The Opportunity
Join our dynamic team and make an impact in advancing Alzheimer's Disease research! As a Clinical Trial Coordinator, you'll play a pivotal role in delivering cutting-edge clinical trials from start to finish. You'll work independently while collaborating with a supportive team, ensuring clinical trials run smoothly and efficiently. Your expertise in Good Clinical Practice (GCP) will guide you as you manage patient recruitment, data collection, and documentation. With your attention to detail, you'll navigate complex procedures and maintain strong relationships with clinicians, patients, sponsors, and key stakeholders.
This is a Permanent Full-Time position based in Malvern, Victoria.
Benefits
* Market leading remuneration
* Salary packaging; $15,900 annually for living expenses, plus up to $2,650 each year for entertainment benefits.
* Flexible hybrid work arrangements in a friendly workplace with an emphasis on work life balance
* Additional training & career development opportunities
* Leave benefits – purchased additional annual leave
* Reward and Recognition Program
* Fitness Passports: Full facility access can include gyms, group classes and pools for yourself and your family.
* Free independent and confidential counselling sessions and free wellbeing resources and webinars available through our Employee Assistance Program in multiple languages.
* Exclusive discounts at MyCar; Servicing, Brakes, Repairs, and Tyre Care Plans
* Exclusive commercial discounts for JB HI-FI and The Good Guys
Responsibilities:
* Managing key trial activities including recruitment, screening and on-study safety and efficacy visits.
* Practicing essential clinical documentation and data management processes according to Good Clinical Practice.
* Performing study specific procedures (ie. venepuncture, cognitive rating scales, ECGs).
* Conducting general administrative duties associated with clinical trial maintenance (ie. ensuring ISF is maintained; responding to queries).
What do we need from you?
* At least 12 months prior experience in clinical trial research.
* Excellent understanding of GCP.
* Excellent record keeping skills with a keen eye for detail.
* Ability to work independently and as part of a team (including demonstrated organisational and problem-solving skills).
* Excellent communication skills, written and verbal.
* Strong administrative and computer skills.
Desirable:
* Dementia clinical trial experience.
* Cognitive rating scale experience (including CDR, ADAS-Cog, MMSE, NPI etc.)
* Venepuncture, cannulation and ECG experience.
* GCP certification.
Ready to make a change? Apply Now by completing the application and attaching your CV & Cover letter!
Ready to make a change? Apply Now!
All short-listed applicants will be asked to consent to a criminal record check.
For more info on DSA, check out our website:
HammondCare is committed to creating an inclusive workplace that promotes and values diversity and inclusion. We strive on creating an equal employment environment where everyone from any background can be themselves.
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