Hematology Research Registrar

4 months ago

Christchurch, New Zealand Te Whatu Ora – Health New Zealand Waitaha Canterbury Full time

**_Kia hiwa ra Kia hiwa_**

**Mō mātou | About us**
- “Ko ngā tāngata, te mātua mahi_ - _Putting people at the heart of all we do”_

When you work with Te Whatu Ora Health New Zealand - Waitaha Canterbury District, you’re part of something very special. We plan, fund and deliver health services to the almost 600,000 people that live in the Canterbury region. We are committed to Te Tiriti o Waitangi and its principles by ensuring our partnership with Māori are at the forefront of all our conversations.

Facilities within Waitaha Canterbury District include:

- Christchurch Women’s Hospital
- Hillmorton Hospital and the Princes Margaret Hospital - Mental Health Services
- Burwood Hospital - Older Persons Health and Rehabilitation Services, including the Spinal injuries Unit
- Ashburton Hospital - General Hospital, south of Christchurch

You will gain world class experience with varied case mixes and a high level of medical education, training and supervision. With 600 Resident Doctors employed at Waitaha Canterbury, you will join a team committed to serving their community. You can learn more here

**Ko wai koe | About You**

Our Haematology service comprises of several sub-specialities with one being Clinical Trials. The service is seeking a Senior Registrar to join the Trials team for a period of 12 months. The successful applicant will work closely with our Clinical Trials team in performing Sponsor and Investigator initiated research and conducting clinical consultations. Currently we have over 12 active clinical trials.

There is also an opportunity to work in support of the other Registrars in support of the wider Haematology service.

**Ngā pūkenga me ngā wheako | Skills & Experience**
- You will have experience in a number of hospital departments including Haematology.
- An understanding and interest in clinical trials / research in order to act as a sub-investigator and or Principal Investigator covering;
- Keep track of drugs and distribute only as specified in the protocol
- Keeping careful records and maintain them for as long as the protocol dictates
- Ensuring progress, safety, financial, and a final report to the study sponsor.
- Serious adverse events reported immediately
- Update financial disclosures if any circumstances change during the study
- Ensuring all records are complete and easily accessible by FDA
- Knowledge and commitment of Te Tiriti o Waitangi and how the principles can be applied to health.
- A willingness to grow and further develop an equity lens and skillset, both to assist Māori and minority groups.

**Ngā hua | Benefits**
- Enhance your career with first class training and supervision from the Medical Education & Training Unit (METU)
- Be supported by our Resident Doctors’ Support Team (RDST)
- Access support at all hours, including after-hours support from the Clinical Team Coordinators and SMOs

You will need to submit:

- Electronic copies of your CV and covering letter, and
- Contact details for three referees (which will be contacted right away)

**Pandemic Vaccination Statement**
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