Posted in Other about 4 hours ago.
Location: REMOTE
Salary: $35.00 USD Hourly - $39.00 USD Hourly
Description:
Position Title: Associate Regulatory Affairs
Duration: Contract
Work Location: Remote
Description:
In this vital role you will assist the US Regulatory Leads and the Global Regulatory Team (GRT) in the Regulatory Affairs organization.
• To coordinate and execution of US regulatory submissions with the US Regulatory Lead in compliance with corporate standards and local regulatory requirements.
• To manage and execute of the preparation, delivery and electronic archiving of documentation for inclusion in US regulatory submissions
• To assist the Global Regulatory Lead to manage GRT interactions
The responsibilities of the Regulatory Affairs Senior Associate position are:
• Assist US Regulatory Lead to support regional regulatory activities (e.g. IND submissions and agency meetings)
• Provide and maintain CTA/MA documentation support (e.g. initial filings, amendments, and periodic reports) in collaboration with Regional Regulatory Lead
• Create and maintain product regulatory history documents through systems and appropriately archive all regulatory documents and agency communications
• Review regional component of the Global Regulatory Plan and provide input to operational deliverables
• Collaborate with CRO's / partners to support site initiation
• Coordinate collection of functional documents in support of regulatory filings
• Participate in GRT to support execution of regulatory strategy
• Coordinate QC of regulatory documentation (e.g. briefing materials)
• Provide primary authorship to routine regulatory correspondence (e.g. annual reports,
investigator packages)
• Prepare regulatory packages and cross-reference letters to support investigator initiated studies
• Complete regulatory forms to support agency communications
• Provide regulatory support through cross-functional interactions in work package teams (eg. commercial and evidence generation teams)
• Support process improvement initiatives, standards development, and metrics
• Assist in template development and maintenance
• Respond to specific requests from and communicate relevant issues to GRT
• Develop Regulatory Position with GRT
• Actively support regulatory compliance
• Support the development and execution of GRT goals
Top 3 Must Have Skill Sets:
• Strong communication skills - both oral and written
• Ability to understand and communicate scientific/clinical information
• Ability to deal with ambiguity
Motus |
Eurofins |
Ideal Industries, Inc. |