In-Demand Clinical trials Jobs in Melbourne, Vic

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trials Program Manager
Monash University —St Kilda Road VIC
- $124,343 - $137,251 a year
- Full-time
- Hybrid work
- Management
- Negotiation
1d
Clinical Trials Coordinator
Ramsay Health Care —Heidelberg VIC
- Full-time
- Research
- Referral program
Quick Apply
Laboratory Assistant (18-Month Contract)
BioAgilytix —Melbourne VIC
- Contract
- Laboratory
- Management
- Laboratory experience
Quick Apply
4d
Clinical Trial Coordinator - 2 positions
St Vincent's Health Australia —Melbourne VIC
- $86,730 - $99,699 a year
- Full-time
- Bachelor's degree
12d
Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Clinical Sample Specialist - Biospecimen Operations
LabConnect, LLC —Port Melbourne VIC
- Full-time
- Microsoft Word
- Microsoft Excel
- Management
Quick Apply
Research Development Lead
COGNO —Melbourne VIC
- Full-time
- Hybrid work
- Research
Quick Apply
Research Nurse Coordinator
Austin Health —Melbourne VIC
- Part-time
- Organisational skills
- Communication skills
- Health insurance
6d
Site Enrolment & Engagement Lead
IQVIA —Melbourne VIC
- Full-time
- Bachelor's degree
- Recruiting
- Organisational skills
11d
Study Manager (Biology)
BioAgilytix —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
4d
Clinical Research Associate (Level I/II)
Thermo Fisher Scientific —Melbourne VIC
- Full-time
- Laboratory
- Patient monitoring
- Microsoft Office
- Parental leave
- Employee assistance program
Lead Pharmacist (Grade 4) - Advanced Therapies & Clinical Trials
Royal Children's Hospital —Melbourne VIC
- $127,535 - $148,309 a year
- Full-time
- Research
5d
Project Manager, Neuroscience Trials Australia (NTA)
The Florey Institute —Parkville VIC
- Full-time
- Microsoft Office
- Bachelor's degree
- Organisational skills
6d
Scientist (Flow)
BioAgilytix —Melbourne VIC
- Full-time
- Management
- Doctoral degree
- Writing skills
Quick Apply
14d
Research Fellow – Tissue Acquisition & Biobanking
Cabrini Health —Malvern VIC
- Up to $18,850 a year
- Full-time
- Management
- Research
- Bachelor's degree
- Commuter assistance
12d
Clinical Trial Assistant - Phlebotomy/Laboratory
Cabrini Health —Malvern VIC
- Full-time
- Blood sampling
- Vital signs
- Commuter assistance
12d
Research Nurse
Murdoch Childrens Research Institute —Parkville VIC
- $96,365 - $105,325 a year
- Part-time
- Nursing
- Blood sampling
- Bachelor's degree
- Employee assistance program
5d
Scientist Grade 1 – Molecular Pathology Wetlab
Peter MacCallum Cancer Centre —Parkville VIC
- $63,674.00 - $91,785.20 a year
- Full-time
- Laboratory
- Customer service
- Laboratory experience
- Annual leave
5d
Analyst (PBMC)
BioAgilytix —Melbourne VIC
- Full-time
- Laboratory
- Management
- Writing skills
Quick Apply
4d

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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.

Apply Now

Refine Your Search

clinical trials jobs in melbourne, vic

Senior / Clinical Research Associate

Clinical Trials Program Manager

Clinical Trials Coordinator

Laboratory Assistant (18-Month Contract)

Clinical Trial Coordinator - 2 positions

Clinical Research Associate

Clinical Sample Specialist - Biospecimen Operations

Research Development Lead

Research Nurse Coordinator

Site Enrolment & Engagement Lead

Study Manager (Biology)

Clinical Research Associate (Level I/II)

Lead Pharmacist (Grade 4) - Advanced Therapies & Clinical Trials

Project Manager, Neuroscience Trials Australia (NTA)

Scientist (Flow)

Research Fellow – Tissue Acquisition & Biobanking

Clinical Trial Assistant - Phlebotomy/Laboratory

Research Nurse

Scientist Grade 1 – Molecular Pathology Wetlab

Analyst (PBMC)

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