In-Demand Research associate Jobs

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
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Associate Research Fellow
Deakin University —Waurn Ponds VIC
- $86,599 - $116,417 a year
- Part-time
- Hybrid work
- Doctoral degree
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- Parental leave
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Clinical Research Associate (Level I/II)
Thermo Fisher Scientific —Almaden QLD
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- Laboratory
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- Parental leave
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Clinical Research Associate
ICON Plc —Sydney NSW
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Clinical Research Associate II - Sydney
Fortrea —Sydney NSW
- Full-time
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Quality Assurance Associate
Queensland Government —Brisbane QLD
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- Negotiation
Associate/Graduate role
Right Lane Consulting Pty Ltd —Melbourne VIC
- Full-time
- Hybrid work
- Bachelor's degree
- Communication skills
Quick Apply
Travel Advisor - Remote Team
Travel Associates —Canberra ACT
- $110,000 a year
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Field Research Associate - Adelaide
Domain Group —Greater Adelaide SA
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2d
Associate Dean (Research Education)
University of Sydney —Darlington WA
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Associate Research Fellow
University of Wollongong —Sydney NSW
- $97,061 - $113,715 a year
- Full-time
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Social Impact Consultant
Worley —Melbourne VIC
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Field Research Associate - Perth
Domain Group —Perth WA
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2d
Associate Environmental Scientist/Engineer
Onterris —Greater Adelaide SA
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Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
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- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Advanced Associate, Content Researcher
Pearson —Melbourne VIC
- Full-time
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Literary Agent and Artist Manager
Aurora Artists' Management —Newtown NSW
- Full-time
- Microsoft Word
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Quick Apply
9d
Research Associate
Curtin University of Technology —Perth WA
- $104,917 - $112,487 a year
- Full-time
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1d
Associate Environmental Scientist/Engineer
Environmental Standards, Inc. —Greater Adelaide SA
- Full-time
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

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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

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