Clinical Research Associate 2 (Melbourne)

Join a dynamic team driving cutting-edge clinical trials! As a CRA, you'll be the key link between sponsors and trial sites—ensuring studies run smoothly, data is accurate, and compliance is top-notch. As part of our Sponsor dedicated team you will join not 1 but 2 Globally Companies. This role is Perth or Brisbane based. Minimum of 18 months monitoring experience is required.

**Key Responsibilities**:

- Lead site visits (selection, initiation, monitoring, close-out) per GCP/ICH standards.

- Deliver protocol training and maintain solid site communication.

- Monitor site performance, escalate quality issues, and ensure regulatory compliance.

- Track study progress: submissions, enrollment, CRFs, and data queries.

- Maintain Trial Master File (TMF) and Investigator Site File (ISF).

- Document findings and follow-ups with clear, timely reports.

- Collaborate with cross-functional teams to support project execution.

- Manage site budgets and invoicing (if applicable).

**What You Bring**:

- Bachelor’s in science or healthcare (or equivalent experience).

- 2+ year of on-site monitoring experience. Haematology and Oncology

- Strong grasp of GCP/ICH and clinical trial protocols.

- Tech-savvy: MS Office, iPhone/iPad, and remote tools.

- Excellent communication, organization, and problem-solving skills.

- Ability to build solid relationships with sites and teams. Apply on Kit Job: kitjobau.com/job/3qmjvr