
Clinical Research Associate
1 week ago
As a clinical research coordinator, you will work closely with principal investigators, co-investigators, and the research team to conduct clinical research activities through coordination and delivery of direct and indirect care, as well as associated data collection for clinical trials.
Key Responsibilities- Coordinate timely start-up and smooth running of allocated trials onsite, documenting and monitoring progress with support from research leads, the start-up team, and your clinical lead.
- Collaborate with the team lead and local research team to ensure all recruitment targets and timelines are met.
- Build relationships with key stakeholders, including your team, research leads, principal investigators, centre staff, and sponsors.
- Work with patients, attending all trial assessments and treatments within your competency.
- Perform clinical tasks such as vital signs, ECGs, venepuncture, medication management as deemed competent, and maintain proficiency.
- Process samples, coordinate sample collection, and dispatch as required.
- Prepare for and host monitoring and close-out visits.
- Maintain up-to-date knowledge in regulatory, administrative, and clinical frameworks, as well as current clinical issues and practice related to research.
- Ensure all research is conducted in accordance with good clinical practice guidelines, study-specific protocols, and applicable national and international laws and regulations.
- Australian health practitioner registration with relevant nursing experience.
- Minimum 2 years' experience in clinical research coordinator-nursing, science or phase 1 research, oncology or nuclear medicine with an equivalent undergraduate degree.
- Strong computer literacy with knowledge of clinical trials software and ms office suite.
- Excellent communication and interpersonal skills, with ability to work independently and as part of a team in an effective, proactive, and cooperative manner.
- High level of initiative and flexibility, with ability to meet deadlines while balancing multiple priorities.
- Knowledge of good clinical practice and applicable national and international laws and regulations.
- Flexibility in working times and locations.
- Ongoing training and professional development opportunities.
- A supportive and collaborative team environment.
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