Learn More at: IQVIA.com
Connect with Us:

Clinical Trials Assistant - (1802008) in Sydney, at IQVIA™

Date Posted: 3/1/2018

Job Snapshot

Job Description

At Quintiles we help healthcare and biopharma companies improve their probability of success. We do this by connecting our scientific, therapeutic and analytics expertise with superior delivery. From advisory through operations, Quintiles and its affiliate companies is the world’s largest provider of product development and integrated healthcare services.
As one of FORTUNE’s ‘Most Admired Companies’ in 2016, we offer great opportunities for a career in world-leading clinical research. Our global projects, innovative tools and industry leading customers combined with outstanding support from our leadership team and clear career mapping allows you to make a difference in patient health.


IQVIA are currently looking for a dedicated Senior Clinical Trials Assistant OR Clinical Trials Assistant (depending on level of experience) to join our Site Management department. This is a full-time, on-going opportunity, and will be based out of the IQVIA Sydney office. The successful candidate will ideally have some prior experience within clinical trials in a similar role. We are only keen to hear from candidates looking to remain as a career CTA.
As a Clinical Trials Assistant (CTA) you will support the clinical project team in the following areas: accurately update and maintain clinical systems within project timelines;  prepare, handle, distribute, file, and archive clinical documentation and reports; review of study files periodically for accuracy and completeness; prepare, handle and distribute of Clinical Trial Supplies and maintenance of tracking information; track and manage Case Report Forms (CRFs), queries and clinical data flow.   May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.   Perform administrative tasks to support team members with clinical trial execution as needed. 

Job Requirements

To be considered you will ideally hold a Bachelors degree in a Scientific related field combined with:
- a general knowledge of applicable clinical research regulatory requirements; including GCP and ICH guidelines.
- Strong Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
- Strong written and verbal communication skills.
- Effective time management and organizational skills.
- Attention to detail and accuracy in work.
- Strong customer service orientation.
Prior experience working within clinical trials, as a CTA or within the pharmaceutical industry will be highly regarded.

In return you will have dedicated mentoring and training, and receive structured quarterly reviews on performance, promotion and bonus awards.  On top of this we offer initiatives around work life balance and fantastic reward and recognition programs, along with opportunities for growth and development.
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team
Connect to great opportunity™
IQVIA employees the opportunity to maximize their personal potential.

* Quintiles helped develop or commercialize 98 of the Top 100 best-selling products of 2014
* Quintiles has 36,000 employees conducting business in more than 100 countries
* Quintiles was named to FORTUNE’s World’s Most Admired Companies® 2016 list
* Quintiles was named as a 2016 World’s Most Ethical Company® by the Ethisphere Institute
Job ID: 1802008