Sydney Clinical Research Coordinator

7 days ago

Sydney, New South Wales, Australia beBeeClinicalResearch Full time $85,708 - $115,569

Sydney Clinical Research Coordinator

We are seeking a highly organized and detail-orientated individual to join our team as a Clinical Research Coordinator in Sydney. As a Clinical Research Coordinator, you will play a crucial role in the management of clinical trials from initiation to close-out.

Key responsibilities include:

  • Organizing meetings and coordinating with investigators, sponsors, and other stakeholders;
  • Tracking and updating study metrics, including enrollment, retention, and follow-up rates;
  • Maintaining accurate and complete records, including study documents, participant data, and regulatory submissions;
  • Assisting with site payment and expense management, ensuring timely and accurate processing of payments;
  • Coordinating logistics for trial-related activities, such as drug supply, equipment, and materials distribution;
  • Providing administrative support for investigator meetings, including preparing meeting materials, taking minutes, and sending follow-up communications;

To be successful in this role, you will need:

  • A strong understanding of Good Clinical Practice (GCP), regulatory requirements, and clinical research protocols;
  • Excellent organizational, communication, and interpersonal skills;
  • Proficiency in Microsoft Office, including Excel, Word, and PowerPoint;
  • A basic knowledge of clinical trial management systems (CTMS) and electronic data capture (EDC) systems;

In return, we offer:

  • A competitive salary and benefits package;
  • The opportunity to work on high-profile clinical trials with leading pharmaceutical companies;
  • Professional development and training opportunities to enhance your skills and knowledge;
  • A dynamic and supportive work environment with a team of experienced professionals;

This is an excellent opportunity for someone who is passionate about clinical research and is looking to take their career to the next level. If you are a motivated and detail-orientated individual who enjoys working in a fast-paced environment, please submit your application today.

Required Skills:

  • Clinical research experience, preferably in a coordinator or assistant role;
  • Strong understanding of GCP, regulatory requirements, and clinical research protocols;
  • Excellent organizational, communication, and interpersonal skills;
  • Proficiency in Microsoft Office, including Excel, Word, and PowerPoint;
  • Basic knowledge of CTMS and EDC systems;

Benefits:

  • Competitive salary and benefits package;
  • Opportunity to work on high-profile clinical trials with leading pharmaceutical companies;
  • Professional development and training opportunities;
  • Dynamic and supportive work environment;

About Us:

We are a leading provider of clinical research services, dedicated to delivering high-quality results and exceeding client expectations. Our team of experienced professionals is committed to excellence, innovation, and customer satisfaction.

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