In-Demand Senior clinical research associate Jobs in Melbourne, Vic

Senior / Clinical Research Associate
IQVIA —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Clinical Research Associate - FSP Melbourne / Sydney
Fortrea —Melbourne VIC
- Full-time
- Management
- Patient monitoring
- Administrative experience
12d
Project Associate / Snr Project Associate
Avance Clinical —Melbourne VIC
- Full-time
- Nursing
- Analysis skills
- Bachelor's degree
Quick Apply
Associate Director of Clinical Services (ADCS)
Epworth —Richmond VIC
- Full-time
- Management
- Leadership
- Communication skills
Quick Apply
Donor Relations Manager
Cabrini Health —Malvern VIC
- Part-time
- Microsoft Office
- Organisational skills
- Communication skills
- Commuter assistance
11d
Senior Manager / Assoc Director, Quality Assurance
Gilead Sciences —Melbourne VIC
- Weekend availability
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Discipline Lead, Nursing
RMIT University —Melbourne VIC
- $176,883 - $227,847 a year
- Full-time
- Management
- University
- Experience working with children
10d
Discipline Lead, Medical Radiations
RMIT University —Melbourne VIC
- $176,883 - $227,847 a year
- Full-time
- Doctoral degree
- Research
- Supervising experience
Associate Feasibility Director
IQVIA —Melbourne VIC
- Full-time
- Remote
- Work from home
5d
Senior Lecturer (Practice), General Practice Academic Lead
Monash University —Box Hill VIC
- $150,841 - $173,931 a year
- Part-time
- Hybrid work
- Doctoral degree
- Research
- Leadership
Clinical Nurse Educator
Eastern Health —Box Hill VIC
- Part-time
- Microsoft Excel
- Research
- Microsoft Office
- Health insurance
- Employee assistance program
4h

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Senior / Clinical Research Associate

IQVIA -
Melbourne VIC

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

Melbourne, 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.

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

senior clinical research associate jobs in melbourne, vic

Senior / Clinical Research Associate

Senior Clinical Research Associate - FSP Melbourne / Sydney

Project Associate / Snr Project Associate

Associate Director of Clinical Services (ADCS)

Donor Relations Manager

Senior Manager / Assoc Director, Quality Assurance

Discipline Lead, Nursing

Discipline Lead, Medical Radiations

Associate Feasibility Director

Senior Lecturer (Practice), General Practice Academic Lead

Clinical Nurse Educator

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