About the Company
Southern Cross Healthcare is New Zealand’s largest private hospital network, dedicated to providing exceptional healthcare services. With a strong commitment to patient well-being and clinical excellence, we operate facilities across the country, including a prominent hospital in Christchurch. Our mission is to enhance the health and well-being of New Zealanders through high-quality, accessible, and compassionate care. We foster a collaborative environment where innovation and professional growth are highly valued.
Job Description
We are seeking a dedicated and meticulous Clinical Research Coordinator to join our research team at Southern Cross Healthcare in Christchurch. In this vital role, you will be instrumental in the planning, execution, and completion of clinical trials, ensuring adherence to study protocols, regulatory guidelines, and Good Clinical Practice (GCP). You will work closely with investigators, patients, and sponsors, contributing directly to advancements in patient care and medical knowledge. This is an exciting opportunity to make a tangible impact within a leading private healthcare provider.
Key Responsibilities
- Coordinate and manage all aspects of clinical research studies, from initiation to close-out.
- Recruit, screen, and enroll eligible study participants according to protocol requirements.
- Obtain informed consent from participants and ensure ongoing understanding of the study.
- Collect, record, and maintain accurate and complete study data in electronic and paper formats.
- Schedule and coordinate participant visits, tests, and procedures as per the study protocol.
- Monitor participants for adverse events, document them, and report to the principal investigator and relevant authorities.
- Prepare and submit study documents to Institutional Review Boards (IRBs) or ethics committees.
- Liaise with study sponsors, monitors, and auditors during site visits and data queries.
- Manage study supplies, equipment, and investigational products.
- Ensure compliance with all applicable local, national, and international regulations and guidelines (e.g., GCP, ICH).
Required Skills
- Bachelor's degree in a health-related field (e.g., Nursing, Pharmacy, Life Sciences).
- Minimum of 2 years of experience as a Clinical Research Coordinator or similar role in a hospital or clinical setting.
- Demonstrated understanding of clinical trial processes, regulatory requirements, and ICH-GCP guidelines.
- Proficiency in medical terminology and clinical data management.
- Excellent organizational skills with meticulous attention to detail.
- Strong communication and interpersonal skills, with the ability to interact effectively with patients, colleagues, and external stakeholders.
- Ability to work independently and as part of a multidisciplinary team.
- Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
Preferred Qualifications
- Certification as a Clinical Research Coordinator (e.g., CCRP, CCRC).
- Experience with electronic data capture (EDC) systems.
- Familiarity with specific therapeutic areas relevant to hospital-based research (e.g., oncology, cardiology, surgery).
- Post-graduate qualification in a relevant field.
Perks & Benefits
- Competitive salary and superannuation scheme.
- Comprehensive health and wellness benefits, including private health insurance options.
- Generous professional development opportunities and funding for certifications.
- Access to modern research facilities and cutting-edge technology.
- Supportive and collaborative team environment.
- Employee assistance program.
- Opportunities for career advancement within a leading healthcare organization.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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