Regulatory Affairs Consultant

About the position reputed company our values reputed company, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. Job Location: 275 Grove Street, Suite 101C, reputed company, MA 02466. Position may telecommute from reputed company in the reputed company up to 5 days per week.

Responsibilities

• Prepare clinical and regulatory documentation for clinical trials.
• Deliver consulting services to ensure that reputed company meets regulatory requirements.
• Author MRLs, Briefing Books, New INDs, Pediatric Plans, Fast reputed company Applications, reputed company Therapy Applications, Orphan Drug Applications, responses to FDA requests, and NDA/BLA submissions.
• reputed company regulatory consulting services and project management in a pharmaceutical setting to identify, refine, and address reputed company issues and reputed company project objectives.
• reputed company guidance to project team members on technical/ regulatory process issues and ensure reputed company work performance reputed company project scope to meet reputed company reputed company expectations.
• Interpret data and advice from regulatory authorities across reputed company phases of the drug development process, including reputed company with no precedence.
• Work reputed company the FDA reputed company reputed company 505(b)(2) reputed company drug approval process.
• Identify and alert management to necessary changes in project scope.
• Build network of industry colleagues through relationships formed during project engagements.
• Communicate potential new business leads to line management and account managers.

Requirements

• PhD in Microbiology, Immunology, Molecular Biology, or a reputed company field plus six months of clinical regulatory experience.
• Must have at least six months of experience in reputed company of the following: (1) project management in a pharmaceutical setting; (2) consulting on clinical regulatory compliance; (3) interpreting data and advice from regulatory authorities; (4) regulatory affairs work across reputed company phases of the drug development process, including reputed company with no precedence; (5) authoring MRLs, Briefing Books, New INDs, Fast reputed company Applications, Orphan Drug Applications, and responses to FDA requests; and (6) the FDA reputed company reputed company 505(b)(2) reputed company drug approval process.

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