Study Coordinator, Christchurch

Add expected salary to your profile for insights Be part of something new. Make a real impact in clinical research. Optimal Clinical Trials is expanding and we’re looking for an experienced Clinical Study Coordinator to join our brand-new, purpose-built research facility in the heart of Christchurch. This is your opportunity to work at the forefront of innovative healthcare, contributing to clinical trials that shape the future of medicine.Location: Christchurch Central, Canterbury Hours: 40 hours per week, Monday to Friday 8am - 4:30pm About the role: Reporting to the Research Manager, Site Lead, you’ll be responsible for managing the end-to-end delivery of clinical research trials. This is a hands-on role requiring confidence and experience in coordinating clinical studies. You’ll ensure that all research activities are conducted in strict adherence to study protocols, ICH GCP guidelines,and our Standard Operating Procedures (SOPs). As a Study Coordinator you will work closely with a multidisciplinary team of professionals and will play a key role in supporting and guiding junior team members, fostering a collaborative and high-performing environment.Key Responsibilities: Manage the setup, execution, and close-out of clinical research studies Ensure all activities comply with ICH GCP guidelines and Standard Operating Procedures Communicate with study sponsors, participants, and team members professionally and efficiently Contribute to the preparation of study reports, documentation, and presentationsTroubleshoot and resolve any operational issues that may arise during the study Key Requirements: Tertiary qualification in a relevant field (e.g. Life Sciences, Healthcare) Knowledge of Good Clinical Practice (ICH-GCP) guidelines Intermediate proficiency in Microsoft Office (Outlook, Word, Excel)Minimum of 12 months experience in clinical research An understanding of the significance and obligations under Te Tiriti o Waitangi We’re looking for someone who thrives in a dynamic environment, is highly organised, and has the ability to manage multiple moving parts. If you're passionate about clinical research and looking to contribute to the success of innovative studies, we’d love to meet you.Why Join Us? At Optimal Clinical Trials, we're not just another research organisation— we're a community of dedicated professionals driven by a shared vision of excellence. Here, you'll have the opportunity to make a real impact in a rapidly growing sector, surrounded by talented individuals who are passionate about their work and each other. Our core values of integrity, collaboration, and continuous improvement guide everything we do, creating a dynamic and supportive work environment where every day brings new challenges and opportunities for growth.If this sounds like you, please apply through our online application form with your CV and a cover letter. We look forward to receiving your application. Whilst we will endeavour to respond to each application, due to the volume of applicants this may not be possible. How do your skills match this job? How do your skills match this job? Sign in and update your profile to get insights.Your application will include the following questions: How many years' experience do you have as a Clinical Coordinator? Which of the following statements best describes your right to work in New Zealand? What's your expected annual base salary? How much notice are you required to give your current employer?How many years' experience do you have as a Study Coordinator? Are you willing to undergo a pre-employment medical check? Researching careers? Find all the information and tips you need on career advice. #J-18808-Ljbffr