
Clinical Trials Professional
3 days ago
**Clinical Trials Coordinator Role:**
We are seeking an experienced and motivated clinical trials professional to join our team.
This is an exciting opportunity for someone who prioritises teamwork, has a supportive and empathetic approach, and is able to listen to patients. The successful candidate will work closely with investigators to run clinical trials according to research protocols, ICH-GCP Guidelines, and applicable regulatory requirements.
Key Responsibilities:
- Attend Site Initiation Visits (remote and on-site) for delegated trials
- Prepare for and host site initiation, monitoring and close out visits
- Prepare and conduct participant visits
- Coordinate all aspects of allocated clinical trials
- Complete associated documentation, maintain study binders and other relevant documentation
- Maintain investigational product and perform accountability
- Maintain open and regular communication with sponsors, CRAs and monitors
- Complete all study close out activities including archiving of all study records
- Work with the recruitment team to ensure recruitment targets and timelines are met
The ideal candidate will have appropriate tertiary qualifications, experience working as a clinical trials coordinator, and a sound understanding of clinical trials and good understanding of clinical trial phases.
Requirements:
- Appropriate tertiary qualifications
- Experience working as a clinical trials coordinator
- Sound understanding of clinical trials and good understanding of clinical trial phases
- High level of attention to detail
- Ability to handle multiple tasks and prioritise effectively
- Familiarity with office-based computer packages
- Demonstrate excellent time management skills
- Team player
- Demonstrated high-level oral and written communication skills
Our organisation offers a supportive team environment, flexible working hours, immediate start, rewarding industry, staff discounts, conveniently located office, and employee assistance program benefits.
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