Clinical Trials Co-Ordinator
vor 3 Wochen
Clinical Trials Co-ordinator (Dietician/Diabetes Educator) At Hunter Diabetes Centre / Aim Research , we are committed to providing our patients with individualised care needed to meet their health goals, by providing patients access to leading specialists in Endocrinology, Diabetes Education and Clinical Research.
We are a small close-knit team who take pride in our work and shared values.
We enjoy the fast-paced goal-driven environment and thrive on achieving the best possible outcomes for our patients.
In addition to our regular endocrinology clinic, we also conduct clinical trials across a broad range of therapeutic areas including, but not limited to, diabetes and its complications, cardiology, weight loss, and vaccines.
We are involved in local as well as global research projects, giving our patients access to cutting-edge medications and technologies.
About the Role
Due to growth in our clinical trials portfolio, we are recruiting for an experienced Clinical Trial Coordinator role to join our trials team.
The role would ideally suit a registered nurse or dietician, with a solid background in diabetes and weight loss.
The successful candidate must be highly motivated and feel confident to work autonomously within a multi-disciplinary team.
Your responsibilities will include scheduling participant visits; conducting study assessments and collecting data during scheduled visits; data entry and overall logistics management of the study.
A key aspect of the role requires building a rapport with participants along with ongoing communication with the Research team, so excellent communication and computer skills are essential.
The role may also include the provision of diabetes education to our Type 1, Type 2, and Gestational diabetes patients.
HDC is known for its use of diabetes technology, so a sound understanding of pumps and CGM is desirable.
We hope the successful candidate is as passionate about diabetes as the rest of the team.
Key attributes are excellent time management and planning as well as the ability to attract new trials and recruit patients.
There will be an integral role in patient contact throughout the course of the trials.
The role will be full or part time with an immediate start.
Key responsibilities will include:
Conducting clinical research protocols in accordance with ICH GCP guidelines Coordinating recruitment of participants to clinical trials Diabetes and dietetic patient education Coordinating and delivering the care of clinical trial patients as per specific protocol requirements Coordination of trial-related activities and performance of study assessments (including ECGs, cannulation, vaccinations, and blood draws) Coordination of study administration, including reporting, data management, and ethics submissions Demonstrated high-level interpersonal skills necessary for negotiating and liaising effectively with a diverse range of staff, patients, and other stakeholders Location: We are based in Newcastle, NSW.
Only apply if you live in the Newcastle/Hunter area.
Minimum Requirements:
You will require a degree in a health science (preferably Nursing or Nutrition and Dietetics) Previous experience in clinical trials is essential Outstanding written and verbal communication skills Outstanding attention to detail Venipuncture and cannulation skills/certification Good Clinical Practice certification Proven experience to work both independently and in a multi-disciplinary team Interested in joining our team?
If this opportunity sounds like the right fit for you and your experience, please forward your resume and a cover letter that tells us a little more about you.
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