In-Demand Clinical associate Jobs in Parramatta Nsw

Start-up Associate (Clinical Trial Associate) - Sydney
Fortrea —Sydney NSW
- Full-time
- Office
- Bachelor's degree
5d
Client Advocate Executive - HIS
Solventum —North Ryde NSW
- Full-time
- Bachelor's degree
- EMR systems
- Acute care experience
Senior Clinical Research Associate I (SCRA1) - Sydney, Melbourne, Adelaide or Brisbane
Fortrea —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
- No degree
- Opportunities for advancement
Regulatory and Study Start Up Clinical Trials
Chris O’Brien Lifehouse —Camperdown NSW
- Full-time
- Organisational skills
- Communication skills
- Negotiation
- Employee assistance program
5d
Senior Clinical Research Associate
PSI CRO —Sydney NSW
- Full-time
- Hybrid work
- Patient monitoring
- Microsoft Office
- Bachelor's degree
Quick Apply
5d
Global Study Management (Senior) Associate (Global CTA)
BeiGene —Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Patient monitoring
Psychologist / Rehabilitation Counsellor
Procare Group —Macquarie Park NSW
- Full-time
- Hybrid work
- Communication skills
- Parental leave
- Employee assistance program
4d
Data Engineer
Southern Cross Care (NSW & ACT) —Epping NSW
- Full-time
- Azure
- DevOps
- Engineering
- Employee assistance program
- Referral program
Quick Apply
Associate Sales Representative Sports Medicine - Newcastle
Arthrex —Sydney NSW
- Medicine
- Communication skills
- Time management
Postdoctoral Research Associate
University of Sydney —Camperdown NSW
- $117,936 - $157,381 a year
- Full-time
- Doctoral degree
- Research
- University
6d
Associate Territory Manager
Lexington Medical, Inc. —Sydney NSW
- On call
- Management
- Marketing
- Bachelor's degree
Quick Apply
5d
Associate Dentist North Rocks, New South Wales
Bupa —North Rocks NSW
4d
Territory Manager - Sydney South
Rayner Intraocular Lenses —Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
- Employee assistance program
1d
Product Specialist | BD Pyxis
BD —North Ryde NSW
- Nursing
- Sales
- Salesforce
5d
Territory Manager
Globus Medical —Sydney NSW
- Weekend availability
- Anatomy knowledge
- Management
- Sales
Speech Pathologist – All Levels (Senior, Associate, Graduate)
Healthproof —Parramatta NSW
- $80,000 - $125,000 a year
- Full-time
- Hybrid work
- Communication skills
- Work from home
- Referral program
Quick Apply
Life Sciences Cyber Intelligence Analyst
Accenture —Sydney NSW
- Full-time
- Bachelor's degree
- Associate degree
12d
Group Leader Immuno-Oncology
Children's Cancer Institute —Randwick NSW
- Full-time
- Doctoral degree
- Research
- University
1d
Associate Dentist Blacktown, New South Wales
Bupa —Blacktown NSW
7d
Associate Dentist
Campsie Family Dental —Campsie NSW
- $101,746.56 - $226,813.38 a year
- Part-time
- Clinic
- Bachelor's degree
- In-person
Quick Apply

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Start-up Associate (Clinical Trial Associate) - Sydney

Fortrea -
Sydney NSW

Apply Now

Job Details

Full-time
5 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

clinical associate jobs in parramatta nsw

Start-up Associate (Clinical Trial Associate) - Sydney

Client Advocate Executive - HIS

Senior Clinical Research Associate I (SCRA1) - Sydney, Melbourne, Adelaide or Brisbane

Regulatory and Study Start Up Clinical Trials

Senior Clinical Research Associate

Global Study Management (Senior) Associate (Global CTA)

Psychologist / Rehabilitation Counsellor

Data Engineer

Associate Sales Representative Sports Medicine - Newcastle

Postdoctoral Research Associate

Associate Territory Manager

Associate Dentist North Rocks, New South Wales

Territory Manager - Sydney South

Product Specialist | BD Pyxis

Territory Manager

Speech Pathologist – All Levels (Senior, Associate, Graduate)

Life Sciences Cyber Intelligence Analyst

Group Leader Immuno-Oncology

Associate Dentist Blacktown, New South Wales

Associate Dentist

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