In-Demand Clinical trial manager Jobs in Concord Nsw

Senior / Clinical Research Associate
IQVIA —North Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trial Project Manager - Feasibility (Cell Therapy)
AstraZeneca —Macquarie Park NSW
- Full-time
- Bachelor's degree
- Recruiting
- AI
4d
SCRA / Site Engagement Manager - FSP
Fortrea —Sydney NSW
- Full-time
- Patient monitoring
- Bachelor's degree
- No degree
Clinical Data Associate
Avance Clinical —Sydney NSW
- Full-time
- Nursing
- Management
- Research
Quick Apply
Senior Clinical Research Manager
Medtronic —Sydney NSW
- Full-time
- Management
- Master's degree
Account Manager - Maternal Infant Care
GE HEALTHCARE —Mascot NSW
- Sales
- Salesforce
- Microsoft Office
12d
Research Coordinator for Trauma Service
Northern Sydney Local Health District —Sydney NSW
- $87,813 - $116,824 a year
- Full-time
- Nursing
- No degree
- Time management
4d
Senior Clinical Trials Coordinator
Ramsay Health Care —Kogarah NSW
- Part-time
- Management
- Referral program
Quick Apply
Clinical Operations Leader (CTM) - FSP
Parexel —North Ryde NSW
- Master's degree
- Education
- Bachelor's degree
- Work from home
Study Start-Up Manager
Novo Nordisk —Sydney NSW
- Bachelor's degree
- Negotiation
Clinical Project Manager (Oncology)
Tardis Group —Sydney NSW
- Management
- Research
- Presentation skills
Clinical Trials Coordinator
Western Sydney Local Health District —Sydney NSW
- $44.28 - $58.91 an hour
- Full-time
- Organisational skills
- Communication skills
3d
Regulatory Submissions Associate Manager II - APAC
Fortrea —Sydney NSW
- Full-time
- Hybrid work
- Bachelor's degree
3d
Clinical Research Associate (I) and (II)
Novo Nordisk —Sydney NSW
- Patient monitoring
- Clinic
- Bachelor's degree
Research Coordinator for Trauma Service
NSW Health —St Leonards NSW
- $1,682.93 - $2,238.93 a week
- Full-time
- Nursing
- No degree
- Time management
4d
Manager/Senior Manager, Regional Clinical Compliance
BeiGene —Sydney NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trials Coordinator
NSW Health —Blacktown NSW
- $44.28 - $58.91 an hour
- Temporary
- Organisational skills
- Communication skills
3d
Clinical Research Associate
IQVIA —Sydney NSW
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Study Start Up Manager
AstraZeneca —Macquarie Park NSW
- Full-time
- Hybrid work
- Bachelor's degree
- No degree
- Organisational skills
10d
Research Genetic Counsellor
The Garvan Institute of Medical Research —Sydney NSW
- $85,000 a year
- Part-time
- Blood sampling
- Research
- Databases
- Parental leave

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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 trial manager jobs in concord nsw

Senior / Clinical Research Associate

Clinical Trial Project Manager - Feasibility (Cell Therapy)

SCRA / Site Engagement Manager - FSP

Clinical Data Associate

Senior Clinical Research Manager

Account Manager - Maternal Infant Care

Research Coordinator for Trauma Service

Senior Clinical Trials Coordinator

Clinical Operations Leader (CTM) - FSP

Study Start-Up Manager

Clinical Project Manager (Oncology)

Clinical Trials Coordinator

Regulatory Submissions Associate Manager II - APAC

Clinical Research Associate (I) and (II)

Research Coordinator for Trauma Service

Manager/Senior Manager, Regional Clinical Compliance

Clinical Trials Coordinator

Clinical Research Associate

Study Start Up Manager

Research Genetic Counsellor

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