In-Demand Clinical associate Jobs in Parramatta Nsw

Start-up Associate (Clinical Trial Associate) - Sydney
Fortrea —Sydney NSW
- Full-time
- Office
- Bachelor's degree
10h
Regulatory and Study Start Up Clinical Trials
Chris O’Brien Lifehouse —Camperdown NSW
- Full-time
- Organisational skills
- Communication skills
- Negotiation
- Employee assistance program
6h
Senior Associate
DWF —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Office
- Analysis skills
- AI
- Parental leave
19h
Product Specialist | BD Pyxis
BD —North Ryde NSW
- Nursing
- Sales
- Salesforce
7h
Associate Dentist
Demi Dental Green Square —Zetland NSW
- $13,700 - $18,000 a month
- Part-time
- Clinic
- Bachelor's degree
- EMR systems
Quick Apply
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
9d
Dentist
Grace Dental —Strathfield NSW
- Contract
- Patient care
- Communication skills
Quick Apply
Care Coordinator
Employment Hero —Sydney NSW
- Full-time
- AI
- Care plans
- Communication skills
- Work from home
- Parental leave
4h
Physiotherapist (Vietnamese Speaking Male)
Employment Hero —Bankstown NSW
- $100 - $110 an hour
- Temporary
- CPR Certification
- Management
- First Aid Certification
10h

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clinical associate jobs near parramatta nsw

Start-up Associate (Clinical Trial Associate) - Sydney

Fortrea -
Sydney NSW

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Job Details

Full-time
10 hours 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

Regulatory and Study Start Up Clinical Trials

Senior Associate

Product Specialist | BD Pyxis

Associate Dentist

Dentist | Natural Dentistry

Veterinarian

Dentist

Care Coordinator

Physiotherapist (Vietnamese Speaking Male)

I want to receive the latest job alert for clinical associate in parramatta nsw

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