Responsibilities include, but are not limited to:
- Assist with Process Improvements documentation
- Assist with audits (both internal and external as needed).
- Assist with the timely delivery of validation deliverables.
- Coordinate with department leaders on project deliverables.
- Assist with monitoring training delivered to Medrio personnel regarding GCP, 21 CFR Part 11, and other important topics.
Skills/Areas of Experience:
- Bachelor’s degree or relevant experience.
- Knowledge of the clinical trials industry.
- Knowledge of clinical trial technologies.
- Excellent communication and interpersonal skills.
- Ability to liaise successfully with project teams.
- Familiarity with Microsoft Word, Excel, PowerPoint.
- Familiarity with GCP, 21 CFR Part 11
- Experience in or with software company operations is ideal but not required.
About Medrio:
Medrio's SaaS offering is a key component in the pipeline of getting lifesaving drugs to the people who need them. We automate the clinic trial process and offer significant advantages over the competition: 75% lower cost, setup in days rather than months, and much better ease of use. Founded in 2005 we are privately owned, profitable, and are currently experiencing geometric growth in terms of customers, revenue, and employees. We believe in wellness! Medrio covers the cost of employee premiums for medical, dental, vision, life and LTD insurance, gym membership, and we promote an atmosphere of work/life balance, including flexible work schedules and unlimited PTO.
The Medrio team is made up of individuals with a wide array of skills and interests, but all have a passion for providing the best possible user experience for our customers. We are looking for smart, collaborative, creative, and conscientious people to help us expand our product capabilities and better serve our customers.
To see detailed information on the data we collect during the application process, and how Medrio complies with data privacy laws, visit our Careers page.
Salary Range: $60,000 - $70,000
Top Skills
What We Do
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Medrio delivers integrated eClinical software designed specifically for pharmaceutical, biotech, medical device, diagnostics, and animal health markets. Our innovative electronic data capture (EDC), eSource, eConsent, and ePRO products empower our customers to reduce costs and timelines so that CROs can increase their trial volume and sponsors can bring products to regulatory submission faster.
Since our founding in 2005 as the first cloud-based EDC system, we’ve become known throughout the market for our easy-to-use solutions and for delivering speed and simplicity to our customers’ clinical trials. Medrio users can build their databases in an average of 2.8 weeks with no programming required, make mid-study changes with just a few clicks of a mouse, and much more. Our innovative software, as well as the robust and flexible training, onboarding, and support resources we provide our customers, have earned us a 98% customer satisfaction rating.
Medrio is the market leader in early phase trials and serves over 600 customers globally, with headquarters in San Francisco and offices across the United States, Europe, and Asia.
Visit medrio.com for more information.
