Join the Scientia Clinical Research (SCR) team

• State-of-the-art early phase clinical research facility located in The Bright Alliance Building, Randwick, NSW.
• Multi-functional team of Medical, Clinical, Nursing, Pharmacy, Laboratory, Quality and Data Management professionals. Highly experienced in the early development of new medical treatments.
• Supportive environment with encouragement to develop to your highest potential
• A Not For Profit Organisation offering salary packaging benefit entitlements

About Scientia Clinical Research 

Scientia Clinical Research (SCR) is the first publicly funded purpose built early phase clinical trials centre in NSW. Located in the Bright Alliance Building with the Nelune Comprehensive Cancer Care Centre and services of the Sydney Children’s Hospital. Co-located in a major research precinct with Prince of Wales Hospital, Royal Hospital for Women, UNSW Sydney and the Lowy Cancer Research Centre.

About the Role

As a clinical study coordinator, you will assist in conducting early phase (1/2) clinical research trials, centred on drug development for oncology patient populations. You will have excellent organisational skills and ensure that all the clinical trials are conducted according to trial specific protocols, GCP and SCR procedures. You will contribute to ensuring patient and participant safety, and the integrity of trial activities and data. You will work closely with a multi-functional SCR team of doctors, clinical project managers, pharmacists, clinical study co-ordinators, data managers, the study Sponsor teams and clinical research associates.

About you

To be successful for this position you will fulfil the following criteria.

• Previous experience in clinical trials, preferably as a Clinical Study Coordinator or Clinical Research Nurse.
• AHPRA registered nurse with minimum of 2 years postgraduate experience. 
• Experience oncology nursing would be preferred.
• Excellent written and communication skills to communicate and collaborate with a wide range of stakeholders in a multidisciplinary framework.
• Excellent planning and organizational skills, with ability to multi task.   
• Flexible and adaptable to changing work environment and business requirements and willingness to work as required to meet timelines (i.e. early hours, after hours, and weekends). 
• Commitment to quality, continuous improvement with excellent attention to detail.
• High ownership and accountability for trial portfolio execution;  self motivated and pro-active, with a bias for action and taking initiative in resolving problems and facilitating solutions. 
• Strong team player and willingness to help others in the team.
• Good working knowledge of clinical research, ICH GCP and the basics of drug development.
• Knowledge of ethics and governance processes, and competence in preparing and submitting trial documents is desirable. 
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If you would like more information about this opportunity, please contact careers@scientiaclinicalresearch.com.au and quote “Clinical Study Coordinator”.

Thank you for your interest.