Overview

Clinical Regulatory Affairs AssociateAre 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 leaveWhat 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 FDASkills Needed for Consideration:* Associate degree (bachelors preferred)* Prior regulatory management experience* Experience working with a high-volume of records* Keen attention to detailLet’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 belowText: “regulatory” to Email: : ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee’s race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.Tracking

31.00

31.00

To Apply: https://www.jobg8.com/Traffic.aspx?kD%2boqxWZLdCCVUCf2%2fnAZQk