Clinical Trial Associate | CTA

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Position available for Clinical Trial Coordinator to move into a CTA role with top 5 CRO. Embedded with sponsor located in Macquarie Park area.

Summary about this job

Clinical/Medical Research

Company: PRA International- ANZ

Location: Sydney

Work type: Full Time

Salary: n\a

Phone: +61-8-9851-2176

Fax: +61-3-9896-7980

E-mail: n\a

Site:

Detail information about job Clinical Trial Associate | CTA. Terms and conditions vacancy

  • Office-based role
  • Experienced CTA candidates
  • Top 5 global CRO!

PRA Health Sciences is a globally recognized CRO working with leading Pharmaceutical sponsors across diversified therapeutic areas. We are focused on aiding the pharmaceutical industry in building a healthier future for all of us. Their success is dependent upon our ability to attract and retain a talented team of diverse professionals. Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages - yet operate in unison as one worldwide PRA community.

As a result of continued growth due to our success; a strong project pipeline and an influx of client work, we are currently seeking a talented Clinical Trial Associate to be based in Sydney.

Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation.

As a Clinical Trial Assistant, you will be dedicated to one of our global pharmaceutical client; with whom PRA shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in this exclusive program.

The Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials by supporting the Local Study Team in the coordination of logistical and administrative tasks at a local level. Our team help to speed the development of life-changing therapeutics and to make a distinctive contribution to the health and well-being of patients.

Key responsibilities in this role include:

  •  Supporting the Local Study Team collecting and tracking the documents and data required for regulatory submissions (contracts, financial agreements, patient informed consent forms, insurance certificates)

  • Maintaining and updating of the Trial Master File and preparation for relevant QC checks when applicable
  • Tracking site budget related matters, including processing invoices, tracking payments and also for scheduling meetings, updating Excel trackers, coordinating the translation of site documents

To be successful in this role, we are ideally seeking candidates with:

  • Tertiary qualifications in clinical or a life sciences related field (relevant experience/qualifications in similar professions may also be considered)
  • Highly organised, a problem solver and detail driven
  • Experience in the healthcare field, pharmaceutical industry or clinical research, preferably.
  • A degree level qualification in Life Science, have equivalent experience or be a licensed healthcare professional.
  • Fluent English, along with proficiency in the use of Microsoft Office suite

 

Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.

PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.

For more information please visit our website: www.prahs.com

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