In-Demand Clinical trial Jobs in Wantirna South Vic

Independent Clinical Research Associate (CRA) / Clinical Monitor – Australia
CEBIS USA —Parkville VIC
- Contract
- Nursing
- Patient monitoring
- Bachelor's degree
Quick Apply
Clinical Trials Assistant
Monash Health —Clayton VIC
- Full-time
- Marketing
- Microsoft Office
- Administrative experience
3d
Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)
Medpace, Inc. —South Yarra VIC
- Full-time
- Microsoft Excel
- Management
- Doctoral degree
- Health insurance
- Annual leave
Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Clinical Trial Data Administrator
Peter MacCallum Cancer Centre —Parkville VIC
- $69,438 - $76,764 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer Science
- Annual leave
2d
Clinical Sales Specialist
Fresenius Medical Care —Scoresby VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
9d
Research Assistant
Eastern Health —Richmond VIC
- Full-time
- Google Suite
- Microsoft Excel
- Research
- Health insurance
- Annual leave
11d
Regulatory Submissions Coordinator
Medpace, Inc. —South Yarra VIC
- Full-time
- Research
- Microsoft Office
- Bachelor's degree
- Health insurance
- Annual leave
Clinical Study Startup Lead | 12 Months Fixed Term Contract
Roche —Melbourne VIC
- Contract
6d
Clinical Trial Coordinator (Radiation Oncology)
Austin Health —Heidelberg VIC
- Part-time
- Nursing
- Management
- Microsoft Office
- Health insurance
9d
Medical Scientist – Clinical Trials Genome Analyst
Peter MacCallum Cancer Centre —Parkville VIC
- $94,479 - $106,907 a year
- Weekend availability
- Hybrid work
- Laboratory
- Doctoral degree
- Customer service
- Annual leave
Clinical Trial Psych Rater - Mandarin Speaking
IQVIA —Melbourne VIC
- Part-time
- Remote
- Medicine
- Doctoral degree
- English
- Work from home
1d
Clinical Trial Manager (FSP)
Thermo Fisher Scientific —Melbourne VIC
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Parental leave
- Employee assistance program
22h
Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Specialist - TAVR - AU
Anteris Technologies —Melbourne VIC
- $145,000 - $200,000 a year
- Remote
- Nursing
- Anatomy knowledge
- Bachelor's degree
- Annual leave
Quick Apply
Clinical Research Associate
The Royal Melbourne Hospital —Parkville VIC
- Part-time
- Patient monitoring
- Research
- Communication skills
9d
Quality Assurance Assistant
Cencora —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Research Assistant
HammondCare —Malvern VIC
- Full-time
- Vital signs
- Research
- Administrative experience
- Employee assistance program
17h
Clinical Trials Coordinator
Victorian Government —Melbourne VIC
- Part-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Health insurance
8d
Technical Writer (Casual)
BioAgilytix —Melbourne VIC
- Contract
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply

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Independent Clinical Research Associate (CRA) / Clinical Monitor – Australia

CEBIS USA
Parkville VIC

Quick Apply

Job Details

Contract

Qualifications

Nursing
Patient monitoring
Bachelor's degree
Driver Licence
Pharmacy
Communication skills

Full Job Description

Independent Clinical Research Associate (CRA) / Clinical Monitor – Australia

Location: Australia (Remote with travel as required)

Employment Type: Contract / Freelance

About Us

We are a U.S.-based Clinical Research Organization (CRO) dedicated to providing high-quality clinical trial management and clinical operations support to pharmaceutical, biotechnology, and medical device companies. As we continue to expand our global network, we are seeking an experienced Independent Clinical Research Associate (CRA) / Clinical Monitor based in Australia to support upcoming Phase II–IV clinical trials across multiple therapeutic areas.

This role offers an exciting opportunity to work collaboratively with international sponsors, investigators, and project teams while contributing to the successful execution of clinical research studies throughout Australia.

Position Summary

The Clinical Research Associate (CRA) will be responsible for monitoring assigned clinical trial sites to ensure studies are conducted in accordance with the study protocol, ICH-GCP guidelines, applicable regulatory requirements, and sponsor Standard Operating Procedures (SOPs). The CRA will serve as the primary point of contact between the sponsor/CRO and investigative sites, providing ongoing support to ensure subject safety, data quality, and regulatory compliance.

Key Responsibilities

· Conduct Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), Routine Monitoring Visits (RMVs), and Close-Out Visits (COVs).

· Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, and local regulatory requirements.

· Perform Source Data Verification (SDV) and Source Data Review (SDR) to ensure data accuracy, completeness, and integrity.

· Review informed consent documentation, eligibility criteria, protocol compliance, and investigational product accountability.

· Identify protocol deviations and support sites with corrective and preventive actions.

· Prepare monitoring reports, follow-up letters, and other required documentation within established timelines.

· Collaborate with investigators, study coordinators, project managers, data management teams, and sponsors throughout the study lifecycle.

· Support regulatory and essential document review as required.

· Maintain effective communication with assigned investigative sites to facilitate successful study execution.

· Participate in investigator meetings, sponsor meetings, and study-specific training as required.

Qualifications

· Bachelor's degree in Life Sciences, Nursing, Pharmacy, or another healthcare-related discipline.

· Previous experience as a Clinical Research Associate (CRA) or Clinical Monitor.

· Strong understanding of ICH-GCP, Australian clinical research regulations, and ethical guidelines.

· Experience conducting independent monitoring visits across multiple sites.

· Excellent written and verbal communication skills.

· Strong organizational, problem-solving, and time management abilities.

· Ability to travel within Australia as required.

Preferred Experience

Experience monitoring studies in one or more of the following therapeutic areas is preferred:

· Oncology

· Neurology

· Dermatology

· Endocrinology/Metabolic Disorders

· Women's Health

· Men's Health

· Cardiovascular

· Infectious Diseases

· Vaccines

· Rare Diseases

Experience with electronic data capture (EDC), CTMS, and eTMF systems platforms is desirable.

What We Offer

· Opportunity to collaborate with an expanding U.S.-based CRO on international clinical trials.

· Flexible contract engagement with competitive compensation.

· Exposure to diverse therapeutic areas and global sponsor programs.

· Opportunity to build a long-term relationship as our Australian clinical operations network continues to grow.

· Collaborative, quality-focused working environment with experienced clinical operations professionals.

How to Apply

· If you are interested in this opportunity, please submit:

· Your updated CV

· Current location within Australia

· Summary of therapeutic area experience

· Monitoring experience (SQV, SIV, RMV, COV)

· Availability (full-time, part-time, or freelance)

Application Question(s):

Do you have a valid driver's license and reliable transportation to travel to and from assigned work locations?
Are you currently residing in Australia and legally authorized to work in Australia?
Do you have working knowledge of ICH-GCP guidelines and Australian clinical research regulations?
Have you independently conducted Site Qualification Visits (SQV), Site Initiation Visits (SIV), Routine Monitoring Visits (RMV), and Close-Out Visits (COV)?

Willingness to travel:

50% (Required)

Work Location: In person

Quick Apply

Refine Your Search

clinical trial jobs in wantirna south vic

Independent Clinical Research Associate (CRA) / Clinical Monitor – Australia

Clinical Trials Assistant

Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)

Clinical Research Associate

Clinical Trial Data Administrator

Clinical Sales Specialist

Research Assistant

Regulatory Submissions Coordinator

Clinical Study Startup Lead | 12 Months Fixed Term Contract

Clinical Trial Coordinator (Radiation Oncology)

Medical Scientist – Clinical Trials Genome Analyst

Clinical Trial Psych Rater - Mandarin Speaking

Clinical Trial Manager (FSP)

Senior / Clinical Research Associate

Clinical Specialist - TAVR - AU

Clinical Research Associate

Quality Assurance Assistant

Research Assistant

Clinical Trials Coordinator

Technical Writer (Casual)

I want to receive the latest job alert for clinical trial in wantirna south vic

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