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Clinical Trials Assistant (R1075333) in St Leonards, Australia at IQVIA™

Date Posted: 5/7/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Experience:
    Not Specified
  • Date Posted:
    5/7/2019
  • Job ID:
    R1075333

Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

IQVIA is committed to bringing clients the best in creative problem solving, enabling healthcare companies to innovate with confidence, maximize opportunities, and ultimately drive human health forward.

We are searching for communicative candidates who are proactive and passionate about clinical research. 

A Clinical Trials Assistant will provide administrative support to clinical projects and update clinical systems and databases under direction of line manager and/or other designated clinical team members. Assists with general administrative functions as required.

To succeed in this position, candidates should have exceptional communication, computer, and problem-solving skills. You should be resourceful, analytical, adaptable, and organized with the ability to build rapport with peers and site staff.

Responsibilities include:

  • Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
  • Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. 
  • Assist with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
  • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.
  • May perform assigned administrative tasks to support team members with clinical trial execution
  • May Collaborate with Clinical Project Manager (CPM), CRAs/iCRAs and RSU on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. 

Skills and experience required:

  • High School Diploma or equivalent
  • Minimum of 3-4 years applicable experience or equivalent combination of education, training and experience  
  • Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Broad knowledge of applicable protocol requirements as provided in company training
  • Sound therapeutic and protocol knowledge

If you are interested in a Clinical Trials Assistant role with IQVIA please apply and one of our Talent Acquisition Recruiters will be in contact to discuss your application

Please submit an up to date resume with contact details, a cove letter is optional

Please note candidates MUST have full Australia working rights

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™



Job ID: R1075333