Research Nurse

Job description

Established in 2020 through the merger of Auckland Clinical Studies (ACS) and Christchurch Clinical Studies Trust (CCST), NZCR is at the forefront of early-phase clinical research in New Zealand. With over 35 years of combined research excellence, we have successfully completed 750 trials involving 15,000 participants, showcasing our commitment to advancing medical research. Our physician-led, world-class research units in Auckland, Christchurch, Wellington, and Hamilton conduct complex studies in both healthy participants and patient populations. Partnering with global pharmaceutical and biotech companies, we deliver excellence in clinical research and explore potential new medicines. Recognizing the pivotal role of study participants, NZCR prioritizes their safety and comfort through detailed study information, expert clinical care, and comprehensive support services. The Role Part-Time 0.5 FTE, 20 Hours, Fixed Term 3 Months Key tasks of this appealing role include: Clinical Perform study related clinical activities i.e., venepuncture ECGs, monitor vital signs and perform other specialised nursing procedures as appropriate to the specific needs of the study and the individual subjects. To ensure biological samples are collected and processed as required for the study protocol and NZCR SOPs. Perform miscellaneous duties as assigned. These may include collation of study documents, faxing and photocopying of study documents, preparation of blood collection tubes. To ensure the safety and rights of the study participant is always protected. To ensure that all documentation is accurate and timely and is in accordance with the study protocol and ICH/GCP. Research To educate the clinical study participants in the requirements of the study according to the study protocol. To support study participants who choose to participate in clinical trials by providing advice and information and acting as the study participants’ advocate. To assess the study participant prior to trial treatment, monitor the study participant who has receive trial treatment and follow the study participant up on completion of trial treatment as required by the protocol. To report and record any adverse events (AEs) and serious adverse events (SAEs) that occur whilst the study participant is being treated on a clinical trial. Skills and Experience You must be a dedicated NZ Registered nurse. Exceptional communication skills – written and verbal. Venepuncture and IV certification experience is preferred but not essential as training will be given. Excellent clinical practice skills Good organisational skills – able to manage timeframes. Experience as a Research Nurse would be beneficial but not essential. Additional Information When you join us, we offer a range of benefits that work for you, your lifestyle and your career development which include: Boost Employee Benefits Programme: currently offering seventy-seven benefits, such as gym memberships, discounts for Torpedo7 and more. Engage in a vibrant workplace within a rapidly expanding company, providing opportunities for continuous learning, personal growth, and success. For more information about NZCR visit . If you are interested in this great opportunity and you are available, please click Apply for this job to submit your CV and cover letter. To apply for this role, you MUST be a NZ resident with a valid work visa. When you apply for this role, you are consenting to us sharing your information with our sister company, Optimal, where additional opportunities for career growth and development may arise.