In-Demand Clinical trials Jobs in Melbourne, Vic

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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
4d
Clinical Trials Project Coordinator
Australian Catholic University —Melbourne VIC
- $105,212 - $113,823 a year
- Full-time
- Hybrid work
- University
2d
Clinical Research Associate II - Sydney, Melbourne or Adelaide
Fortrea —Melbourne VIC
- Full-time
- Patient monitoring
- Bachelor's degree
Clinical Trials Coordinator | Endoscopy
St Vincent's Health Australia —Melbourne VIC
- $128,102 a year
- Full-time
- Nursing
- Research
- Bachelor's degree
3d
Clinical Trial Coordinator
The Royal Melbourne Hospital —Parkville VIC
- Full-time
- Patient monitoring
- Microsoft Office
- Communication skills
Clinical Research Associate
IQVIA —Melbourne VIC
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Clinical Trial Quality Officer
University of Melbourne —Parkville VIC
- $111,275 - $120,453 a year
- Full-time
- Research
- Health insurance
- Parental leave
Clinical Research Coordinator (Nurse)
Monash Health —Clayton VIC
- Full-time
- Research
- University
- Patient care
8d
Clinical Trial Materials Specialist I - Clinical Trial Materials
LabConnect, LLC —Port Melbourne VIC
- Full-time
- Microsoft Word
- Microsoft Excel
- Sales
Quick Apply
Study Coordinator
BioAgilytix —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
13h
Service Improvement Coordinator
Safer Care Victoria —Melbourne VIC
- $116,413 - $140,849 a year
- Part-time
- Writing skills
- Recruiting
- Editing
8d
ARC Research Fellow
Victoria University —Footscray VIC
- $113,221 - $134,499 a year
- Full-time
- Microsoft Excel
- Doctoral degree
- Research
Senior Laboratory Assistant
BioAgilytix —Melbourne VIC
- Full-time
- Laboratory
- Management
- Laboratory experience
Quick Apply
13h
Scientist (Molecular)
BioAgilytix —Melbourne VIC
- Full-time
- Management
- Doctoral degree
- Writing skills
Quick Apply
13h
Fellow - Clinical Research
St Vincent's Health Australia —Melbourne VIC
- $129,048.40 - $177,622.12 a year
- Part-time
- Patient care
- Communication skills
- Employee assistance program
Principal Scientist, Bioanalysis, Immunogenicity & Biomarkers
CSL Behring —Melbourne VIC
- Full-time
- Doctoral degree
- Research
- Master's degree
9d
Team Leader Wilson Blood Cancer Genomics – Molecular Pathology
Peter MacCallum Cancer Centre —Parkville VIC
- $127,535.20 - $148,309.20 a year
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Access
- Annual leave
1d
Site Enrollment and Engagement Lead - PAH/IPF
IQVIA —Melbourne VIC
- Contract
- Medicine
- Doctoral degree
- Bachelor's degree
10d
Associate Clinical Project Manager
IQVIA —Melbourne VIC
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel

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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 jobs in melbourne, vic

Senior / Clinical Research Associate

Study Coordinator - Clinical Trials

Clinical Trials Project Coordinator

Clinical Research Associate II - Sydney, Melbourne or Adelaide

Clinical Trials Coordinator | Endoscopy

Clinical Trial Coordinator

Clinical Research Associate

Clinical Trial Quality Officer

Clinical Research Coordinator (Nurse)

Clinical Trial Materials Specialist I - Clinical Trial Materials

Study Coordinator

Service Improvement Coordinator

ARC Research Fellow

Senior Laboratory Assistant

Scientist (Molecular)

Fellow - Clinical Research

Principal Scientist, Bioanalysis, Immunogenicity & Biomarkers

Team Leader Wilson Blood Cancer Genomics – Molecular Pathology

Site Enrollment and Engagement Lead - PAH/IPF

Associate Clinical Project Manager

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