In this career summary, you will find out what the job of A Regulatory Affairs Associate is about and what it is like.
After reading this, you will have a good idea on what the job is about and decide if this is the right career for you.
Regulatory Affairs Specialists coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals, or registrations. May compile and prepare materials for submission to regulatory agencies.
Coordinate, prepare, or review regulatory submissions for domestic or international projects.
Provide technical review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, and clarity of presentation.
Review product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies.
Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents.
Regulatory Affairs Associates with little to no experience tend to make between $37390 and $48810 while the more experienced ones make over $84600 per year.
Top 5 paying states
1 of the easiest ways to increase your salary as A Regulatory Affairs Associate is to move to a higher paying state like DC. Right now, the highest paying states for Regulatory Affairs Associates are DC, MA, CT, NY and CA.
However a higher pay at DC doesn’t guarantee that you will make more because the living expenses at DC might be 2x higher than where you are currently at now.
3 other factors that can increase your salary as A Regulatory Affairs Associate is the degree you hold, the industry you work in and lastly the company you work for (bigger companies like the Fortune 500 companies tend to pay more).
They research market conditions in local, regional, or national areas, or gather information to determine potential sales of a product or service, or create a marketing campaign. May gather information on competitors, prices, sales, and methods of marketing and distribution.
They plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyze clinical data.
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