Senior Clinical Research Associate

1 week ago


Vancouver, British Columbia, Canada 44.01 Premier Research S.R.L. Remote Work Freelance Full time
Senior Clinical Research Associate (Contractor)

Premier Research is looking for a Senior Clinical Research Associate (Contractor) to join our Global Clinical Monitoring and Site Management 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.

What You'll Be Doing:

- Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines.
- Maintains submission of expenses according to travel and expense requirements within company guidelines.
- Monitors (remote, onsite or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations.
- Plans day to day activities for monitoring of a clinical study and sets priorities per site.
- Prepares for and conducts on-site qualification, study initiation, interim monitoring and close-out monitoring visits at investigator sites as required by clinical monitoring plan.
- Maintains Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization's processes per filing guidelines. Has an understanding of the required essential documents according to ICH/GCP Section 8. Reviews 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 clinical research experience required and proven independent monitoring to include all visit types.
- At least 3+ years' experience in clinical trials monitoring.
- Compliant with the requirements of the Ministerial Decree.

This is a contract position with an anticipated contract duration of 6 months and with an immediate start.

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.

About Us

Premier Research is a global clinical research, product development, and consulting company. We are dedicated to helping biotech, specialty pharma, and MedTech innovators transform life-changing ideas and breakthrough science into new medical treatments. Our team is inspired by this common purpose. Premier is a place where you can change lives, and feel rewarded and celebrated. We aim high - we will not stop until we reach our goals. And we care about each other, about our customers and partners, and, most importantly, about all the patients that we touch with our work.

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