In-Demand clinical study start up Jobs in sydney nsw

Senior / Clinical Research Associate
IQVIA —North Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Study Start-Up Manager
Novo Nordisk —Sydney NSW
- Bachelor's degree
- Negotiation
Clinical Project Coordinator
Medtronic —Macquarie Park NSW
- Full-time
- Communication skills
Senior Study Start Up Associate
ICON Plc —Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
- Dental insurance
Clinical Site Associate / Clinical Trial Associate
ICON Plc —Sydney NSW
- Full-time
- Microsoft Office
- Administrative experience
- Bachelor's degree
- Health insurance
- Dental insurance
2d
In House CRA
ICON Plc —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
- Communication skills
- Health insurance
- Dental insurance
Experienced Study Start Up Specialist
ICON Plc —Sydney NSW
- Full-time
- Bachelor's degree
- No degree
- Budgeting
- Health insurance
- Annual leave
Clinical Research Coordinator
GenesisCare —St Leonards NSW
- Full-time
- Nursing
- Vital signs
- Microsoft Office
7d
CTA 1
IQVIA —North Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
9d
Radiation Oncology Medical Physicist Registrar | Temporary
Western Sydney Local Health District —Sydney NSW
- $42.11 - $59.98 an hour
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
12d
Research Assistant – Research Officer
The Garvan Institute of Medical Research —Sydney NSW
- Up to $117,400 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Medicine
- Parental leave
Clinical Operations Leader (CTM) - FSP
Parexel —North Ryde NSW
- Master's degree
- Education
- Bachelor's degree
- Work from home
Project Coordinator / Officer
The Garvan Institute of Medical Research —Sydney NSW
- Up to $95,000 a year
- Full-time
- Laboratory
- Doctoral degree
- Microsoft Office
- Parental leave
13d
Clinical Research Associate
IQVIA —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Advanced Trainee
NSW Health —Randwick NSW
- $117,745 - $147,664 a year
- Full-time
- Medicine
- Research
- ICU experience
- Annual leave
- Parental leave
12d
Research Officer
The Garvan Institute of Medical Research —Sydney NSW
- Up to $108,000 a year
- Full-time
- Doctoral degree
- Research
- Education
- Parental leave
Start Up Lead APAC
Precision for Medicine —Sydney NSW
- Remote
- Management
- English
- Bachelor's degree
Quick Apply
Laboratory Manager
The Garvan Institute of Medical Research —Sydney NSW
- Up to $125,000 a year
- Full-time
- Microsoft Excel
- Management
- Data analysis skills
- Parental leave
Senior / Site Activation Specialist
IQVIA —North Sydney NSW
- Full-time
- Bachelor's degree
- No degree
- Organisational skills
Aboriginal Traineeship - Wardsperson
Nepean Blue Mountains Local Health District —Sydney NSW
- $25,045.71 - $43,386.48 a year
- Full-time
- Education
- Communication skills
- Employee assistance program
9d

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Senior / Clinical Research Associate

IQVIA -
North Sydney NSW

Apply Now

Job Details

Full-time

Qualifications

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

Full Job Description

Sydney North, Australia | Full time | Hybrid | R1525252

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 study start up jobs in sydney nsw

Senior / Clinical Research Associate

Study Start-Up Manager

Clinical Project Coordinator

Senior Study Start Up Associate

Clinical Site Associate / Clinical Trial Associate

In House CRA

Experienced Study Start Up Specialist

Clinical Research Coordinator

CTA 1

Radiation Oncology Medical Physicist Registrar | Temporary

Research Assistant – Research Officer

Clinical Operations Leader (CTM) - FSP

Project Coordinator / Officer

Clinical Research Associate

Advanced Trainee

Research Officer

Start Up Lead APAC

Laboratory Manager

Senior / Site Activation Specialist

Aboriginal Traineeship - Wardsperson

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