Clinical Trial and Pharmacovigilance Associate (CRO)
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| Company Name | Avion |
| Company Type | Private |
| Job Type | Part-Time |
| Salary Range | Market Competitive |
| Location | Perth, Western Australia, Australia |
| Qualifications | None / No Formal Education |
| Experience | 1 Year+ |
Job Overview
Avion is seeking a Clinical Trial and Pharmacovigilance Associate to join their team in Perth, Western Australia, Australia. This part-time role focuses on supporting clinical trials and pharmacovigilance activities within a full-service Contract Research Organisation (CRO), dedicated to integrated research, data management, and advanced imaging technologies.
Company Overview
Avion is a full-service Contract Research Organisation (CRO) and advanced Imaging specialist partner for clinical trials and medical research, headquartered in Perth, Western Australia, Australia. They are dedicated to integrated research, data management, and cutting-edge imaging technologies. Avion offers end-to-end solutions for clinical trials, from concept to completion, with extensive experience across broad therapy areas including Oncology, Dermatology, and Radiopharmaceuticals.
Quick Details
- Salary Range: Market Competitive
- Job Type: Part-time
- Qualifications: None / Open to all applicants
- Experience: 1 Year+
Key Responsibilities
- Support the execution and management of clinical trials according to protocols and regulations.
- Assist in pharmacovigilance activities, including adverse event reporting and safety data management.
- Contribute to data collection, quality control, and integrity for research studies.
- Ensure compliance with Good Clinical Practice (GCP) and other relevant guidelines.
- Collaborate with study teams to facilitate smooth trial operations and timelines.
- Participate in the preparation of study documentation and reports.
Requirements
- Experience or understanding of clinical trial processes and pharmacovigilance principles.
- Strong attention to detail and organizational skills.
- Excellent written and verbal communication abilities.
- Ability to work effectively in a team-oriented CRO environment.
- Proficiency in relevant software and data management tools.
- A commitment to ethical research practices and patient safety.
Benefits
- Opportunity to work in a leading Contract Research Organisation (CRO).
- Contribute to cutting-edge medical research and clinical trials.
- Gain valuable experience in pharmacovigilance and data management.
- Collaborative and supportive team environment.
- Professional development opportunities in the clinical research field.
- Flexible part-time work arrangements.