Clinical Research Associate II/III - NZ

Overview The Clinical Research Associate (CRA II – CRA III) is primarily responsible for safeguarding trial participants' rights and wellbeing and ensuring reported trial data are accurate, complete, and verifiable from source documents. The CRA serves as the primary contact between Investigational Sites, Novotech, and Sponsor, functioning as a site relationship manager to ensure trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs. This role will be based in New Zealand , with hybrid working arrangements and flexible hours to support work–life balance. Minimum Qualifications & Experience Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Candidates should have strong time management, attention to detail, teamwork, and computer literacy. Experience in the research, pharmaceutical industry, or related field is required per job level as follows: CRA II: minimum of 6 months of CRA independent monitoring experience CRA III: 2+ years of CRA independent monitoring experience You must have full unrestricted working rights in NZ to be considered for this role . We unfortunately cannot provide sponsorship for this role. Responsibilities Build relationships with Principal Investigators, study coordinators, pharmacists, and site trial personnel to ensure efficient, expedited, and smooth management of clinical trials. Foster internal and external customer relationships to ensure focus on efficient, timely, and productive project delivery as per study requirements and timelines. Collaborate with IHCRA and Regulatory Start Up Associate (RSA), prepare site essential documents, and support ethics and regulatory submission and approval processes as needed. In collaboration with the Regulatory Start-up (RSU) Team, understand applicable local and international regulatory requirements relevant to specific trials. Support recruitment of participants as per site targets; drive site recruitment and engagement initiatives and update site-specific recruitment plans as required. Monitor investigational sites per ICH GCP, including Site Selection, Site Initiation, Site Monitoring, Site Close Out, unblinded pharmacy visits, and co-monitoring visits. Visits may be conducted onsite or remotely as per CMP. About Us Novotech is a global full-service clinical Contract Research Organization (CRO). Novotech is a globally recognized leader in clinical research and scientific advisory services, committed to fostering an award-winning workplace culture that values ambition, innovation, and growth. We have been named Employer of Choice, Great Place to Work, and Employer of Choice for Gender Equality (EOCGE). Since 1997, we have expanded to 30+ offices across Asia-Pacific, the United States, and Europe, uniting professionals from diverse backgrounds to advance therapies that improve patient outcomes worldwide. We offer mentorship opportunities, professional development programs, and flexible benefits to support work–life balance. We are committed to fostering an inclusive environment where everyone is treated with fairness and respect. We welcome applicants from diverse backgrounds and experiences. About the Team Novotech combines advanced therapeutic and regulatory expertise with a client-centric service model to provide a trusted, long-term partner for clients and an accelerated path to bring life-changing advances to market. Employees have the opportunity to develop their careers within a diverse, global organization and a collaborative culture. Strategic vs transactional mindset Ability to gain insights and make proactive decisions quickly Culture that fosters partnership and collaboration, where every voice is heard and valued Ongoing support from senior stakeholders and leadership Job Information Job Identification: 4034 Posting Date: 07/15/2026 Job Schedule: Full time Locations: Level 6, 2-6 Crowhurst Street, Newmarket, NZ #J-18808-Ljbffr