In-Demand Clinical research Jobs in Hobart, Tas

Clinical Research Coordinator - Hobart TAS
IQVIA —Hobart TAS
- Urgently hiring
- Microsoft Word
- Microsoft Excel
- Microsoft Access
Site Enrollment and Engagement Lead (1 Year Contract)
IQVIA —Hobart TAS
- Full-time
- Medicine
- Doctoral degree
- Office
Part Time Medical Administrator
Icon Group —Hobart TAS
- Part-time
- Microsoft Outlook
- Customer service
- Administrative experience
- Parental leave
- Employee assistance program
8d
Principal Consultant - Registered or Clinical Psychologist
Altius Group —Hobart TAS
- Full-time
- Master's degree
- Leadership
- Parental leave
- Employee assistance program
Quick Apply
Clinical Provider (Hobart, TAS - Australia)
Intellect —Hobart TAS
- Contract
- Remote
- Private practice
- Master's degree
- Psychology
- Employee assistance program
Quick Apply
Registered Psychologist
Altius Group —Hobart TAS
- Full-time
- Parental leave
- Employee assistance program
Quick Apply

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Site Enrollment and Engagement Lead (1 Year Contract)
IQVIA —Hobart TAS
In some studies, interacting directly with patients to provide education on the trial, disease area, or device/medication (where required and appropriate).

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Clinical Research Coordinator - Hobart TAS

IQVIA -
Hobart TAS

Apply Now

Job Details

Full-time

Qualifications

Microsoft Word
Microsoft Excel
Microsoft Access
Vital signs
Microsoft Outlook
English
Microsoft Office
Education
Bachelor's degree
Organisational skills
Clinical trials
IT
Medical terminology
Communication skills
Information Technology

Full Job Description

Hobart, Australia | Full time | Field-based | R1562353

Clinical Research Coordinator or Clinical Research Nurse in Hobart TAS

Working Hours: 24 hours per week

Start Date: Immediately
Duration: Approximately 6 months

IQVIA is currently recruiting a dedicated Clinical Research Coordinator or Clinical Research Nurse to support a clinical research site in Hobart TAS. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

Key Responsibilities

As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:

Prescreening and Screening tasks
Review charts from the site data base
Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
Supporting patient screening and enrollment, including handling informed consent and privacy documentation
Coordinating logistical activities for study procedures in line with the study protocol
Processing lab samples
Attend patient visits including ECG, vitals and potentially blood draws
Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
Patient education
Communicating with study monitors and responding to study-related inquiries
Carrying out general administrative tasks related to the study

Your Profile
We are looking for candidates who bring a combination of education, experience, and skills:

Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
Good knowledge of medical terminology
Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
Excellent interpersonal and communication skills
Strong organizational skills and attention to detail
Fluency in English

Why Join IQVIA?
At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.

Interested?
If this sounds like the right opportunity for you, we encourage you to apply today.

#LI-HCPN

#LI-CES

#LI-DNP

#LI-CT1

#LI-Onsite

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

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

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

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clinical research jobs in hobart, tas

Clinical Research Coordinator - Hobart TAS

Site Enrollment and Engagement Lead (1 Year Contract)

Part Time Medical Administrator

Principal Consultant - Registered or Clinical Psychologist

Clinical Provider (Hobart, TAS - Australia)

Registered Psychologist

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