
Clinical Trials Specialist
24 hours ago
As a medical professional, you will have the opportunity to work on clinical trials and make a real impact in the world of medicine.
The ideal candidate will have completed at least two years of postgraduate medical training and be registered with AHPRA.
You will lead the informed consent process, conduct clinical assessments, and determine eligibility for study enrolment.
In this role, you will also monitor participants, provide medical care, and collaborate across departments to deliver safe clinical trials.
The successful applicant will have excellent communication skills and be able to work effectively in a team environment.
We offer flexible roles, including full-time and part-time positions, and require employees to be available to work 3-5 days per week across a 7-day rotating roster.
This role offers opportunities for professional growth, continuing professional development, employee recognition, and employee wellness initiatives.
Job Responsibilities:- Lead the informed consent process
- Conduct clinical assessments
- Determine eligibility for study enrolment
- Monitor participants
- Provide medical care
Required Skills and Qualifications:
- Completed at least two years of postgraduate medical training
- AHPRA registration
- Excellent communication skills
- Ability to work effectively in a team environment
Benefits:
- Flexible roles
- Full-time and part-time positions
- Professional growth opportunities
- Continuing professional development
- Employee recognition
- Employee wellness initiatives
About Us:
We are a dynamic organisation committed to advancing medicine and improving lives. We have successfully conducted over 1500 phase 1 clinical trials for biotechnology and pharmaceutical companies from around the world.
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