Senior Clinical Research Associate
Senior Clinical Research Associate
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Job Description
Currently seeking Senior Clinical Research Associate for our Sponsordedicated team. Step into a dynamic role where youll drive innovation and excellence in clinical research. As a key player in our team youll ensure that study sites are not just compliant but thriving contributing to groundbreaking advancements in healthcare.
When you joinIQVIA AUSTRALIAas a sponsordedicated CRA youll enjoy the stability and resources of a leading global contract research organization while gaining direct experience with one of our customers.
With access to worldclass training and mentoring youll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
You must have a minimum of 4 years Independent onsite monitoring experience to be considered for this role. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.
You will be asked to complete a short video screening as part of the interview process.
Sydney and Melbourne are preferred locations but other Australian cities can be considered.
Essential Functions:
- Engage in Site Visits:From selection to closeout your visits will be pivotal in ensuring the success of our studies.
- Recruitment Strategies:Develop and implement innovative plans to recruit study subjects making a tangible impact on project outcomes
- Empower Sites with Knowledge:Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
- Champion Quality and Integrity:Evaluate and enhance site practices ensuring adherence to protocols and regulations.
- Drive Study Progress:Monitor every aspect of the study from regulatory submissions to data query resolutions ensuring seamless .
- Master Documentation:Keep meticulous records and ensure all site documents are perfectly maintained.
- Collaborate and Innovate:Work closely with a passionate team to support project and drive success.
- Manage Finances with Precision:Oversee site financials and ensure timely invoice retrieval.
Qualifications:
- Educational Excellence:Bachelors degree in a scientific or healthcare discipline preferred.
- Experience Matters:At least 4 years of onsite monitoring experience with preference for Oncology trial management exposure but not essential.
- Regulatory Savvy:Strong knowledge of GCP and ICH guidelines.
- TechSavvy:Proficiency in Microsoft Office and relevant technology.
- Communication Pro:Excellent written and verbal skills.
- Organized and Analytical:Strong organizational and problemsolving abilities.
- Time and Financial Management:Effective in managing time and finances.
- Team Player:Ability to build and maintain strong relationships with coworkers managers and clients.
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
Required Experience:
Senior IC
Employment Type
Full-Time
