Join our cutting-edge clinical research site network in New Zealand and step into the role of Quality Manager for Clinical Studies.
As the Quality Manager you will play a crucial role in ensuring that trials are conducted to the highest quality standards, with a focus on continual improvement and implementation of best practices.
With our presence across nine locations in New Zealand, you have the flexibility to choose to based anywhere in the country.
Sound like you?
Read more below.Please read the position details to the right and use the link below to apply for this job.PCRN is made up of a diverse team of experienced medical professionals dedicated to improving the health and well-being of our population.
PCRN conducts high-quality clinical trials for both NZ local and global pharmaceutical and biotech firms.
Taking advantage of the diverse landscape and population of New Zealand, PCRN provides unique opportunities for innovative treatment and world-class clinical trials.Working with us Clinical research helps improve lives.
At Pacific Clinical Research Network New Zealand, we are paving the way for the global availability of innovative medicines and treatments.The work we do showcases New Zealand as the country of choice for medical trials.
With 9 state-of-the-art partner facilities nationwide, we attract a diverse pool of participants, producing extensive high-quality data.
Responsive, caring and highly trained staff ensure consistently high safety and ethical standards across our network.
With centralised operations, our approach increases efficiency, reduces cost and risk, and produces better data for our clients.Our work is a vital step in making safe, effective treatments available to people around the world.
Backed by Pencarrow, one of New Zealand's most respected and experienced private equity companies, our goals for growth are exponential.Job Description Overview Location: New ZealandRole: Quality ManagerHours: Full-TimeDescription: Please see the position details below and the form at the bottom of the page to apply.For more information please email: ****** this role, you will ensure that trials are conducted to the highest quality, with continual improvement and implementation of best practices.
Compliance is a large focus of the role, as well as educating and mentoring the clinical team.
We have 9 site locations, meaning you can be based anywhere in New Zealand, although the preference would be for you to be based at one of the sites we would also consider someone working remotely with the right set up.Some of your responsibilities will include:Develop, implement and maintain a Quality Management System (QMS)Ensure trial participants and data are safeguardedTrain and mentor clinical staff to implement, review and maintain tracking of incidents within the trialsAdvise on corrective and preventative actions (CAPA's) to be implemented, ensuring these are carried out promptlyReview and ensure compliance with ethical and regulatory requirements and advise on improvement strategiesLead preparation for audit/inspections from external partiesDevelop and execute an internal risk-based QC/audit plan for systems and trials that includes the review of core trial documents to ensure compliance with policies, procedures and regulatory requirementsQualifications & Experience Previous experience within the healthcare sector in a similar roleGood knowledge of GCP and clinical researchNetworking and stakeholder management skillsProven ability to develop QC/audit plans and support auditsExceptional organisational skillsThe ability to travel around New Zealand and overseas if required on occasionWhat's in it for You?
Competitive Salary & Benefits Package Based on Your ExperienceExciting Time to Join a Business in a Huge Period of GrowthFull-Time Position with Flexible Hours For the Right CandidateOpportunity to Travel Around New Zealand + Potentially Overseas!Work within an Experienced, Diverse & Close-Knit TeamOngoing Opportunities for Professional Growth & DevelopmentImmediate Start Considered for the Right Candidate#J-18808-Ljbffr
