As a
Clinical Research Associate
(CRA) you are an essential part of the clinical operations team responsible for coordinating and overseeing the execution of studies and clinical trial according to the study protocol, ICH-GCP, applicable regulations, guidelines and sponsor requirements.
Some of what you will do:
Identify investigator sites and participate in the feasibility process for new studies
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e. ICH GCP
Perform visits remotely according to foreseen applicable procedures and timeframes
Interact with the Trial Start-up team and support collecting the documents or information necessary for the ethical and administrative submission
Work closely with the sites to ensure that the planned recruitment targets are in line with the study plan/projections and motivate Investigators to achieve the targets
Check the correct submission and completion of informed consent forms
Manage the progress of assigned studies by tracking regulatory submissions and approvals, case report form (CRF) completion and submission, and data query generation and resolution
Verify that responsible adverse events have been reported using a SAE form, according to OPIS and/or Sponsor procedures
Maintain all files and documentation pertaining to the studies and ensure that site documents are available for filing into TMF and correct archiving of files on study completion
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Requirements:
Enthusiastic,



knowledgeable and proactive
University degree in a scientific/life science field
At least 2 years of experience in managing and conducting clinical trials
In depth knowledge of ICH GCP principles
Able to carry out independently all the activities related to the monitoring of clinical trials
Good knowledge of Office Suite (Word, Excel, PowerPoint)
Organizational and problem-solving skills
Excellent written and verbal communication skills including good command of English language
Who we are:
Founded in **** in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects.
OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients' challenging achievements.
What we offer:
We offer a competitive salary with other benefits/bonuses and opportunity to develop your professional career with an expanding and growing company.
Please read the information notice on the processing of personal data in the candidates information section of
our company website.
This page is hosted by JazzHR and uses cookies for technical and analytical purposes. For details regarding the processing of your application data by OPIS, please refer to our:
Pivacy Policy
Candidate Privacy Policy

📌 Clinical Research Associate (Australia)
🏢 OPIS
📍 Australia