At a Glance
- Tasks: Monitor clinical studies and ensure data integrity while supporting life-changing research.
- Company: Join Premier Research, a community dedicated to improving patient lives through innovative research.
- Benefits: Flexible work environment, continuous learning, and the chance to make a real impact.
- Other info: Diverse team culture with opportunities for growth and collaboration.
- Why this job: Be part of a team that transforms breakthrough science into new medicines and devices.
- Qualifications: Undergraduate degree in a health-related field or equivalent experience required.
The predicted salary is between 70000 - 70000 $ per year.
Premier Research is looking for a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here.
What you'll be doing:
- Deliver quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines.
- Maintain submission of expenses according to travel and expense requirements within company guidelines.
- Monitor (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations.
- Plan day-to-day activities for monitoring of a clinical study and sets priorities per site.
- Prepare for and conduct on-site qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites as required by clinical monitoring plan.
- Maintain Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization's processes per filing guidelines. Understand the required essential documents according to ICH/GCP Section 8. Review site documents and verifies they are accurate, complete, current, and include required updates.
What we are searching for:
- Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.
- Previous experience as a CRA required.
- This position requires current working rights for Australia.
Why Choose Premier? Premier Research is more than a company – it's a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems. Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies. As a Premier team member, you have the power to make an impact, regardless of job title and location. Our dedication to biotech and specialty pharma is unlike any other. We provide our staff with innovative technologies and continuous learning.
Clinical Research Associate II in Sydney employer: Premier Research Group
At Premier Research, we pride ourselves on being an exceptional employer that values the contributions of our Clinical Research Associates. Our supportive work culture fosters professional growth and encourages innovation, allowing you to make a real impact in the biotech and medtech sectors. With flexible working arrangements and a commitment to work-life balance, we empower our team members to thrive both personally and professionally while playing a crucial role in advancing life-saving medical solutions.
