Clinical Trial Coordinator | Alzheimer’s Disease

at  HammondCare

ABOUT 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.

The Clinical Trial Coordinator manages the administration and conduct of Alzheimer’s Disease clinical trials. This is a Permanent Full Time position based in Malvern, Victoria.

Duties include:

• 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).