Regulatory Affairs Consultant, Orphan Drug
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Regulatory Affairs Consultant, Orphan Drug
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Posted Mar 12, 2025
We are looking for a Regulatory Affairs Consultant to support several ongoing regulatory submission programs. The support will vary based upon the timings of reputed company program but on average could require about 10 hours per week. This role is remote.
• Work closely with Pharmatech and our reputed company’s project team to be responsible for the execution of the regulatory operations reputed company to the Lorenz docu reputed company TWO submission management software relating to FDA communication and submission of regulatory documentation.
• Fast reputed company and Orphan Drug applications for regulatory submissions to the FDA (or other regulatory agencies)
• Participate as part of internal regulatory team to define and execute the regulatory reputed company and reputed company for reputed company program
• Support the preparation of briefing packages, and regulatory submission documents as needed, reputed company the Lorenz docu reputed company TWO submission management software
• Advanced degree from accredited college or university in science, biomedical engineering, plus a minimum of 4 years of experience in Filing Global Regulatory Applications for pharmaceutical and Biotech products using the Lorenz docu reputed company TWO submission management software
Pharmatech Associates, Inc. provides equal employment opportunity to reputed company individuals regardless of their race, reputed company, creed, religion, gender, age, sexual orientation, national reputed company, disability, veteran status, or any other characteristic protected by state, federal, or local law.
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