In-Demand Clinical research associate Jobs in Bondi Junction, Nsw

Clinical Research Associate II - Sydney
Fortrea —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
Clinical Research Orthoptist
University of Sydney —Sydney NSW
- From $93,345 a year
- Part-time
- University
- Working with children
- Bachelor's degree
2d
Research Assistant - Eating Disorders Clinical Research
University of Sydney —Camperdown NSW
- $89,755 - $100,495 a year
- Full-time
- Microsoft Excel
- Research
- Analysis skills
11d
Clinical Trials Study Coordinator
NSW Health —St Leonards NSW
- $46.05 - $61.27 an hour
- Temporary
- Communication skills
22h
Clinical AI Research Assistant
Insight Timer —Sydney NSW
- Overtime
- Remote
- Doctoral degree
- Research
- Master's degree
Quick Apply
Clinical Research Nurse
Canopy Clinical Research —Leichhardt NSW
- $80,000 - $90,000 a year
- Full-time
- Nursing
- Microsoft Office
- Administrative experience
Quick Apply
Clinical Trials Study Coordinator
Northern Sydney Local Health District —Sydney NSW
- $46.05 - $61.27 an hour
- Part-time
- Communication skills
1d
Medical Oncology Clinical Trials Coordinator
Northern Sydney Local Health District —Sydney NSW
- $87,813 - $116,824 a year
- Full-time
- Microsoft Excel
- Microsoft Access
- Management
11d
Clinical Research Associate II
PSI CRO —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick Apply
4d
Clinical Data Associate
Avance Clinical —Sydney NSW
- Contract
- Nursing
- Management
- Research
Quick Apply
Clinical Trials Assistant - Operations
Chris O’Brien Lifehouse —Camperdown NSW
- Full-time
- Research
- Microsoft Office
- Administrative experience
- Gym membership
9d
Study Coordinator - Clinical Trials
Chris O’Brien Lifehouse —Camperdown NSW
- $15,900 a year
- Full-time
- Employee assistance program
10d
Senior/Clinical Research Associate
Precision Medicine Group —Sydney NSW
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trial Coordinator
St Vincent's Hospital Network —Sydney NSW
- $114,251 - $134,809 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Office
6d
Research Assistant CP Global Clinical Trials Network
Cerebral Palsy Alliance —Camperdown NSW
- Full-time
- Research
- Administrative experience
- Organisational skills
Clinical Research Associates
AstraZeneca —Macquarie Park NSW
- Contract
- Patient monitoring
- Bachelor's degree
- No degree
13d
Associate Clinical Project Manager
IQVIA —North Sydney NSW
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trials Assistant
Chris O’Brien Lifehouse —Camperdown NSW
- Full-time
- Microsoft Office
- Bachelor's degree
- Communication skills
- Employee assistance program
10d
Clinical Trial Coordinator II
Thermo Fisher Scientific —Sydney NSW
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Parental leave
- Employee assistance program
11h
Medical Oncology Clinical Trials Coordinator
NSW Health —St Leonards NSW
- $1,682.93 - $2,238.93 a week
- Temporary
- Microsoft Excel
- Microsoft Access
- Management
11d

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Clinical Research Associate II - Sydney

Fortrea -
Sydney NSW

Apply Now

Job Details

Full-time

Qualifications

Patient monitoring
Bachelor's degree
Clinical trials

Full Job Description

We’re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.

As a CRA2, you will play a key role in managing and monitoring clinical trials, ensuring compliance with regulatory requirements, and fostering strong relationships with investigative sites. This is a fantastic opportunity for professionals looking to grow their career in a dynamic and collaborative environment.

Summary of Responsibilities:

Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.
Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
Prepares and implements project plans related to Clinical Monitoring responsibilities.
Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.
Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.
Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.
Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.
Ensures adherence to global quality control and CRA performance metrics.
Ensures audit readiness at site level.
Acts in the project role of a Lead CRA as assigned.

General On-Site Monitoring Responsibilities:

Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study. Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
Ensure the integrity of the source data reported by careful source document review. Monitor data for missing or implausible data.
Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.
Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.
Travel, including air travel, may be required and is an essential function of the job.
Prepare and submit accurate and timely trip reports.
Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.
Assist with the administration of clinical research projects, recruiting investigators (if applicable), collecting investigator documentation and site management.
Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems.
Track IP shipments and supplies, as needed.
Track and follow-up on serious adverse events as assigned.
Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.
Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.
Attend investigators’ meetings (if applicable), project team meetings and teleconferences, and others as needed.
Present training content for site initiation.
Assist with training of new employees (e.g., co-monitoring).
All other duties as needed or assigned.

Qualifications (Minimum Required):

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.
Thorough knowledge of monitoring procedures.
Basic understanding of the clinical trial process.
Fluent in local office language and in English, both written and verbal.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). AND
Typically 2 years of onsite clinical site monitoring experience (SIV - Close out).
Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines.
Ability to work with minimal supervision.
Have an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
Good planning, organization, and problem-solving abilities.
Works efficiently and effectively in a matrix environment.

Physical Demands/Work Environment:

Location: Incumbent of the role needs to be based in Sydney hand happy to work 3 days from the office if not travelling
Will involve outside of normal office hours as required by the role.
Travel Requirement is 60% of the time (traveling to study sites).

Learn more about our EEO & Accommodations request here .

Apply Now

Refine Your Search

clinical research associate jobs in bondi junction, nsw

Clinical Research Associate II - Sydney

Clinical Research Orthoptist

Research Assistant - Eating Disorders Clinical Research

Clinical Trials Study Coordinator

Clinical AI Research Assistant

Clinical Research Nurse

Clinical Trials Study Coordinator

Medical Oncology Clinical Trials Coordinator

Clinical Research Associate II

Clinical Data Associate

Clinical Trials Assistant - Operations

Study Coordinator - Clinical Trials

Senior/Clinical Research Associate

Clinical Trial Coordinator

Research Assistant CP Global Clinical Trials Network

Clinical Research Associates

Associate Clinical Project Manager

Clinical Trials Assistant

Clinical Trial Coordinator II

Medical Oncology Clinical Trials Coordinator

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