In-Demand Clinical associate Jobs in Australia

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Associate
Globus Medical —Brisbane QLD
- Full-time
- Hospital experience
Clinical Research Associate
Northern Sydney Local Health District —Sydney NSW
- $87,813 - $116,824 a year
- Full-time
- Management
- No degree
- Hospital experience
12d
Clinical Research Associate II - Sydney
Fortrea —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
Clinical Research Associate
NSW Health —St Leonards NSW
- $1,682.93 - $2,238.93 a week
- Temporary
- Management
- No degree
- Hospital experience
12d
Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane
Thermo Fisher Scientific —Brisbane QLD
- Full-time
- Remote
- Nursing
- Patient monitoring
- Microsoft Office
- Travel reimbursement
- Parental leave
Clinical Site Associate / Clinical Trial Associate
ICON Plc —Sydney NSW
- Full-time
- Microsoft Office
- Administrative experience
- Bachelor's degree
- Health insurance
- Dental insurance
3d
Associate Clinical Educator - Nursing
University of the Sunshine Coast —Hervey Bay QLD
- $83,148 - $112,588 a year
- Full-time
- Nursing
- Employee assistance program
Clinical Research Associate (I) and (II)
Novo Nordisk —Sydney NSW
- Patient monitoring
- Clinic
- Bachelor's degree
Clinical Operations Associate (Maternity Leave Cover)
Careers at Eucalyptus —New South Wales
- AI
- Annual leave
- Parental leave
Clinical Research Associate (Contractor) Australia
Allucent —Melbourne VIC
- Part-time
- Patient monitoring
Quick Apply
Clinical Research Associate
ICON Plc —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
- Communication skills
- Health insurance
- Dental insurance
Executive Assistant To Associate Director Clinical Operations
NSW Health —Lismore NSW
- Part-time
- AI
- Travel reimbursement
1d
Clinical Trials Administrator (Start-Up Associate)
University of the Sunshine Coast —Buderim QLD
- $82,843 - $93,358 a year
- Full-time
- Employee assistance program
14d
Clinical Research Associate (Level I/II)
Thermo Fisher Scientific —Sydney NSW
- Full-time
- Laboratory
- Patient monitoring
- Microsoft Office
- Parental leave
- Employee assistance program
Quality Assurance Associate
Queensland Government —Brisbane QLD
- Part-time
- Negotiation
5d
Associate Director Virtual Clinical Care Centre
NSW Health —Sydney Olympic Park NSW
- $175,250 - $209,681 a year
- Full-time
- Remote
- AI
- Leadership
- Negotiation
- Travel reimbursement
14d
Associate Clinical Nurse Consultant
Queensland Government —Brisbane QLD
- Part-time
- Nursing
3d
Sr Pharmacovigilance Associate
Novo Nordisk —Sydney NSW
14d
Clinical Research Associate
IQVIA —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance

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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 associate jobs in australia

Senior / Clinical Research Associate

Clinical Associate

Clinical Research Associate

Clinical Research Associate II - Sydney

Clinical Research Associate

Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane

Clinical Site Associate / Clinical Trial Associate

Associate Clinical Educator - Nursing

Clinical Research Associate (I) and (II)

Clinical Operations Associate (Maternity Leave Cover)

Clinical Research Associate (Contractor) Australia

Clinical Research Associate

Executive Assistant To Associate Director Clinical Operations

Clinical Trials Administrator (Start-Up Associate)

Clinical Research Associate (Level I/II)

Quality Assurance Associate

Associate Director Virtual Clinical Care Centre

Associate Clinical Nurse Consultant

Sr Pharmacovigilance Associate

Clinical Research Associate

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