Regulatory Affairs Consultant

About the position reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same 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. Each 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 United States up to 5 days per week.

Responsibilities

• Prepare clinical and regulatory documentation for clinical trials.
• Deliver consulting services to ensure that the company meets regulatory requirements.
• Author MRLs, Briefing Books, New INDs, Pediatric Plans, Fast Track Applications, Breakthrough 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 client issues and reputed company project objectives.
• reputed company guidance to project team members on technical/ regulatory process issues and ensure timely work performance reputed company project scope to meet internal and external quality expectations.
• Interpret data and advice from regulatory authorities across reputed company phases of the drug development process, including projects with no precedence.
• Work reputed company the FDA Act reputed company 505(b)(2) pathway 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 each 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 projects with no precedence; (5) authoring MRLs, Briefing Books, New INDs, Fast Track Applications, Orphan Drug Applications, and responses to FDA requests; and (6) the FDA Act reputed company 505(b)(2) pathway drug approval process.

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