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Clinical Research Associate(FSP)

4 weeks ago


Melbourne, Victoria, Australia PanaCRO Full time

This range is provided by PanaCRO. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

A$100,000.00/yr - A$140,000.00/yr

Major Responsibilities and Duties
  • Overseeing the management and administration of all aspects of clinical trials/studies involved in each step of the clinical study.
  • Preparing protocols and other necessary documents required for trial approval by EC and obtaining EC approval on time.
  • Monitoring and coordinating the clinical trial conduction throughout the process by following GCP and SOP strictly.
  • Providing input for query resolution, site closure, and collection of documentation required for clinical trial reports after trial completion.
  • Ensuring EDC/CTMS systems are updated in a timely and accurate manner according to requirements.
  • Reporting and following up on all SAEs/adverse drug reactions in a timely manner according to internal SOPs.
  • Updating investigator files and trial master files.
  • Building and maintaining positive relationships with sites and investigators.
  • Ensuring site visit reports and correspondence are completed on time.
Qualifications
  • Bachelor's degree in biomedical/science discipline or equivalent (e.g., BSc, Registered Nurse, BPharm).
  • At least 3-10 years of clinical operation monitor experience for senior positions.
  • Good communication and organizational skills.
  • Proactive working attitude.
Company Overview

Panacro Pharmaceutical Technology Co., Ltd. is a contract research organization (CRO) specializing in pharmaceutical R&D and clinical studies. We provide solutions for clinical studies, IND, and NDA of chemical and biological drugs and vaccines.

Established in 2004, Panacro has served hundreds of clients across 20+ major therapeutic fields, with offices in 20 major provinces or cities in China.

We operate with comprehensive SOPs and a professional team adhering to international standards (ICH-GCP), maintaining close cooperation with 80% of study sites in China.

Our focus is on delivering high-quality, efficient services to shorten product marketing cycles and facilitate market entry.

Additional Details
  • Seniority level: Mid-Senior level
  • Employment type: Full-time
  • Job function: Healthcare Provider and Research
  • Industries: Wholesale Drugs and Sundries, Pharmaceutical Manufacturing

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