In-Demand Clinical research associate/senior Jobs

Clinical Research Associate/Senior
Pfizer —Remote
- Weekend availability
- Nursing
- Patient monitoring
- Master's degree
- Parental leave
- Life insurance
19h
Senior/Clinical Research Associate
Precision for Medicine —Sydney NSW
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
Senior/Clinical Research Associate
Precision Medicine Group —Brisbane QLD
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Research Associate II
PSI CRO —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
10d
Senior Clinical Research Associate - CNS/Early Phase - Australia - Remote
Worldwide Clinical Trials —Remote
- Full-time
- Nursing
- Microsoft Office
- Bachelor's degree
Sr. Clinical Research Associate (Australia)
Alimentiv —Remote
- $58,000 - $96,500 a year
- Full-time
- Patient monitoring
- AI
- Communication skills
Quick Apply
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 Specialist, Research Technology
Deakin University —Melbourne VIC
- $143,627 - $152,229 a year
- Full-time
- Hybrid work
- Research
- Analysis skills
- University
- Parental leave
10d
Lecturer or Senior Lecturer - Physiotherapy Clinical Placement Coordinator
Deakin University —Burwood VIC
- $122,391 - $171,602 a year
- Full-time
- Hybrid work
- Master's degree
- University
- Parental leave
Senior Clinical Research Associate I (SCRA1) - Sydney, Melbourne, Adelaide or Brisbane
Fortrea —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
- No degree
- Opportunities for advancement
Senior Lecturer/Associate Professor in Linguistics
Macquarie University —Macquarie University NSW
- $155,236 - $205,067 a year
- Full-time
- Hybrid work
- Medicine
- Doctoral degree
- Research
- Employee assistance program
Senior Lecturer / Associate Professor (Scientist and Scholar Domain Lead)
Curtin University of Technology —Perth WA
- $144,512 - $191,099 a year
- Full-time
- Medicine
- Doctoral degree
- Laboratory experience
9d
Senior Lecturer / Associate Professor (Professionalism Panel Lead)
Curtin University of Technology —Perth WA
- $144,512 - $191,099 a year
- Part-time
- Medicine
- Management
- Doctoral degree
13d
Fellow - Research
St Vincent's Health Australia —Melbourne VIC
- $129,048.40 - $177,622.12 a year
- Overtime
- Medicine
Associate Professor (Research), Australian Centre for AI in Medical Innovation
La Trobe University —Bundoora VIC
- From $172,864 a year
- Full-time
- Doctoral degree
- Working with children
- Recruiting
6d
Global Study Management (Senior) Associate (Global CTA)
BeiGene —Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Patient monitoring
1d
Associate Professor in Rural and Remote Health
Flinders University —Nuriootpa SA
- $169,706 - $186,706 a year
- Full-time
- Doctoral degree
- Research
- University
9d
Postdoctoral Research Associate in Pain Neurobiology and Brain Imaging
University of Sydney —Camperdown NSW
- $113,634 - $117,936 a year
- Full-time
- Doctoral degree
- Research
- Analysis skills
2d
Research Assistant - Molecular Haematology
Peter MacCallum Cancer Centre —Parkville VIC
- $73,762 - $105,846 a year
- Full-time
- Laboratory
- Communication skills
- Annual leave
2d
Associate Elective Pre Admission Coordinator (EPAC) - Surgical Services - WCH
SA Health —Adelaide SA
- $107,487 - $114,917 a year
- Part-time
- Nursing
- Clinic
- Leadership
- Commuter assistance
- Employee assistance program
10d

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Clinical Research Associate/Senior

Pfizer -
Remote

Apply Now

Job Details

Full-time
19 hours ago

Benefits

Employee rewards program
Parental leave
Paid volunteer leave
Life insurance
Salary packaging

Qualifications

Nursing
Patient monitoring
Master's degree
Analysis skills
Presentation skills
Bachelor's degree
Driver Licence
Clinical trials
AI
Communication skills
FDA regulations

Full Job Description

Use Your Power for Purpose

Reporting to the ANZ GSSO Leadership, you will play a critical role in delivering high-quality clinical trials by partnering with investigator sites to ensure patient safety, regulatory compliance, and operational excellence. As a Senior Clinical Research Associate I you will serve as a trusted partner to investigators and study teams, leading site management and monitoring activities from study activation through closeout.

By building strong site relationships, proactively managing risks, resolving protocol-related issues, and supporting site performance, you will help accelerate the delivery of clinical research while maintaining the highest standards of quality and Good Clinical Practice. Working closely with Site Care Partners and cross-functional study teams, your expertise will contribute to successful enrollment, data integrity, database release, and the generation of evidence that advances innovative medicines for patients worldwide.

What You Will Achieve

In this role, you will:

Lead site management and monitoring activities across assigned clinical trial sites, ensuring studies are conducted in accordance with protocol, Good Clinical Practice (GCP), regulatory requirements, and Pfizer standards.
Serve as the primary point of contact for investigator sites, building strong partnerships to support high-quality study delivery and successful trial outcomes.
Manage site operations from study start-up through closeout, ensuring key milestones, timelines, and quality objectives are achieved.
Conduct onsite, remote, and risk-based monitoring activities, including site initiation, routine monitoring visits, and closeout visits.
Partner with Site Care Partners and cross-functional study teams to identify and mitigate risks, resolve site issues, and drive operational excellence.
Support patient recruitment and enrollment efforts by collaborating with investigators and study teams to address site-level challenges and implement recruitment strategies.
Provide protocol guidance, training, and coaching to investigator site personnel to ensure compliance, quality execution, and patient safety.
Develop and maintain strong scientific and operational knowledge of study protocols, investigational products, and therapeutic areas to effectively support investigators and site teams.
Drive the identification, escalation, and resolution of site quality, compliance, and data integrity issues, including implementation of corrective and preventive actions (CAPAs).
Monitor and support patient safety activities, including adverse event and serious adverse event reporting and follow-up.
Ensure timely completion and maintenance of essential study documentation, trial records, and regulatory compliance requirements throughout the study lifecycle.
Contribute to continuous improvement initiatives by mentoring junior CRAs, sharing best practices, and participating in local and regional process improvement projects.

Here Is What You Need (Minimum Requirements)

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Proficiency in English, both written and verbal
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required

Bonus Points If You Have (Preferred Requirements)

Master's degree with experience in early drug development.
Ability to manage multiple projects simultaneously
Strong analytical and problem-solving skills
Excellent communication and presentation skills
Experience using common AI tools, including generative technologies such
as Microsoft Copilot or Gemini, to support problem solving and enhance

At Pfizer we care about our colleagues’ wellbeing and offer a range of great benefits for them, including:

Paid parental leave
Access to Health & Wellness apps
Career Growth Experiences program
Recognition & rewards program
Paid volunteer days
Life Insurance Benefits
Pfizer Learning Academy access to top content providers
Access to flu vaccines & skin checks
Options to purchase additional leave
Salary packaging & novated lease options

Benefits listed may vary depending on your position and location and may be subject to change.

Pfizer Australia and New Zealand’s diverse workforce represents the patients we serve and the communities in which we operate. With a focus on Diversity, Equity & Inclusion (DE&I), Pfizer ANZ ensures our people are heard and cared for. We offer engagement opportunities in both Colleagues Resource Groups (CRGs) and workstreams across: Culture and Tradition, Reconciliation @ Pfizer (RAP), Gender Equity (GEN), Disability and through the Out Pfizer Employee Network (OPEN) for our LGBT + colleagues and allies.

If you require reasonable adjustment during your application, please reach out to the Talent Acquisition Manager.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Medical

Apply Now

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clinical research associate/senior jobs

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