Clinical Trial Coordinator

Benefits

Opportunity for a registered nurse to transition into a clinical research role

Work with a small, close knit team

Flexible working arrangements

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About the company

This company is a medical research and development facility researching and formulating nutraceuticals and pharmaceuticals focused improving patients' lives with chronic diseases

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About the opportunity

The Clinical Trial Coordinator is responsible for the recruitment and coordination of clinical trials.

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Duties

Coordination in all areas of clinical research

Coordinating the initiation and implementation of clinical trials, including patient recruitment, assessments, follow ups, dispensing study medications, and taking body measurements

Collect and monitor clinical trial data to ensure quality control and fulfillment of good clinical practice criteria.

Submission to Ethics Committee and maintenance of ethics Documentation

Liaise with physicians, study team, scientists and patients to coordinate research visits and study procedures.

Observing and reporting any incidence of side effects associated with clinical trials

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Skills and Experience

Tertiary education in medical/biological/ science/ nursing or equivalent field.

Cert III in Pathology collection or proven experience in performing phlebotomy

Experience in the independent coordination of clinical trials and knowledge of ICH/GCP

Demonstrated organisational and planning skills.

Ability to work independently and part of a multidisciplinary team.

Excellent problem-solving skills and attention to detail.

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Culture

Small close knit team that are fun and focused

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How to Apply

Click apply or contact Christine Bristol, Executive Consultant on +61 2 8877 8766 for a confidential discussion.

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