In-Demand Clinical project manager Jobs in Carlton Vic

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Clinical Project Manager
IQVIA —Melbourne VIC
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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
6d
Head of Delivery
Bupa —Melbourne VIC
- Full-time
- Presentation skills
- Agile
- Leadership
9d
Project Manager - Clinical
PCI Pharma Services —Moorabbin VIC
- Overtime
- Remote
- Management
- Bachelor's degree
- Computer skills
- Work from home
Clinical Trials Project Manager
The Florey Institute —Parkville VIC
- Full-time
- Microsoft Office
- Bachelor's degree
- Organisational skills
Program Lead - Culturally Safe Partnerships
Peter MacCallum Cancer Centre —Melbourne VIC
- $87,003.80 - $96,181.00 a year
- Part-time
- Hybrid work
- Communication skills
- Annual leave
10d
HR Business Partner
Siemens Healthineers —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Office
- Human resources
- Analytics
- Employee assistance program
Manager, Supply Chain (Life Science / Healthcare)
Cencora —Melbourne VIC
- Full-time
- Hybrid work
- Writing skills
- Analysis skills
- Presentation skills
Community Fundraising Coordinator
Peter MacCallum Cancer Centre —Parkville VIC
- Up to $85,000 a year
- Full-time
- Hybrid work
- Management
- Databases
- Analysis skills
- Annual leave
6d
Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Senior Project Officer
Royal Children's Hospital —Melbourne Western Suburbs VIC
- $114,436.00 - $124,912.84 a year
- Part-time
- Paediatrics
- Employee assistance program
13d
People and Culture Business Partner
DPV Health —Melbourne VIC
- Full-time
- Leadership
- Communication skills
4d
Project Coordinator - Health Systems | 2 Year Contract
Movember —Melbourne VIC
- $76,000 - $85,000 a year
- Full-time
- Hybrid work
- Bar
- Microsoft Office
- Administrative experience
- Annual leave
- Parental leave
2h
Senior Laboratory Assistant
BioAgilytix —Melbourne VIC
- Full-time
- Laboratory
- Management
- Laboratory experience
Quick Apply
Group Manager Clinical Risk and National Standards
Epworth —Richmond VIC
- Full-time
- Data analysis skills
- Patient care
- Communication skills
Quick Apply
Adoption Specialist
Solventum —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Research Education Administrator
Peter MacCallum Cancer Centre —Parkville VIC
- $69,438 - $76,764 a year
- Full-time
- Hybrid work
- Doctoral degree
- Research
- Microsoft Office
- Annual leave
4d
Hospital Sales Representative - AIR - QLD
Chiesi Farmaceutici —Melbourne VIC
- Contract
- Nursing
- Doctoral degree
- Research
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
10d

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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 project manager jobs in carlton vic

Senior / Clinical Research Associate

Associate Clinical Project Manager

Clinical Trials Project Manager

Head of Delivery

Project Manager - Clinical

Clinical Trials Project Manager

Program Lead - Culturally Safe Partnerships

HR Business Partner

Manager, Supply Chain (Life Science / Healthcare)

Community Fundraising Coordinator

Clinical Research Associate

Senior Project Officer

People and Culture Business Partner

Project Coordinator - Health Systems | 2 Year Contract

Senior Laboratory Assistant

Group Manager Clinical Risk and National Standards

Adoption Specialist

Research Education Administrator

Hospital Sales Representative - AIR - QLD

Research Administrative Officer

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