Job Description
Clinical Regulatory Affairs Associate
Are you well-versed in FDA regulations regarding medical testing equipment or similar biotechnology efforts? Do you have experience working in a highly-regulated industry and are familiar with reporting processes? If so, we would like to talk with you about this position as a Clinical Regulatory Affairs Associate. Apply now.
Perks of the Position:
* Long-term assignment
* $31 per hour, paid weekly
* Excellent skill building opportunity
* Ability to do incredibly meaningful work in today's society
* Access to health insurance and earned paid leave
What You Will Be Doing:
* Working with a high-volume of records & cases
* Reviewing critical documents & reports for completeness and accuracy
* Requesting edits and re-submissions as necessary
* Assuring the regulations and laws regarding IND submissions and financial disclosure meet compliance
* Preparing submissions to the FDA
Skills Needed for Consideration:
* Associate degree (bachelors preferred)
* Prior regulatory management experience
* Experience working with a high-volume of records
* Keen attention to detail
Let's make it as easy as possible for you to apply to be a Clinical Regulatory Affairs Associate in Scarborough. Simply choose the option below that is most convenient for you to get the conversation started.
Apply Online: see below
Text: "regulatory" to 207.560.0928
Email: [email protected]
Call: 207.774.8258