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Clinical Study Administrator

Location Macquarie Park, New South Wales, Australia Job ID R-100928 Date posted 23/02/2021

Clinical Study Administrator (CSA)

Enjoy supporting others as an administrator and wanting to join a global organisation as a career Clinical Study Administrator?

A new opportunity on a fixed term contract with a view for extension/permanency for the right candidate!

Who Are You

What are you looking for in your next clinical research opportunity?

  • An opportunity to showcase your passion within administration and pursuing a career as a CSA

  • An encouraging office environment with flexibility in the way you work

  • The opportunity for growth and development in a team which accepts your ‘above the line’ thinking and feedback

  • Working with Local Clinical Project Managers who can provide real-time support and decisions

  • A team who is driven by the needs of patients to improve clinical trials

  • A company who is committed to improving our world through sustainability initiatives including 25 million trees planted in Australia by 2025

  • A company investing and growing in Australian manufacturing and who exports medicines to the world

If the above statements sound amazing, then this role might be the role for you!

Who Are We

We are a hard-working, fun, fast paced, supportive, cake-loving (with free gym access) team. We are continuously evolving and adapting to create new and better ways of working across clinical research and development. We want to support each other to be as efficient as possible to drive work life balance. We are undergoing expansion and with so many roles locally and globally, we provide opportunities to drive your development and growth your way. The team has grown by 60% in just 2020 alone, and still growing. Our pipeline and projects are continuously growing, and we want you to join us!

Opportunities can be tailored to your career interests. We provide onsite parking; extra Christmas leave days; flexibility; clean and green working environment. We also have a focus on sustainability

Your new role

This role would be suitable for someone who has a passion within administration. You enjoy supporting others through your immaculate attention to detail and hard-working attitude.

As our new CSA, you will assist in the coordination and administration of the study activities from start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study results to time, cost and quality objectives.

To be successful in this role you will have excellent knowledge of Clinical Study Management and have experience working in a similar capacity.

You Will:

  • Support clinical trials from study feasibility through to study results

  • Work with international clinical trials across Australia and New Zealand

  • Join a local inhouse pharma clinical research team where we are the Sponsor. We are driven to provide the best support possible to our sites and partners

  • Continually learn and strive to improve

  • Work with a dynamic and encouraging team where a risk-based approach to monitoring and everything we do is being accepted. Where focusing on what really matters is valued

Requirements for the position

  • Experience that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.

  • Previous administrative experience preferably in the medical/ life science field

  • Proven interpersonal and administrative skills

  • Highly proficient in computer programs

  • Good knowledge of spoken and written English

  • Full working rights (we are not able to sponsor for this role)

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

50056677 C CDSM R&D BioPharmaceuticals

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Glassdoor logo Rated four stars on Glassdoor

Great culture, great work assignments, supportive management. Rotation opportunity within the company. They value inclusion and diversity.