In-Demand Research coordinator Jobs in Parkville, Vic

Independent Clinical Research Associate (CRA) / Clinical Monitor – Australia
CEBIS USA —Parkville VIC
- Contract
- Nursing
- Patient monitoring
- Bachelor's degree
Quick Apply
Academic Placement Assessor (Academic Liaison Visitor)
Ikon —Melbourne VIC
- Part-time
- Research
- Communication skills
- Teaching
Quick Apply
Community and Stakeholder Engagement Coordinator
Jesuit Social Services —Sunshine VIC
- Part-time
- Employee assistance program
2d
Team Coordinator, Emergency Mental Health
The Royal Children's Hospital —Parkville VIC
- Up to $11,500 a year
- Part-time
- Hybrid work
- Supervising experience
- Hospital experience
- Employee assistance program
4d
Coordinator, Scheduling
University of Melbourne —Parkville VIC
- $6 - $109,163 a year
- Full-time
- Microsoft Excel
- Management
- University
- Health insurance
- Parental leave
13d
Study Coordinator
The Royal Melbourne Hospital —Parkville VIC
- Part-time
- Vital signs
- Research
- Communication skills
Regulatory Submissions Coordinator
Medpace, Inc. —South Yarra VIC
- Full-time
- Research
- Microsoft Office
- Bachelor's degree
- Health insurance
- Annual leave
Bone Transplant Donor Coordinator
Victorian Government —Melbourne VIC
- $123,906 a year
- Full-time
- Organisational skills
- Communication skills
- Annual leave
3d
Bone Transplant Donor Coordinator
The Royal Melbourne Hospital —Parkville VIC
- Full-time
- Organisational skills
- Communication skills
- Annual leave
3d
Study Coordinator
BioAgilytix —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
Linen Services Coordinator
The Royal Children's Hospital —Parkville VIC
- $87,003.80 - $96,181.28 a year
- Full-time
- Hybrid work
- Customer service
- Administrative experience
- Leadership
- Employee assistance program
2d
Administration Assistant - 12 month fixed term contract
Davies Collison Cave —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Parental leave
11d
Clinical Trials Coordinator
Victorian Government —Melbourne VIC
- Part-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Health insurance
11d
Research Assistant / Coordinator
FE fundinfo —Melbourne VIC
- Full-time
- Hybrid work
- Research
- Microsoft Office
- Administrative experience
Quick Apply
Premium Membership Coordinator
Essendon Football Club —Melbourne VIC
- Full-time
- Sales
- Parental leave
Quick Apply
Research Assistant
HammondCare —Malvern VIC
- Full-time
- Vital signs
- Research
- Administrative experience
- Employee assistance program
3d
Customer Engagement Manager
Incluso Services Pty Ltd —Coburg VIC
- Hybrid work
- Business development
- Organisational skills
- Communication skills
- Employee assistance program
Quick Apply
Marketing Coordinator - Rare Spares Campbellfield
Rare Spares —Campbellfield VIC
- Full-time
- Marketing
- Editing
- Time management
- Parental leave
- Employee assistance program
Quick Apply
Project Associate / Snr Project Associate
Avance Clinical —Melbourne VIC
- Full-time
- Nursing
- Analysis skills
- Bachelor's degree
Quick Apply
Operations Officer (Bundoora)
The Walter and Eliza Hall Institute of Medical Research —Bundoora VIC
- $78,121 - $82,911 a year
- Full-time
- Customer service
- Administrative experience
- Organisational skills
2d

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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

research coordinator jobs in parkville, vic

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

Academic Placement Assessor (Academic Liaison Visitor)

Community and Stakeholder Engagement Coordinator

Team Coordinator, Emergency Mental Health

Coordinator, Scheduling

Study Coordinator

Regulatory Submissions Coordinator

Bone Transplant Donor Coordinator

Bone Transplant Donor Coordinator

Study Coordinator

Linen Services Coordinator

Administration Assistant - 12 month fixed term contract

Clinical Trials Coordinator

Research Assistant / Coordinator

Premium Membership Coordinator

Research Assistant

Customer Engagement Manager

Marketing Coordinator - Rare Spares Campbellfield

Project Associate / Snr Project Associate

Operations Officer (Bundoora)

I want to receive the latest job alert for research coordinator in parkville, vic

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