In-Demand Audit associate Jobs in North Ryde, Nsw

Start-up Associate (Clinical Trial Associate) - Sydney
Fortrea —Sydney NSW
- Full-time
- Office
- Bachelor's degree
9d
Associate - Fund Management
Macquarie Group Limited —Sydney NSW
- Full-time
- Hybrid work
- Organisational skills
- Financial services
- Communication skills
- Annual leave
- Work from home
4d
Country Regulatory Compliance Officer - Associate
JPMorganChase —Sydney NSW
- Full-time
- Organisational skills
- Financial services
- Communication skills
Community Associate, Sydney
WeWork —Sydney NSW
- Full-time
- Hospitality
- Bar
- Sales
12d
Clinical Research Associate I (FSP)
Thermo Fisher Scientific —Sydney NSW
- Full-time
- Laboratory
- Patient monitoring
- Education
- Parental leave
- Employee assistance program
5h
Clinical Research Associate II
AbbVie —Sydney NSW
- Full-time
- Remote
- Patient monitoring
- Bachelor's degree
- Organisational skills
5d
Consignment Co-ordinator
Alcon —Macquarie Park NSW
- Full-time
- Microsoft Excel
- Administrative experience
- Analysis skills
3d
Insurance External Auditor | Senior Associate | Financial Services
PWC Australia —Sydney NSW
- Parental leave
Site Supervisor (Building Associate)
CLMU Pty Ltd —Sydney Western Suburbs NSW
- $100,000 - $120,000 a year
- Full-time
- Construction site
- In-person
- Associate degree
Quick Apply
Analyst/Associate — Equity Research (TMT), Australia
JPMorganChase —Sydney NSW
- Full-time
- Research
- Communication skills
Senior Associate, Operational Risk (B&PB Value Chain)
ANZ Banking Group —Sydney NSW
- Full-time
- Analysis skills
- Communication skills
22h
Associate — Global Valuations & Portfolio Analytics
Macquarie Group Limited —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Excel
- Annual leave
- Work from home
Transaction Services FDD Specialist | Associate Director | Deals
PWC Australia —Sydney NSW
- Finance
- Master's degree
- Analysis skills
- Parental leave
Corporate EHS Manager, ANZ, Global Corporate Environmental, Health, Safety & Impact (EHSI)
Amazon Support Services Pty Ltd —Sydney NSW
- Full-time
- Management
- Microsoft Office
- Master's degree
1d
Sr Clinical Research Associate I Sydney, Melbourne, or Perth
Fortrea —Sydney NSW
- Full-time
- Management
- Patient monitoring
- Administrative experience
Senior Associate - External Manufacturing Quality
Reckitt —Sydney NSW
- Bachelor's degree
- Manufacturing
- Communication skills
- Employee assistance program
- Life insurance
12d
Accountant
Hamdan & Associates —Rockdale NSW
- $79,000 - $82,000 a year
- Full-time
- Analysis skills
- Education
- Bachelor's degree
- Parental leave
- Professional development assistance
Quick Apply
8d
Senior Clinical Research Associate
Thermo Fisher Scientific —Sydney NSW
- Full-time
- Laboratory
- Patient monitoring
- Research
- Relocation assistance
- Parental leave
Operations Supervisor
Amazon Commercial Services Pty Ltd —Moorebank NSW
- Overtime
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Health and Safety Associate Manager
Accenture —Sydney NSW
- Full-time
- Analysis skills
- Employee assistance program

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Start-up Associate (Clinical Trial Associate) - Sydney

Fortrea -
Sydney NSW

Apply Now

Job Details

Full-time
9 days ago

Qualifications

Bachelor's degree
Clinical trials

Full Job Description

Job Overview:

Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site Readiness team. Develop awareness of regulatory legislation, guidance, and practice in the assigned countries with the support from senior staff.

Summary of Responsibilities:

Develop awareness of regulatory legislation, guidance, and practice in the assigned countries with the support from senior staff.
Assist senior staff to compile, prepare, submit, and obtain approval of the submission documents to IRB/IEC/Third body/Regulatory Authority in accordance with local requirements.
Liaise with internal and external vendors in the generation of Regulatory Authority submissions (as applicable).
Perform a review of final submission documents as applicable.
Organize communication related to the submissions/outcomes within Fortrea as applicable.
Escalate study issues appropriately and in a timely fashion.
Perform other duties as assigned by management depending upon country and situational requirements with proper supervision (if applicable).

In Country specific tasks (Global):

Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.
Collect and track all the necessary documents required and perform a quality review, formatting, and compilation of the final documents for effective and compliant site activation and maintenance.
Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines.
Update study documents when there are changes in study personnel/study amendments.
Ensure high quality documents are filed and systems are updated on an ongoing and timely basis, making Fortrea ready for an audit at any time.
Update status reports, applicable logs, and tracking systems as applicable for the projects with input provided by senior staff.
With guidance from line manager and experienced colleagues, adapt Informed Consent Forms and other patient facing material to country specific requirements.
May support / assist the contract negotiation process under supervision of an experienced colleague or line manager.
Proactively identifying and escalating to Submission Leads any risk to meeting deliverables.
Notify the Submissions Lead of hours identified as Out-of-Scope or over burn with the support of more senior specialists.
All other duties as needed or assigned.

Qualifications (Minimum Required):

University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology).
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):

Minimum 0 – 2 + years of experience, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
Working knowledge of ICH, RA, IRB/IEC, and other applicable regulations/guidelines
Demonstrated basic understanding of the clinical trial process.

Physical Demands/Work Environment:

General Office Environment.

Learn more about our EEO & Accommodations request here .

Apply Now

Refine Your Search

audit associate jobs in north ryde, nsw

Start-up Associate (Clinical Trial Associate) - Sydney

Associate - Fund Management

Country Regulatory Compliance Officer - Associate

Community Associate, Sydney

Clinical Research Associate I (FSP)

Clinical Research Associate II

Consignment Co-ordinator

Insurance External Auditor | Senior Associate | Financial Services

Site Supervisor (Building Associate)

Analyst/Associate — Equity Research (TMT), Australia

Senior Associate, Operational Risk (B&PB Value Chain)

Associate — Global Valuations & Portfolio Analytics

Transaction Services FDD Specialist | Associate Director | Deals

Corporate EHS Manager, ANZ, Global Corporate Environmental, Health, Safety & Impact (EHSI)

Sr Clinical Research Associate I Sydney, Melbourne, or Perth

Senior Associate - External Manufacturing Quality

Accountant

Senior Clinical Research Associate

Operations Supervisor

Health and Safety Associate Manager

I want to receive the latest job alert for audit associate in north ryde, nsw

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