In-Demand Clinical compliance Jobs in Wollert Vic

Independent Clinical Research Associate (CRA) / Clinical Monitor – Australia
CEBIS USA —Parkville VIC
- Contract
- Nursing
- Patient monitoring
- Bachelor's degree
Quick Apply
7d
Clinical Trials Coordinator
Austin Health —Heidelberg VIC
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Health insurance
1d
Clinical Research Associate
The Royal Melbourne Hospital —Parkville VIC
- Part-time
- Patient monitoring
- Research
- Communication skills
2d
Clinical Data Analyst
The Royal Children's Hospital —Parkville VIC
- $114,436.40 - $124,912.84 a year
- Full-time
- Hybrid work
- Administrative experience
- SQL
- EMR systems
- Employee assistance program
10h
Work Integrated Learning & Compliance Officer
University of Melbourne —Parkville VIC
- $86,943 - $99,864 a year
- Full-time
- Microsoft Office
- Experience working with children
- No degree
- Health insurance
- Parental leave
6d
Study Coordinator
The Royal Melbourne Hospital —Parkville VIC
- Part-time
- Vital signs
- Research
- Communication skills
9d
Complex Needs Female Support Worker
JESSICARE PTY LTD —Doreen VIC
- $45 - $50 an hour
- Call employer
- Patient monitoring
- First Aid Certification
- In-person
Quick Apply
8d
Consultant - Medical Informatics
The Royal Children's Hospital —Parkville VIC
- Up to $11,500 a year
- Part-time
- Hybrid work
- Medicine
- EMR systems
- Epic
- Employee assistance program
2d
Quality Officer
Dovida —Coburg North VIC
- $90,000 a year
- Full-time
- Analysis skills
- Communication skills
Quick Apply
14d
Program Evaluation Assistant
The Royal Children's Hospital —Parkville VIC
- $69,438.72 - $76,764.48 a year
- Part-time
- Administrative experience
- No degree
- Employee assistance program
2d
Project Support Officer
The Royal Children's Hospital —Parkville VIC
- $96,570.76 - $106,759.12 a year
- Part-time
- Hybrid work
- EMR systems
- Epic
- AI
- Employee assistance program
3d
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
10d
Team Leader - Allied Health
Early Start Australia —South Morang VIC
- Full-time
- Clinic
- First Aid Certification
- Leadership
- Annual leave
Quick Apply
2d
Insectary Lead
The Walter and Eliza Hall Institute of Medical Research —Parkville VIC
- $108,119 - $117,039 a year
- Full-time
- Research
- Organisational skills
- Communication skills
Clinical Outcome Partner
Baptcare —Lalor VIC
- $64.95 an hour
- Full-time
- Data analysis skills
- Leadership
- Communication skills
Chief Nursing Information Officer (CNIO)
The Royal Children's Hospital —Parkville VIC
- Up to $11,500 a year
- Full-time
- Nursing
- Patient monitoring
- Master's degree
- Employee assistance program
- Gym membership
2d
Chief Medical Information Officer
The Royal Children's Hospital —Parkville VIC
- Up to $11,500 a year
- Part-time
- Medicine
- Patient monitoring
- Research
- Employee assistance program
- Gym membership
3d
NDIS Administration Coordinator
The Royal Children's Hospital —Parkville VIC
- $87,003.80 - $96,181.28 a year
- Part-time
- Hybrid work
- Customer service
- Administrative experience
- Front desk
- Employee assistance program
10h
RUSON- Nursing Workforce Unit
The Royal Children's Hospital —Parkville VIC
- Up to $11,500 a year
- Part-time
- Nursing
- Bachelor's degree
- Communication skills
- Employee assistance program
- Gym membership
1d
Social Worker
The Royal Children's Hospital —Parkville VIC
- $90,235 - $103,724 a year
- Full-time
- Discharge planning
- Social Work
- Employee assistance program
1d

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

CEBIS USA
Parkville VIC

Quick Apply

Job Details

Contract
7 days ago

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 compliance jobs in wollert vic

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

Clinical Trials Coordinator

Clinical Research Associate

Clinical Data Analyst

Work Integrated Learning & Compliance Officer

Study Coordinator

Complex Needs Female Support Worker

Consultant - Medical Informatics

Quality Officer

Program Evaluation Assistant

Project Support Officer

Medical Scientist – Clinical Trials Genome Analyst

Team Leader - Allied Health

Insectary Lead

Clinical Outcome Partner

Chief Nursing Information Officer (CNIO)

Chief Medical Information Officer

NDIS Administration Coordinator

RUSON- Nursing Workforce Unit

Social Worker

I want to receive the latest job alert for clinical compliance in wollert vic

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