Clinical Research Associate

All vacancies of AustraliaHealthcare & MedicalClinical Research Associate

Acting as the primary link between sites and sponsor.

Summary about this job

Clinical/Medical Research

Company: Novotech (Australia) Pty Limited

Location: Sydney

Work type: Full Time

Salary: n\a

Phone: +61-8-2337-6579

Fax: +61-2-1502-6582

E-mail: n\a

Site:

Detail information about job Clinical Research Associate. Terms and conditions vacancy

Novotech is internationally recognised as the leading independent and full service contract research organisation (CRO) in the Asia Pacific region. We provide a wide range clinical development services across all research phases and therapeutic areas; and have been instrumental in the success of hundreds of Phase I – IV clinical trials throughout the Asia Pacific.

Powered by the highest quality people, Novotech strives to set the benchmark for both business and clinical trial performance.

Our people are one of our key strengths. We value our people and recognise the work they do. We are lucky to have the best people and talent from across the Asia Pacific region work together to deliver to clinical trial success for our clients.

Our people and those we look to recruit have an attitude of making things happen. They are problem solvers, driven with a focus on delivering quality, accountability and a high level of performance.

About the position 

Due to a strong project pipeline and an influx of client work, we are currently seeking a talented Clinical Research Associate to join our Sydney team as a CRAII, CRAIII or SCRA.  

Core responsibilities:

Acting as the primary link between sites and sponsor, you will be responsible for:

  • Acting as a site manager to ensure that clinical trials are conducted and documented as per ICH GCP guidelines, global and local regulatory requirements and Novotech/Client SOPs;
  • Providing mentorship to less experienced staff;
  • Providing support to the project manager as required; and
  • Performing site selection visits to ensure sites have adequate resources to conduct studies.

Required Qualification(s):

  • Tertiary qualifications in clinical or life sciences related field (relevant experience/qualifications in similar professions may also be considered);

Required Professional Experience:

  • At least 18 months of independent monitoring experience;
  • Solid knowledge of GCP, national and international regulations and a sound understanding of how they apply to you;
  • Excellent interpersonal and team skills with a genuine commitment to contributing to the development of innovative treatments;
  • Previous experience in monitoring oncology trials would be highly desirable; and
  • A strong track record of performing visits to sites according to the Clinical Monitoring Plan.

Opportunities and benefits

To deliver clinical trial and research excellence for our clients, our people are 'best in class'.

At Novotech, we seek and nurture people with exceptional talent. We are committed to providing our people with regular internal and external training, a competitive bonus structure and a supportive work environment. We are also focused on providing our people with a wide variety of career growth and development opportunities.

For more information about where your next career step at Novotech might take you, visit http://novotech-cro.com/novotech-careers

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