to a growing function and play an active role in improving processes and ways of working.

The Responsibilities:

  • Act as the primary contact for internal and external study sites and manage site relationships throughout the study lifecycle.
  • Conduct monitoring activities including Pre-Study Visits, Site Initiation Visits, Interim Monitoring Visits and Close Out Visits.
  • Support study start-up activities, including ethics committee applications and study documentation requirements.
  • Deliver site training and ensure site staff are prepared to conduct studies in accordance with requirements.
  • Support audits, file reviews and other quality activities to ensure studies are conducted compliantly.
  • Contribute to the improvement and development of Cochlear's monitoring capability and support broader business activities where required.
  • About you

    As we grow our operations, we are looking for people who share our passion for delivering quality hearing solutions to our customers. To add value to Cochlear in this role, you'll be able to demonstrate the following skills and experience:

  • Solid clinical monitoring experience as a CRA, with at least 2 years of monitoring experience.
  • Experience with clinical trial submissions to Ethics Committees / Research Governance Units is desirable.
  • Strong stakeholder management and relationship-building skills.
  • Confidence managing conflict, negotiating outcomes and handling difficult conversations with key stakeholders.
  • Experience supporting clinical studies and working with study sites.
  • Ability to work autonomously, exercise sound judgement and manage ambiguity.
  • A proactive and action-oriented approach with a strong focus on accountability, meeting timelines and delivering results.
  • Flexibility to work within a small team environment and contribute beyond narrowly defined role boundaries when needed.
  • What makes this role unique

    This role provides the opportunity to help shape and strengthen Cochlear's monitoring capability as the organisation expands its clinical research activities. Working within a small team, you will have the opportunity to contribute ideas, influence improvements and take ownership of how the function evolves. You will work on end-to-end lifecycle study management with a small number of sites, allowing you to build strong relationships and enjoy significantly reduced travel compared with many traditional CRA roles

    If you feel that you have the skills and experience to be successful in this role and take on new challenges to build your career with Cochlear, please start your application by clicking the apply button below.

    #CochlearCareers

    How we recognise your contribution

    At Cochlear we value and welcome the unique contributions, perspectives, experiences, and backgrounds of our employees and aim to build a culture that celebrates and leverages these differences, creating a sense of belonging and enabling our people to realise their full potential. Through our internal programs and employee benefits, we aim to create an environment where our people will feel value and supported. Whether your focus is on continuous learning, professional development or simply finding an environment which enables you to thrive whilst balancing family or personal life commitments, then we have several programs in place to support you.

    For more information about Life at Cochlear, visit www.cochlearcareers.com


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