In-Demand Research assistant Jobs

Senior / Clinical Research Associate
IQVIA —North Sydney NSW
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Research Associate
IQVIA —Sydney NSW
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Clinical Trial Assistant (1 Year Contract)
IQVIA —North Sydney NSW
- Contract
- Administrative experience
Graduate Research Coordinator
University of Melbourne —Parkville VIC
- $7 - $120,453 a year
- Full-time
- Research
- Microsoft Office
- Administrative experience
- Health insurance
- Parental leave
3d
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
5d
Assistant Accountant, Research
Deakin University —Waurn Ponds VIC
- $100,128 - $108,130 a year
- Full-time
- Hybrid work
- Finance
- Analysis skills
- University
- Parental leave
- Employee discount
2d
Trainee Research Technician – FILLED BY US!
National Agri-Solutions —New South Wales
- Full-time
- Management
- Research
- Communication skills
Clinical Research Associate
Orygen, The National Centre of Excellence in Youth Mental Health —Parkville VIC
- $125,000 - $135,000 a year
- Full-time
- Hybrid work
- Management
- Research
- Bachelor's degree
2d
Research Analyst - Property Economics Student or Recent Graduate
Cushman & Wakefield —Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
4d
Research and Development Laboratory Technician - CFT
Wagners —Toowoomba QLD
- Full-time
- Laboratory
- Laboratory experience
- Forklift
5d
Associate Director, Research Analytics
University of Canberra —Bruce SA
- $145,115 - $150,142 a year
- Full-time
- Research
- Leadership
- Health insurance
- Employee assistance program
6d
Clinical Trials and IP Officer
SA Health —Adelaide SA
- $92,122 - $102,456 a year
- Full-time
- Research
- No degree
- Leadership
- Annual leave
- Employee assistance program
2d
Research Associate, Sydney
Perrett Laver Internal —Sydney NSW
- Hybrid work
- In-person
- Leadership
4d
Clinical Trials Coordinator- Cardiology Research
Barwon Health —Geelong VIC
- Temporary
- Patient monitoring
- Research
- Microsoft Office
- Employee assistance program
Senior Clinical Research Officer - Clinical Trials
NSW Health —Wollongong NSW
- $114,251 - $134,809 a year
- Full-time
- Research
- Employee assistance program
- Gym membership
11d
Senior Clinical Research Officer - Clinical Trials
Illawarra Shoalhaven Local Health District —Wollongong NSW
- $114,251 - $134,809 a year
- Full-time
- Research
- Employee assistance program
- Gym membership
11d
Physiotherapist - Advanced Research Coordinator
Queensland Government —Brisbane QLD
- Temporary
- Research
- Travel reimbursement
- Parental leave
13d
Research Associate in Child and Adolescent Mental Health
Flinders University —Bedford Park SA
- $90,930 - $110,197 a year
- Full-time
- Doctoral degree
- Research
- Supervising experience
10d
Senior Clinical Research Associate - CNS/Early Phase - Australia - Remote
Worldwide Clinical Trials —Remote
- Full-time
- Nursing
- Microsoft Office
- Bachelor's degree
Associate Professor (Research), Australian Centre for AI in Medical Innovation
La Trobe University —Bundoora VIC
- From $172,864 a year
- Full-time
- Doctoral degree
- Working with children
- Recruiting
9d

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Senior / Clinical Research Associate

IQVIA -
North Sydney NSW

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Job Details

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Patient monitoring
Bachelor's degree
Computer skills
Financial management
Communication skills

Full Job Description

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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