Clinical Research Coordinator
7 days ago
We are seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team at Icon Group. As a key member of our research team, you will be responsible for coordinating and conducting clinical trials, ensuring compliance with Good Clinical Practice and Icon policies.
Key Responsibilities- Provide high-level support to Icon Principal Investigators in the conduct and day-to-day management of clinical trials.
- Manage and conduct the clinical trial portfolio, including trial coordination, recruitment, participant and team member education, and communication.
- Ensure that clinical research carried out within Icon is conducted in accordance with Good Clinical Practice, the NHMRC National Statement, and Icon policies.
- Contribute to the financial management of the business unit to ensure that trial participants are tracked and patient payment data is submitted in a timely fashion.
- Communicate effectively with trial participants to ensure that trial-related procedures are booked appropriately and compliance to attendance for trial visits is maintained.
- Actively attend meetings with internal and external stakeholders.
We are looking for a driven and detail-oriented individual who can independently solve problems. With relevant research experience, you will have the ability to manage your workflow and build rapport with various stakeholders through strong effective communication.
What We Offer- Access to novated lease options via our partner RemServ.
- Lucrative company-wide Rewards Portal.
- Employee Assistance Program.
- Development Pathways.
- Online Courses.
- Access to paid parental leave and the ability to purchase annual leave.
At Icon Group, we are committed to creating an inclusive workplace for all employees. We encourage applications from all diverse backgrounds. Our work is always important and not always easy, and we know the secret ingredient is our incredible, supportive people.
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