Senior Clinical Research Associate (Melbourne)
Senior Clinical Research Associate (Melbourne)
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Melbourne, Australia
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Posted: less than a week ago
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Description
Clinical Research Associate (CRA) – 0.2 FTE Location: New South Wales (NSW) or Melbourne, Australia. About the Role We are seeking a motivated and detail-oriented Clinical Research Associate (CRA) to join our team on a 0.2 FTE (one day per week equivalent) basis. This is an excellent opportunity for an experienced CRA looking for versatile, part‑time work while contributing to high-quality clinical research projects. Key Responsibilities
- Conduct site monitoring visits (remote and on‑site as required) in accordance with study protocols, ICH‑GCP, and regulatory requirements.
- Ensure data integrity and compliance through source data verification (SDV).
- Build and maintain strong relationships with investigational sites.
- Support site initiation, monitoring, and close‑out activities.
- Identify and elevate risks or issues impacting study delivery.
- Assist with regulatory document review and maintenance of Trial Master Files (TMF).
- Collaborate with cross‑functional teams to ensure smooth study execution. About You
- Previous experience as a Clinical Research Associate (or similar role).
- Strong understanding of ICH‑GCP guidelines and clinical trial processes.
- Excellent communication and organisational skills.
- Ability to work independently with minimal supervision.
- Located in NSW or Melbourne, with willingness to travel occasionally if required.
- Relevant degree in life sciences, nursing, or a related field preferred. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. #J-18808-Ljbffr Apply on Kit Job: kitjobau.com/job/3rvcs3
- Conduct site monitoring visits (remote and on‑site as required) in accordance with study protocols, ICH‑GCP, and regulatory requirements.
- Ensure data integrity and compliance through source data verification (SDV).
- Build and maintain strong relationships with investigational sites.
- Support site initiation, monitoring, and close‑out activities.
- Identify and elevate risks or issues impacting study delivery.
- Assist with regulatory document review and maintenance of Trial Master Files (TMF).
- Collaborate with cross‑functional teams to ensure smooth study execution. About You
- Previous experience as a Clinical Research Associate (or similar role).
- Strong understanding of ICH‑GCP guidelines and clinical trial processes.
- Excellent communication and organisational skills.
- Ability to work independently with minimal supervision.
- Located in NSW or Melbourne, with willingness to travel occasionally if required.
- Relevant degree in life sciences, nursing, or a related field preferred. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. #J-18808-Ljbffr Apply on Kit Job: kitjobau.com/job/3rvcs3
Highlights
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Company namePPG AUS ProPharma Group MIS
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Job positionSenior Clinical Research Associate (Melbourne)
More details
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This is a part-time job.
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