In-Demand healthcare data science Jobs in melbourne vic

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trial Coordinator - 2 positions
St Vincent's Health Australia —Melbourne VIC
- $86,730 - $99,699 a year
- Full-time
- Bachelor's degree
14h
Clinical Trials Assistant 1 (1 Year Contract, Sponsor Dedicated)
IQVIA —Melbourne VIC
- Full-time
- Administrative experience
2h
Clinical Data Engineer
Murdoch Childrens Research Institute —Parkville VIC
- $110,279 - $134,292 a year
- Full-time
- Computer science
- SQL
- AI
- Commuter assistance
- Parental leave
Microbiological Analyst QC
BioNTech AG —Melbourne VIC
- Full-time
- Bachelor's degree
- Communication skills
Medical Science Liaison – Oncology Pipeline (VIC / SA)
GlaxoSmithKline —Melbourne VIC
- Full-time
- Medicine
- Doctoral degree
- Master's degree
- Annual leave
Analyst, Quality Control, Chemistry & Stability
Moderna, Inc. —Melbourne VIC
- Full-time
- Laboratory
- Bachelor's degree
- In-person
- Annual leave
CHSRC Data Analyst
Peter MacCallum Cancer Centre —Parkville VIC
- $74,448.40 - $93,003.00 a year
- Full-time
- Hybrid work
- Research
- Administrative experience
- SQL
- Annual leave
2d
Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Regulatory Affairs & Quality Specialist
Steris —Melbourne VIC
- Full-time
- English
- Microsoft Office
- SharePoint
Research Scientist, BCI-Australia
Synchron Inc. —Melbourne VIC
- $100,000 - $220,000 a year
- Full-time
- Remote
- Doctoral degree
- Computer Science
- Research
- Commuter assistance
- Health insurance
Quick Apply
Quality Assurance for Quality Control, Australia
Moderna, Inc. —Melbourne VIC
- Full-time
- Management
- Education
- Bachelor's degree
- Annual leave
Regulatory and Site Start Up Specialist
Precision for Medicine —Melbourne VIC
- Remote
- Medicine
- Doctoral degree
- English
Quick Apply
Clinical Support Specialist
For Health Group —Richmond VIC
- Full-time
- Remote
- Customer service
- Microsoft Office
- Computer skills
- Work from home
9d
Pharma Specialist Rep (PJP) - Immuno/Nephro - VIC/TAS/SA - 12 Months Max Term Contract
Roche —Melbourne VIC
- Contract
- Bachelor's degree
- No degree
- Business
12d
Analyst, Channel Dynamics
IQVIA —Melbourne VIC
- Full-time
- Hybrid work
- Analysis skills
- Bachelor's degree
- Organisational skills
- On-the-job training
3d
Quality & Compliance Manager
Downer Group —Melbourne VIC
- Management
- Employee assistance program
Manager, Global Clinical Monitoring (CRA Line Manager)
Precision Medicine Group —Melbourne VIC
- Remote
- Patient monitoring
- Supervising experience
- Bachelor's degree
10d
Clinical Trials Coordinator
Ramsay Health Care —Heidelberg VIC
- Full-time
- Research
- Referral program
Quick Apply
Sales Specialist, Infusion Therapies & Platforms
Baxter —Brunswick VIC
- Management
- Sales
- Marketing
- Annual leave
6d

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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

healthcare data science jobs in melbourne vic

Senior / Clinical Research Associate

Clinical Trial Coordinator - 2 positions

Clinical Trials Assistant 1 (1 Year Contract, Sponsor Dedicated)

Clinical Data Engineer

Microbiological Analyst QC

Medical Science Liaison – Oncology Pipeline (VIC / SA)

Analyst, Quality Control, Chemistry & Stability

CHSRC Data Analyst

Clinical Research Associate

Regulatory Affairs & Quality Specialist

Research Scientist, BCI-Australia

Quality Assurance for Quality Control, Australia

Regulatory and Site Start Up Specialist

Clinical Support Specialist

Pharma Specialist Rep (PJP) - Immuno/Nephro - VIC/TAS/SA - 12 Months Max Term Contract

Analyst, Channel Dynamics

Quality & Compliance Manager

Manager, Global Clinical Monitoring (CRA Line Manager)

Clinical Trials Coordinator

Sales Specialist, Infusion Therapies & Platforms

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