In-Demand Clinical associate Jobs in Parramatta Nsw

Start-up Associate (Clinical Trial Associate) - Sydney
Fortrea —Sydney NSW
- Full-time
- Office
- Bachelor's degree
4d
Senior Clinical Research Associate
PSI CRO —Sydney NSW
- Full-time
- Hybrid work
- Patient monitoring
- Microsoft Office
- Bachelor's degree
Quick Apply
3d
Senior Associate
DWF —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Office
- Analysis skills
- AI
- Parental leave
4d
Product Specialist | BD Pyxis
BD —North Ryde NSW
- Nursing
- Sales
- Salesforce
3d
Associate Dentist North Rocks, New South Wales
Bupa —North Rocks NSW
2d
Remote Occupational Therapist
Hallmark Occupational Therapy —Sydney NSW
- $77,000 - $120,000 a year
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- AI
Quick Apply
2d
Dentist | Natural Dentistry
Abano Healthcare —Gordon NSW
- Contract
- Education
- Communication skills
Quick Apply
Veterinarian
Vets Central —Sydney NSW
- Part-time
- Laboratory
- Bachelor's degree
- Patient care
- Parental leave
- Employee assistance program
Quick Apply
13d
Clinical Research Associate II
AbbVie —Sydney NSW
- Full-time
- Remote
- Patient monitoring
- Bachelor's degree
- Organisational skills
1h

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Senior Clinical Research Associate
PSI CRO —Sydney NSW
College/University degree in Life Sciences or an equivalent combination of education, training & experience. Proficiency in MS Office applications.
Quick Apply
3d

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Start-up Associate (Clinical Trial Associate) - Sydney

Fortrea -
Sydney NSW

Apply Now

Job Details

Full-time
4 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 .

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Refine Your Search

clinical associate jobs in parramatta nsw

Start-up Associate (Clinical Trial Associate) - Sydney

Senior Clinical Research Associate

Senior Associate

Product Specialist | BD Pyxis

Associate Dentist North Rocks, New South Wales

Remote Occupational Therapist

Dentist | Natural Dentistry

Veterinarian

Clinical Research Associate II

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