In-Demand Clinical trial Jobs in Caringbah, Nsw

Start-up Associate (Clinical Trial Associate) - Sydney
Fortrea —Sydney NSW
- Full-time
- Office
- Bachelor's degree
9d
Clinical Trial Coordinator
NSW Health —Darlinghurst NSW
- $81,748.17 - $121,497.00 a year
- Full-time
- Data analysis skills
- Research
- No degree
1d
Clinical Research Associate II
AbbVie —Sydney NSW
- Full-time
- Remote
- Patient monitoring
- Bachelor's degree
- Organisational skills
5d
Clinical Trial Coordinator (Registered Nurse) - Cardiology Department
NSW Health —Camperdown NSW
- $41.22 - $57.88 an hour
- Temporary
- Education
- Communication skills
- Nursing
- Parental leave
- Employee assistance program
1d
Clinical Trial Nurse
KG Talent —Sydney NSW
- Full-time
- Nursing
- Research
- Bachelor's degree
Quick Apply
Clinical Research Associate II
PSI CRO —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
Regulatory and Study Start Up Clinical Trials
Chris O’Brien Lifehouse —Camperdown NSW
- Full-time
- Organisational skills
- Communication skills
- Negotiation
- Employee assistance program
9d
Hospital Scientist Scientific Officer)
NSW Health —Darlinghurst NSW
- $79,433.52 - $113,298.98 a year
- Part-time
- Anatomy knowledge
- Microsoft Office
- Organisational skills
1d
Freelance Senior Clinical Research Associate
TFS HealthScience —Sydney NSW
- Contract
- Remote
- Nursing
- Patient monitoring
- English
Quick Apply
Senior Clinical Operations Manager
AbbVie —Sydney NSW
- Full-time
- Hybrid work
- Management
- Patient monitoring
- Bachelor's degree
5d
Senior Clinical Research Associate
PSI CRO —Sydney NSW
- Full-time
- Hybrid work
- Patient monitoring
- Microsoft Office
- Bachelor's degree
Quick Apply
9d
Counsellor - Community Outpatients – Drug Health Service, St Vincent’s Public Hospital, Sydney
NSW Health —Darlinghurst NSW
- $79,419 - $113,301 a year
- Part-time
- Microsoft Office
- Discharge planning
- Computer skills
1d
Biomedical Engineer
NSW Health —Darlinghurst NSW
- $128,143 - $140,954 a year
- Full-time
- Microsoft Office
- EMR systems
1d
Product Manager, Clinical Trials
Heidi —Sydney NSW
- Full-time
- Hybrid work
- EMR systems
- AI
- Work from home
- Parental leave
3d
Staff Specialist - Clinical Pharmacology & Toxicology
NSW Health —Darlinghurst NSW
- Part-time
- Doctoral degree
- Communication skills
- Teaching
- Employee assistance program
1d
Clinical Trials and Research Lead - Pharmacy
Ramsay Pharmacy —Sydney NSW
- Full-time
- Communication skills
Quick Apply
4d
Clinical Research Nurse
Western Sydney Local Health District —Sydney NSW
- $81,748.17 - $114,771.98 a year
- Full-time
- Communication skills
- Hospital experience
- Nursing
4d
Counsellor - Community Outpatients – Drug Health Service, St Vincent’s Public Hospital, Sydney
St Vincent's Hospital Network —Sydney NSW
- $79,419 - $113,301 a year
- Part-time
- Microsoft Office
- Discharge planning
- Computer skills
12d
Clinical Research Associate II - Sydney
Fortrea —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
Clinical Trials Assistant (Targeted)
University of Sydney —Camperdown NSW
- $89,755 - $100,495 a year
- Full-time
- Microsoft Office
- Administrative experience
- University
5d

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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

clinical trial jobs in caringbah, nsw

Start-up Associate (Clinical Trial Associate) - Sydney

Clinical Trial Coordinator

Clinical Research Associate II

Clinical Trial Coordinator (Registered Nurse) - Cardiology Department

Clinical Trial Nurse

Clinical Research Associate II

Regulatory and Study Start Up Clinical Trials

Hospital Scientist Scientific Officer)

Freelance Senior Clinical Research Associate

Senior Clinical Operations Manager

Senior Clinical Research Associate

Counsellor - Community Outpatients – Drug Health Service, St Vincent’s Public Hospital, Sydney

Biomedical Engineer

Product Manager, Clinical Trials

Staff Specialist - Clinical Pharmacology & Toxicology

Clinical Trials and Research Lead - Pharmacy

Clinical Research Nurse

Counsellor - Community Outpatients – Drug Health Service, St Vincent’s Public Hospital, Sydney

Clinical Research Associate II - Sydney

Clinical Trials Assistant (Targeted)

I want to receive the latest job alert for clinical trial in caringbah, nsw

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