Regulatory Affairs Jobs in Florida
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Search Results - Regulatory Affairs Jobs in Florida
Katalyst Healthcares & Life Sciences-Tampa
US equivalent).
A minimum of 3 years' experience in Regulatory Affairs
Advanced experience in the areas that may include preparation of dossiers for product registrations outside the US; preparation of submissions to the FDA strongly preferred...
resume-library.com -
RECRUITMENT PROFESSIONALS LTD-Miami
vertical.
Verticals are: QA / Regulatory Affairs / Clinical Dev & Ops / Commercial / CDMO / Engineering within the UK, EU and US markets.
Requirements to join are a proven track record in vertical market recruitment, preferably international life sciences...
mindmatch.ai -
Gvw Group, Llc-Miami
agreements, and non-compete clauses.
7. Regulatory Affairs:
Ensure compliance with industry-specific regulations and standards.
Liaise with regulatory bodies and manage regulatory filings and submissions.
Qualifications:
• Juris Doctor (JD) degree from...
appcast.io -
Ultimate Staffing-West Palm Beach
sales, and regulatory affairs, to ensure seamless coordination and communication throughout the shipping process.
• Work with confidential customer information.
• Build sustainable relationships and trust with customer accounts through open communication...
mindmatch.ai -
Lifelancer-Tampa
with R&D, regulatory affairs, quality, and commercial teams to ensure clinical program alignment with business objectives.
Participate in project team meetings and provide clinical updates and scientific insights.
Support product development...
resume-library.com -
Orlando
Demonstrates competency in regulatory affairs as defined by department-specific requisite skills.
• Prioritizes clinical trial needs based on trial status, participant, and departmental needs
• Practices effective problem identification and resolution...
orlandohealth.com -
Tallahassee
and accrediting organizations.
• Works with regulatory affairs to ensure documents required for compliance and regulatory submissions are complete.
• Assists in the development and implementation of new procedures and regulatory requirements
• Facilitates...
icims.com -
Miami
required medical information, including query generation, tracking, and follow up with reporters (research and post-market).
• Liaise with clinical operations, medical/drug information, regulatory affairs, clinical research organizations (CRO), study sites...
icims.com -
Miami
with clinical operations, medical/drug information, regulatory affairs, clinical research organizations (CRO), study sites, affiliates and data management groups regarding safety data collection and data reconciliation as required.
• Ensure compliance...
icims.com -
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