In-Demand Associate medical science Jobs in Melbourne, Vic

Independent Clinical Research Associate (CRA) / Clinical Monitor – Australia
CEBIS USA —Parkville VIC
- Contract
- Nursing
- Patient monitoring
- Bachelor's degree
Quick Apply
13d
Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Analyst, Quality Control, Chemistry & Stability
Moderna, Inc. —Melbourne VIC
- Full-time
- Laboratory
- Bachelor's degree
- In-person
- Annual leave
Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)
Medpace, Inc. —South Yarra VIC
- Full-time
- Microsoft Excel
- Management
- Doctoral degree
- Health insurance
- Annual leave
13d
Associate Scientist
CSL Behring —Melbourne VIC
- Full-time
- Laboratory
- Microsoft Excel
- Writing skills
1d
Discipline Lead, Medical Radiations
RMIT University —Melbourne VIC
- $176,883 - $227,847 a year
- Full-time
- Doctoral degree
- Research
- Supervising experience
(Fixed-Term) Manufacturing Associate
Moderna, Inc. —Melbourne VIC
- Overtime
- Bachelor's degree
- No degree
- In-person
- Annual leave
3d
Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Quality Assurance Filling x 2
CSL Behring —Broadmeadows VIC
- Full-time
- Engineering
- Bachelor's degree
- Manufacturing
5d
Associate Data Scientist
Culture Amp —Melbourne VIC
- Master's degree
- SQL
- Machine learning
- Health insurance
- Parental leave
Senior Clinical Research Associate - FSP Melbourne / Sydney
Fortrea —Melbourne VIC
- Full-time
- Management
- Patient monitoring
- Administrative experience
13d
Test Analyst
Conduent Victoria Ticketing System Pty Ltd —Melbourne VIC
- Full-time
- Azure
- Computer Science
- Analysis skills
Associate Territory Manager - Trauma
Stryker —Melbourne VIC
- Full-time
- Sales
- English
- Bachelor's degree
- Health insurance
- Parental leave
Senior Associate Quality Assurance Value Stream
CSL Behring —Broadmeadows VIC
- Full-time
- Engineering
- Bachelor's degree
- Manufacturing
5d
Senior Manager / Assoc Director, Quality Assurance
Gilead Sciences —Melbourne VIC
- Weekend availability
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Research Assistant - Physical Sciences
Peter MacCallum Cancer Centre —Parkville VIC
- $44,257 - $63,507 a year
- Hybrid work
- Doctoral degree
- Computer Science
- Research
- Annual leave
15h
Associate Feasibility Director
IQVIA —Melbourne VIC
- Full-time
- Remote
- Work from home
6d
Associate Brand Manager
Abbott Laboratories —Doncaster VIC
- Full-time
- Microsoft Office
- Communication skills
- Marketing
Discipline Lead, Nursing
RMIT University —Melbourne VIC
- $176,883 - $227,847 a year
- Full-time
- Management
- University
- Experience working with children
11d
Senior Manager, Strategic Projects
Murdoch Childrens Research Institute —Parkville VIC
- $124,071 - $144,745 a year
- Full-time
- No degree
- AI
- Communication skills
7d

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

CEBIS USA
Parkville VIC

Quick Apply

Job Details

Contract
13 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

associate medical science jobs in melbourne, vic

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

Clinical Research Associate

Analyst, Quality Control, Chemistry & Stability

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

Associate Scientist

Discipline Lead, Medical Radiations

(Fixed-Term) Manufacturing Associate

Senior / Clinical Research Associate

Associate Quality Assurance Filling x 2

Associate Data Scientist

Senior Clinical Research Associate - FSP Melbourne / Sydney

Test Analyst

Associate Territory Manager - Trauma

Senior Associate Quality Assurance Value Stream

Senior Manager / Assoc Director, Quality Assurance

Research Assistant - Physical Sciences

Associate Feasibility Director

Associate Brand Manager

Discipline Lead, Nursing

Senior Manager, Strategic Projects

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