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Our client is a network of hospital based clinical trial sites with over 20 years’ experience in clinical trials in Aotearoa – New Zealand. They test the efficacy and safety of the most innovative medicines, devices, and approaches to advance the standard of healthcare across New Zealand.
The role
Your role will be critical in providing support to the Operations Team to ensure the smooth running of all studies. Responsible for accurate data entry, data query resolution, liaising with the monitor, resolving monitoring queries and maintaining trial supplies, you will pride yourself in your ability to work autonomously whilst delivering results within required timeframes, under the guidance of a lead study coordinator.
Additionally, you will also be responsible for organising patient appointments, undertaking participant visits (where appropriate), assisting with recruitment, participant visit kit preparation, labelling, ordering and destruction. A multi-faceted role with an incredible team, all values driven to deliver organisation outcomes.
About you
Benefits
Please note you need to be living in NZ and have the right to work in NZ to be considered for this role.
Interested? Apply now.
Upload your CV to our database.
Please let us know where you are, or where you would like to be in the world so we can point you in the right direction.