In-Demand Science & research Jobs in The Rocks, Nsw

Senior / Clinical Research Associate
IQVIA —North Sydney NSW
- Full-time
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Sleep Technician
Meredith Respiratory and Sleep Centre —Bankstown NSW
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Other Spatial Scientist
AI Talent —Sydney NSW
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1d
Clinical Data Associate
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Medical Affairs (Field MSL) - Neuro - NSW/QLD
Roche —Sydney NSW
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Clinical Trial Assistant (1 Year Contract)
IQVIA —North Sydney NSW
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Clinical AI Research Assistant
Insight Timer —Sydney NSW
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11d
Trust Board Member + Chair
Crown Lands and Public Spaces —Sydney NSW
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Metallurgist
AI Talent —Sydney NSW
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12d
Co-Founder
Sofodel —Sydney NSW
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Clinical Site Associate / Clinical Trial Associate
ICON Plc —Sydney NSW
- Full-time
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Lead Archivist Institutional Archives
Museum of Applied Arts and Sciences —Sydney NSW
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Clinical Research Associate (Level I/II)
Thermo Fisher Scientific —Sydney NSW
- Full-time
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Clinical Research Coordinator - Blacktown
IQVIA —North Sydney NSW
- Part-time
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Clinical Research Associate (I) and (II)
Novo Nordisk —Sydney NSW
- Patient monitoring
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Research Genetic Counsellor
The Garvan Institute of Medical Research —Sydney NSW
- $85,000 a year
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Research Assistant
University of Sydney —Camperdown NSW
- $83,038 - $89,755 a year
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- Computer Science
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3d
Clinical Research Coordinator
GenesisCare —St Leonards NSW
- Full-time
- Nursing
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Trainee - Unaccredited Position
NSW Health —St Leonards NSW
- Part-time
- Research
- Communication skills
- Time management
13d
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 -
North Sydney NSW

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

Sydney North, 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

science & research jobs in the rocks, nsw

Senior / Clinical Research Associate

Sleep Technician

Other Spatial Scientist

Clinical Data Associate

Medical Affairs (Field MSL) - Neuro - NSW/QLD

Clinical Trial Assistant (1 Year Contract)

Clinical AI Research Assistant

Trust Board Member + Chair

Metallurgist

Co-Founder

Clinical Site Associate / Clinical Trial Associate

Lead Archivist Institutional Archives

Clinical Research Associate (Level I/II)

Clinical Research Coordinator - Blacktown

Clinical Research Associate (I) and (II)

Research Genetic Counsellor

Research Assistant

Clinical Research Coordinator

Trainee - Unaccredited Position

Clinical Research Associate

I want to receive the latest job alert for science & research in the rocks, nsw

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