In-Demand Clinical trials project manager Jobs in Melbourne Vic

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trials Project Manager
The Florey Institute —Parkville VIC
- Full-time
- Microsoft Office
- Bachelor's degree
- Organisational skills
10d
Study Coordinator - Clinical Trials
Peter MacCallum Cancer Centre —Parkville VIC
- $90,235.60 - $103,724.40 a year
- Part-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Access
- Annual leave
13d
Associate Clinical Project Manager
IQVIA —Melbourne VIC
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Research Associate
IQVIA —Melbourne VIC
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Project Manager - Clinical
PCI Pharma Services —Moorabbin VIC
- Overtime
- Remote
- Management
- Bachelor's degree
- Computer skills
- Work from home
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
1d
Cardiothoracic Research Manager
St Vincent's Health Australia —Melbourne VIC
- $127,535.20 - $137,696.00 a year
- Full-time
- Nursing
- Doctoral degree
- Master's degree
Clinical Trial Materials Specialist I - Clinical Trial Materials
LabConnect, LLC —Port Melbourne VIC
- Full-time
- Microsoft Word
- Microsoft Excel
- Sales
Quick Apply
Clinical Operation Consultant - ANZ
Veeva Systems —Melbourne VIC
- Full-time
- Computer Science
- Bachelor's degree
- SharePoint
Operations Director - Ambulatory Services
Peter MacCallum Cancer Centre —Parkville VIC
- Full-time
- Hybrid work
- Management
- Administrative experience
- Computer skills
- Annual leave
Manager, Site Start Up APAC
Precision Medicine Group —Melbourne VIC
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
2027 Oncology Clinical Trials Fellow
Monash Health —Clayton VIC
- Part-time
- Medicine
- Management
- University
Technical Implementation & Support Engineer (APAC)
Nicolab —Melbourne VIC
- $120,000 - $150,000 a year
- Part-time
- Remote
- AWS
- Education
- Bachelor's degree
- Annual leave
- Referral program
Quick Apply
Sr Manager, Medical Affairs
Gilead Sciences —Melbourne VIC
- Full-time
- Analysis skills
- Communication skills
Solution Specialist
IQVIA —Melbourne VIC
- Bachelor's degree
- Recruiting
- Communication skills
Senior Laboratory Assistant
BioAgilytix —Melbourne VIC
- Full-time
- Laboratory
- Management
- Laboratory experience
Quick Apply
8d
Clinical Research Nurse
St Vincent's Health Australia —Melbourne VIC
- $134,498 - $137,696 a year
- Full-time
- Nursing
- Bachelor's degree
- Computer skills
Pharmacist Grade 2 – Aseptic Manufacturing
Peter MacCallum Cancer Centre —Parkville VIC
- Up to $106,907 a year
- Part-time
- Management
- Manufacturing
- Communication skills
- Annual leave
Senior Lawyer (Research & Education)
Monash University —Clayton VIC
- $145,062 - $153,976 a year
- Full-time
- Hybrid work
- Communication skills
- Office experience
5d

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Senior / Clinical Research Associate

IQVIA -
Melbourne VIC

Apply Now

Job Details

Qualifications

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

Full Job Description

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.

Apply Now

Refine Your Search

clinical trials project manager jobs in melbourne vic

Senior / Clinical Research Associate

Clinical Trials Project Manager

Study Coordinator - Clinical Trials

Associate Clinical Project Manager

Clinical Research Associate

Project Manager - Clinical

Research Administrative Officer

Cardiothoracic Research Manager

Clinical Trial Materials Specialist I - Clinical Trial Materials

Clinical Operation Consultant - ANZ

Operations Director - Ambulatory Services

Manager, Site Start Up APAC

2027 Oncology Clinical Trials Fellow

Technical Implementation & Support Engineer (APAC)

Sr Manager, Medical Affairs

Solution Specialist

Senior Laboratory Assistant

Clinical Research Nurse

Pharmacist Grade 2 – Aseptic Manufacturing

Senior Lawyer (Research & Education)

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