Job Market Guide: Regulatory Affairs Specialist jobs in Raleigh-Durham (Fayetteville)

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in Raleigh-Durham (Fayetteville). Regulatory Affairs Specialists in Raleigh-Durham (Fayetteville) have between ${} and ${} years of experience, averaging $${} years of experience.

3 Regulatory Affairs Specialist jobs in Raleigh-Durham (Fayetteville)

Winston Salem, NC
The Quality Specialist IV has responsibility for GMP activities related to materials, production, product release, labeling, change control and post market monitoring activities for assigned RAI operating company. This individual will serve as the main quality contact between Contract Manufacturing Organizations (CMOs) and S&RA Quality Assurance group.
industry
Consumer Goods / Miscellaneous
experience
5 - 7 years

RESEARCH TRIANGLE PARK, NC
In this role, you will collaborates with sponsor, study start up, clinical and regulatory staff to ensure that all regulatory documents required for site IP approval are collected and reviewed in a timely fashion.
industry
Biotech/Pharma
experience
5 - 7 years

Durham, NC
In this role, the selected candidate will assist in the planning and design of internal studies (including feasibility studies), premarket clinical studies and post-market studies in support of US FDA and international regulatory submissions, as required.
industry
Business Services
experience
5 - 7 years