Job Description

Job Header

Clinical Trials Assistant - Part time

Advertiser: IQVIAMore jobs from this company

Job Information

Job Listing Date
23 Mar 2020
Location
Sydney, Ryde & Macquarie Park
Work Type
Part Time
Classification
Healthcare & Medical, Clinical/Medical Research

Clinical Trials Assistant - Part time

As a Clinical Trials Assistant for a dedicated large Global Pharmaceutical within our single sponsor team you will provide administrative support to clinical projects and update clinical systems and databases. You will also 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. This is a part time role of 16 hours a week and can be flexible as and when this is done.

Responsibilities include:

  • Set up and maintain applicable TMF (both electronic and hard copy versions). Alert management where current status of data quality or performance is at risk to noncompliance.Study Start-up
  • Maintain, update, and input information and/or documents into applicable databases for clinical trial and/or data tracking; ensure reporting system records and quality standards are appropriately maintained.
  • Track incoming and outgoing clinical and regulatory documents/updates for investigator sites, studies, or project team
  • Support assigned group(s) or team(s) in preparing applicable study documents.
  • Manage central inbox and process site requests to appropriate team members and serve as the primary point of contact for field monitoring staff and global DRA.
  • Order supplies to support all phases of clinical studies

Skills and experience required:

  • Relevant Degree or equivalent
  • Ideally 2 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) guidelines
  • Broad knowledge of applicable protocol requirements as provided in company training
  • Sound therapeutic and protocol knowledge

As a Clinical Trials Assistant you will be provided with continuous training and development to improve and grow your career in Clinical Research. Please apply via the link. Only successful candidates will be notified.

As a Clinical Trials Assistant for a dedicated large Global Pharmaceutical within our single sponsor team you will provide administrative support to clinical projects and update clinical systems and databases. You will also 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. This is a part time role of 16 hours a week and can be flexible as and when this is done.

Responsibilities include:

  • Set up and maintain applicable TMF (both electronic and hard copy versions). Alert management where current status of data quality or performance is at risk to noncompliance.Study Start-up
  • Maintain, update, and input information and/or documents into applicable databases for clinical trial and/or data tracking; ensure reporting system records and quality standards are appropriately maintained.
  • Track incoming and outgoing clinical and regulatory documents/updates for investigator sites, studies, or project team
  • Support assigned group(s) or team(s) in preparing applicable study documents.
  • Manage central inbox and process site requests to appropriate team members and serve as the primary point of contact for field monitoring staff and global DRA.
  • Order supplies to support all phases of clinical studies

Skills and experience required:

  • Relevant Degree or equivalent
  • Ideally 2 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) guidelines
  • Broad knowledge of applicable protocol requirements as provided in company training
  • Sound therapeutic and protocol knowledge

As a Clinical Trials Assistant you will be provided with continuous training and development to improve and grow your career in Clinical Research. Please apply via the link. Only successful candidates will be notified.

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