In-Demand Clinical research associate Jobs in St Leonards, Nsw

Senior / Clinical Research Associate
IQVIA —North Sydney NSW
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Research Associate
ICON Plc —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
- Communication skills
- Health insurance
- Dental insurance
Clinical Trial Research Coordinator
University of Sydney —St Leonards NSW
- $103,185 - $111,237 a year
- Full-time
- Research
- Databases
- University
8d
Clinical Research Associate II - Sydney
Fortrea —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
Clinical Research Associate
IQVIA —Sydney NSW
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Clinical Trial Coordinator
St Vincent's Hospital Network —Sydney NSW
- $114,251 - $134,809 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Office
13h
Clinical AI Research Assistant
Insight Timer —Sydney NSW
- Overtime
- Remote
- Doctoral degree
- Research
- Master's degree
Quick Apply
Clinical Trial Coordinator
NSW Health —Darlinghurst NSW
- $114,251 - $134,809 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Office
1d
Clinical Research Coordinator
GenesisCare —St Leonards NSW
- Full-time
- Nursing
- Vital signs
- Microsoft Office
4d
Clinical Trial Coordinator
St Vincent's Health Australia —Inner West NSW
- $114,251 - $134,809 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Office
1d
Clinical Trials Assistant - Operations
Chris O’Brien Lifehouse —Camperdown NSW
- Full-time
- Research
- Microsoft Office
- Administrative experience
- Gym membership
3d
Clinical Data Associate
Avance Clinical —Sydney NSW
- Contract
- Nursing
- Management
- Research
Quick Apply
Research Assistant - Eating Disorders Clinical Research
University of Sydney —Camperdown NSW
- $89,755 - $100,495 a year
- Full-time
- Microsoft Excel
- Research
- Analysis skills
5d
Clinical Trial Assistant (1 Year Contract)
IQVIA —North Sydney NSW
- Contract
- Administrative experience
Study Coordinator - Clinical Trials
Chris O’Brien Lifehouse —Camperdown NSW
- $15,900 a year
- Full-time
- Employee assistance program
4d
Clinical Research Nurse
Canopy Clinical Research —Leichhardt NSW
- $80,000 - $90,000 a year
- Full-time
- Nursing
- Microsoft Office
- Administrative experience
Quick Apply
9d
Clinical Research Associates
AstraZeneca —Macquarie Park NSW
- Contract
- Patient monitoring
- Bachelor's degree
- No degree
8d
Medical Oncology Clinical Trials Coordinator
NSW Health —St Leonards NSW
- $1,682.93 - $2,238.93 a week
- Temporary
- Microsoft Excel
- Microsoft Access
- Management
5d
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
5d
Senior/Clinical Research Associate
Precision Medicine Group —Sydney NSW
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel

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Senior / Clinical Research Associate

IQVIA -
North Sydney NSW

Apply Now

Job Details

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Patient monitoring
Bachelor's degree
Computer skills
Financial management
Communication skills

Full Job Description

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree in scientific discipline or health care.
Requires at least 1 year of on-site monitoring experience.
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Candidates will be assessed according to their years of experience and be considered for various levels where applicable.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

Refine Your Search

clinical research associate jobs in st leonards, nsw

Senior / Clinical Research Associate

Clinical Research Associate

Clinical Trial Research Coordinator

Clinical Research Associate II - Sydney

Clinical Research Associate

Clinical Trial Coordinator

Clinical AI Research Assistant

Clinical Trial Coordinator

Clinical Research Coordinator

Clinical Trial Coordinator

Clinical Trials Assistant - Operations

Clinical Data Associate

Research Assistant - Eating Disorders Clinical Research

Clinical Trial Assistant (1 Year Contract)

Study Coordinator - Clinical Trials

Clinical Research Nurse

Clinical Research Associates

Medical Oncology Clinical Trials Coordinator

Medical Oncology Clinical Trials Coordinator

Senior/Clinical Research Associate

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