In-Demand Clinical associate Jobs in Macquarie University Nsw

Clinical Research Associate - Biopharma
AstraZeneca —Macquarie Park NSW
- Contract
- Patient monitoring
- Bachelor's degree
- No degree
13d
Clinical Research Associate
IQVIA —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Local Study Associate Director (Clinical Project Manager) - Biopharma
AstraZeneca —Macquarie Park NSW
- Contract
- Management
- Patient monitoring
- Bachelor's degree
13d
Senior/Clinical Research Associate
Precision for Medicine —Sydney NSW
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
Clinical Associate
Globus Medical —Sydney NSW
- Full-time
- Anatomy knowledge
- Bachelor's degree
- No degree
Senior / Clinical Research Associate
IQVIA —North Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Engagement Associate
Cochlear Ltd —Macquarie Park NSW
- Full-time
- Sales
- Customer service
- Databases
Clinical Trial Assistant
Cochlear Ltd —Sydney NSW
- Full-time
- Hybrid work
- Nursing
- Management
- Microsoft Office
10d
Sr Clinical Research Associate II - FSP, Sydney
Fortrea —Sydney NSW
- Full-time
- Management
- Patient monitoring
- Customer service
10d
Sr Clinical Research Associate Contractor (Australia)
Allucent —Sydney NSW
- Full-time
- Remote
- Patient monitoring
- Master's degree
Quick Apply
14d
Senior/Clinical Research Associate
Precision Medicine Group —Sydney NSW
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Research Associate II - Sydney
Fortrea —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
Project Support Associate/Senior Project Support Associate
Southern Star Research —North Sydney NSW
- Full-time
- Hybrid work
- Research
- Microsoft Office
- Organisational skills
Quick Apply
Senior Regulatory Affairs Associate
Solventum —North Ryde NSW
- Full-time
- Administrative experience
- Bachelor's degree
- Communication skills
Associate Product Specialist (Contract)
Medtronic —Macquarie Park NSW
- Full-time
- CRM software
- Marketing
- Salesforce
2d
Clinical Trial Coordinator II
Thermo Fisher Scientific —Sydney NSW
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Parental leave
- Employee assistance program
Sr Clinical Research Associate I Sydney, Melbourne, or Perth
Fortrea —Sydney NSW
- Full-time
- Management
- Patient monitoring
- Administrative experience
14d
Senior Clinical Research Associate
Thermo Fisher Scientific —Sydney NSW
- Full-time
- Laboratory
- Patient monitoring
- Research
- Relocation assistance
- Parental leave
RAS Associate
Reckitt —Sydney NSW
- Employee assistance program
- Life insurance
Freelance Senior Clinical Research Associate
TFS HealthScience —Sydney NSW
- Contract
- Remote
- Nursing
- Patient monitoring
- English
Quick Apply
1d

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Clinical Research Associate - Biopharma

AstraZeneca -
Macquarie Park NSW

Apply Now

Job Details

Contract | Fixed term
13 days ago

Qualifications

Patient monitoring
Bachelor's degree
Communication skills

Full Job Description

Location Macquarie Park, New South Wales, Australia Job ID R-257824 Date posted 06/08/2026

We currently building out our Biopharma Site Management and Monitoring team, and we have a vacancy for a Clinical Research Associate available now based in Sydney.

At AstraZeneca, we’re united by a bold ambition: to transform patients’ lives through science. Across BioPharma and Oncology, we design and deliver high‑quality, patient‑centric clinical trials that translate deep biology into breakthrough medicines in cardiovascular, renal & metabolism, respiratory & immunology, and cancers where the need is greatest.

As a Clinical Research Associate, you will own site activation and performance, direct risk-based monitoring to where it matters most, and safeguard patient safety and data integrity. You will partner with investigators, shape inspection readiness, and apply a forward-looking approach that challenges the status quo and accelerates launches. How will you use your judgment and influence to turn a promising protocol into a reliable, scalable trial outcome. Initially this role is a 12 Month Contract but there is potential scope for the role to be ongoing for the right person.

What you’ll do

Identify and evaluate sites and investigators, build collaborative relationships, and drive activation, enrolment and sustained performance.
Coordinate EC/IRB and health‑authority submissions, secure and maintain approvals, and manage essential documents to keep studies inspection‑ready from day one.
Train and support site teams on ICH‑GCP and RbQM, embed compliance routines, and coach toward audit and inspection readiness.
Conduct remote and onsite monitoring visits; perform Source Data Review (SDR), Source Data Verification (SDV) and Case Report Form (CRF) review; manage data queries; and adjust monitoring intensity based on risk signals.
Ensure timely reporting of Serious Adverse Events (SAEs); proactively identify, escalate and resolve quality issues in line with AstraZeneca SOPs.
Maintain CTMS and eTMF accuracy; manage study drug supplies and accountability; and deliver clear, timely monitoring reports and follow‑up.

Essential for the role

Sydney Based
Minimum of 3-5 Years experience as a Clinical Research Associate
Bachelor’s degree in a life science or related field (or equivalent experience).
Solid understanding of the drug development process, ICH‑GCP and relevant country regulations.
Experience in site selection, activation and monitoring (remote and onsite) with strong documentation discipline.
Proficiency with CTMS/eTMF and data‑query management; familiarity with SDR/SDV/CRF review.
Strong communication, stakeholder management and problem‑solving skills; ability to work independently and as part of a cross‑functional team.
Willingness to travel for site monitoring; fluency in written and spoken business‑level English.

Desirable for the role

Experience across Biopharma trials, in particular metabolic, cardiology and respiratory
Hands‑on use of RbQM analytics/dashboards to prioritise monitoring and remediation.
Proven contribution to accelerated start‑up timelines and efficient site activation.
Confidence in audits/inspections; track record coaching sites to readiness.
Comfort with remote monitoring tools, eSource/ePRO and data‑driven decision‑making.
Fluency in the local language in addition to English.

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare.

To Apply

Please apply with a resume and cover letter outlining your suitable skills and experience applicable to this role.

Where can I find out more?

Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/ Visit our website: www.astrazeneca.com.au

AstraZeneca in Australia has been formally recognised as an Employer of Choice for Gender Equality by the Workplace Gender Equality Agency (WGEA) and as a Gold Tier Employer within the Australian Workplace Equality Index (AWEI). Visit our ANZ Careers Page - www.astrazeneca.com.au/careers.html to learn more about our commitment to fostering a flexible, diverse, and inclusive environment.

We recognise that any recruitment process may present challenges, if there is anything we can do to make our recruitment process more accessible for you, please let us know via this Form

Ready to make an impact? Apply to register your interest today.

Date Posted

07-Aug-2026

Closing Date

21-Aug-2026

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 authorization and employment eligibility verification requirements.

Apply Now

Refine Your Search

clinical associate jobs in macquarie university nsw

Clinical Research Associate - Biopharma

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