Nurse Study Coordinator
4 days ago
**Be part of leading research and development**:
- ** Work with a collaborative team, people helping people**:
- ** Some flexibility required***
Our client, PCRN Limited is a private research facility, with six sites across New Zealand. Running clinical trials across all therapudtic areas, each site is staffed by a small, dedicated team. PCRN believe in promoting a supportive work environment to ensure its staff members feel valued. Located in central Christchurch, they are within walking distance to the amenities the inner city provides. Bringing new treatment opportunities to a community of volunteers is what makes working with them so rewarding.
The role of Study Coordinator is a specialised and important role, administering the day-to-day requirements of clinical trials. The Study Coordinator works collaboratively under the direction of a Principal Investigator.
The Study Coordinator will:
- _ Ensure compliance with protocols are followed_
- _ Comply with standard of care, consent and documentation requirements_
- _ Assist in developing study guidelines_
- _ Work within set study timelines, completing tracking requirements_
- _ Work directly with patients and caregivers_
- _ Assess patient eligibility for trials_
- _ Communicate with laboratories and record adverse events_
- _ Administer medication as directed_
- _ Take laboratory samples, record and distribute samples_
- _ Complete all administration requirements associated with clinical trials to a high standard_
- _ Ensure participant reimbursements are documented and paid on time_
- _ Liaise with external vendors/companies_
This role offers a
**We are particularly looking for**:
- _ Experience with clinical trials (preferable, but not essential)_
- _ Nursing experience is _preferable, however the role would suit new graduates with an interest in clinical research_
- _ Vaccinator certificate an advantage_
- _ Experience completing venesection procedures_
- _ Flexible, ability to meet changing requirements associated with the nature of clinical trials (including early morning and weekend work at times)_
- _ Someone who is self-managing, who can manage times and tasks to meet strict protocols and KPI’s of the trial_
- _ Excellent administration and computing skills_
- _ High attention to detail, a meticulous records manager as there is a lot of administration involved in the role_
- _ A person who can show genuine compassion for patients_
**RECRUITMENT INFORMATION**
You must be currently located in New Zealand and have the legal right to work here. A good command of the English Language and strong written communication skills are essential.
- CONFIDENTIALITY ASSURED_
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