In-Demand Research assistant Jobs in Epping Vic

Clinical Independent Rater for Clinical Trial - Mandarin Speaking
IQVIA —Melbourne VIC
- Part-time
- Remote
- Medicine
- Doctoral degree
- English
- Work from home
5d
Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trial Manager (FSP)
Thermo Fisher Scientific —Melbourne VIC
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Parental leave
- Employee assistance program
4d
Senior Clinical Research Associate - FSP Melbourne / Sydney
Fortrea —Melbourne VIC
- Full-time
- Management
- Patient monitoring
- Administrative experience
Associate Director Research Finance
University of Melbourne —Parkville VIC
- Full-time
- Research
- Finance
- Analysis skills
- Health insurance
- Parental leave
10d
Clinical Trials Research Nurse - Level 2
Peter MacCallum Cancer Centre —Parkville VIC
- Up to $115,289.20 a year
- Full-time
- Patient monitoring
- Research
- Education
- Annual leave
Research Nurse Level 3 - Clinical Trials
Peter MacCallum Cancer Centre —Parkville VIC
- $11,660 - $128,102 a year
- Full-time
- Hybrid work
- Laboratory
- Research
- Education
- Annual leave
11d

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Clinical Independent Rater for Clinical Trial - Mandarin Speaking

IQVIA -
Melbourne VIC

Apply Now

Job Details

Part-time
5 days ago

Benefits

Work from home

Qualifications

Mandarin
Medicine
Doctoral degree
English
Research
Microsoft Office
Master's degree
Education
Psychology
Organisational skills
Communication skills
Time management

Full Job Description

Melbourne, Australia | Part time | Home-based | R1564216

Clinical Independent Rater - Mandarin Speaking

Location: Remote/Virtual
Hours: Estimated 10–16 hours per month
Role: Clinical Specialist

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

Position Overview

The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation.

Key Responsibilities

Participate in all required orientation, training, and calibration activities.
Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.
Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.
Complete assigned tasks and rater interactions according to schedule.
Submit all required documentation accurately and on time.

Required Qualifications

Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
Experience:
- Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically MINI and MADRS).
- Minimum 3 years of clinical experience with psychiatric populations.
- Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).
- Experience in CNS trials preferred.
Skills:
- Strong interpersonal and communication skills for professional interaction at all levels.
- Excellent organizational skills, attention to detail, time management, and problem-solving ability.
- Proficiency with Windows and Microsoft Office applications.

Language Requirement

Current openings require fluency in English and native-level proficiency in Mandarin.

#LI-DNP #LI-Remote #LI-HCPN

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

research assistant jobs in epping vic

Clinical Independent Rater for Clinical Trial - Mandarin Speaking

Senior / Clinical Research Associate

Clinical Trial Manager (FSP)

Senior Clinical Research Associate - FSP Melbourne / Sydney

Associate Director Research Finance

Clinical Trials Research Nurse - Level 2

Research Nurse Level 3 - Clinical Trials

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