A growing pharmaceutical regulatory affairs associate is to provide support for regulatory processes and procedures. Responsible for compliance and following cGMP protocols. Strategic Planning will include SOP development, review, investigate and conduct research on submissions. Will be working in premarket and postmarket protocols.
Preferred candidates will have the following:
BS in Chemistry, biology, health sciences, or other related sciences
3 years of Demonstrated experience in Health related fields
2 years of clinical setting work experience
Experience with regulatory is preferred
Attention to detail and a strong work ethic with a positive attitude.