In-Demand Clinical trial Jobs in Mill Park Vic

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trials Assistant - Radiation Oncology
Peter MacCallum Cancer Centre —Parkville VIC
- $60,780 - $67,194 a year
- Full-time
- Hybrid work
- Patient monitoring
- Clinic
- Data entry
- Annual leave
7d
Clinical Research Associate
Orygen, The National Centre of Excellence in Youth Mental Health —Parkville VIC
- $125,000 - $135,000 a year
- Full-time
- Hybrid work
- Management
- Research
- Bachelor's degree
13d
Medical Laboratory Technician Grade 1 - Anatomical Pathology
Peter MacCallum Cancer Centre —Parkville VIC
- Up to $11,660 a year
- Full-time
- Laboratory
- Laboratory experience
- Associate degree
7d
Med Lab Tech Gr 1
St Vincent's Health Australia —Melbourne VIC
- $59,207 - $76,346 a year
- Full-time
- Laboratory experience
- Maintenance
- No degree
Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Research Fellow, Australian Centre for AI in Medical Innovation
La Trobe University —Bundoora VIC
- From $118,530 a year
- Full-time
- Doctoral degree
- Research
- Experience working with children
Clinical Research Coordinator (FISS-Australia Project)
La Trobe University —Bundoora VIC
- $106,472 - $117,127 a year
- Part-time
- Research
- University
- Experience working with children
7d
Research Administrative Officer
Monash University —St Kilda Road VIC
- $86,344 - $99,179 a year
- Full-time
- Hybrid work
- Customer service
- Microsoft Office
- Administrative experience
13d
Medical Laboratory Technician Grade 1 - Molecular Pathology
Peter MacCallum Cancer Centre —Parkville VIC
- $59,207.20 - $76,346.40 a year
- Full-time
- Laboratory
- Laboratory experience
- Education
- Annual leave
7d
Quality Assurance Assistant
Cencora —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
3d
PhD Scholarships – optimising blood product use in Australia
Monash University —St Kilda Road VIC
- Up to $46,000 a year
- Part-time
- Doctoral degree
- Research
- University
Female Support Worker (clients choice): MND + Complex care Experience: Balwyn + Box Hill Areas
Absolute in Home Care —Balwyn VIC
- $34 - $45 an hour
- Patient monitoring
- In-person
- Travel reimbursement
- Employee discount
Quick Apply
Clinical Trials Project Manager
Peter MacCallum Cancer Centre —Parkville VIC
- $96,570.76 - $106,759.12 a year
- Part-time
- Hybrid work
- Research
- Clinic
- Budgeting
- Annual leave
9d
Associate Professor (Research), Australian Centre for AI in Medical Innovation
La Trobe University —Bundoora VIC
- From $172,864 a year
- Full-time
- Doctoral degree
- Experience working with children
- Recruiting
Senior Research Fellow, Australian Centre for AI in Medical Innovation
La Trobe University —Bundoora VIC
- From $144,266 a year
- Full-time
- Doctoral degree
- Research
- Experience working with children
Manager, Research Strategy and Clinical Trials
Safer Care Victoria —Melbourne VIC
- $142,790 - $191,084 a year
- Full-time
- Research
- Master's degree
- Recruiting
13d
Clinical Specialist - TAVR - AU
Anteris Technologies —Melbourne VIC
- $145,000 - $200,000 a year
- Remote
- Nursing
- Anatomy knowledge
- Bachelor's degree
- Annual leave
Quick Apply
8d
Senior Laboratory Assistant
BioAgilytix —Melbourne VIC
- Full-time
- Laboratory
- Management
- Laboratory experience
Quick Apply
Pharmacy Technician Grade 1
Cabrini Health —Malvern VIC
- Full-time
- Customer service
- Computer skills
- Communication skills
- Commuter assistance
- On-the-job training

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Senior / Clinical Research Associate

IQVIA -
Melbourne VIC

Apply Now

Job Details

Full-time

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Patient monitoring
Bachelor's degree
Computer skills
Financial management
Communication skills

Full Job Description

Melbourne, Australia | Full time | Hybrid | R1525252

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree in scientific discipline or health care.
Requires at least 1 year of on-site monitoring experience.
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Candidates will be assessed according to their years of experience and be considered for various levels where applicable.

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

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

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

clinical trial jobs in mill park vic

Senior / Clinical Research Associate

Clinical Trials Assistant - Radiation Oncology

Clinical Research Associate

Medical Laboratory Technician Grade 1 - Anatomical Pathology

Med Lab Tech Gr 1

Clinical Research Associate

Research Fellow, Australian Centre for AI in Medical Innovation

Clinical Research Coordinator (FISS-Australia Project)

Research Administrative Officer

Medical Laboratory Technician Grade 1 - Molecular Pathology

Quality Assurance Assistant

PhD Scholarships – optimising blood product use in Australia

Female Support Worker (clients choice): MND + Complex care Experience: Balwyn + Box Hill Areas

Clinical Trials Project Manager

Associate Professor (Research), Australian Centre for AI in Medical Innovation

Senior Research Fellow, Australian Centre for AI in Medical Innovation

Manager, Research Strategy and Clinical Trials

Clinical Specialist - TAVR - AU

Senior Laboratory Assistant

Pharmacy Technician Grade 1

I want to receive the latest job alert for clinical trial in mill park vic

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