Senior Director Regulatory Affairs Jobs in Florida
Senior Director Regulatory Affairs jobs in Florida are consistently active, driven by the state's large life sciences, pharmaceutical, and medical device sectors, with demand at every level from regulatory manager through vice president. Miami, Tampa, and Orlando anchor most of the hiring, where established employers like Johnson & Johnson, AbbVie, and Medtronic maintain significant Florida operations. The most in-demand specialties are FDA submissions, drug approval strategy, and Class II and III medical device compliance. Find a role that fits below and apply directly.
Find JobsOverview
Showing 5 of 15+ Senior Director Regulatory Affairs jobs
The Regulatory Affairs Assistant plays a crucial role in the clinical trial process by giving support and overseeing the daily regulatory activities by ensuring compliance with relevant regulations.
Principal Responsabilities:
- Prepare and maintain complete and accurate regulatory documents in support of clinical research studies.
- Manage all the communication with the IRB and Sponsor.
- Prepare each study-specific protocol, informed consent form, HIPAA authorization and other related documents for review by the IRB.
- Prepare and submit amendments, yearly requests for continuing approval of open protocols, audits, deviations, adverse event reports, and any other IRB-required submissions.
- Work with staff members to complete Financial Disclosure Forms for each study.
- Assist coordinators and site leadership in tracking the training status for existing staff, assisting with updates as needed.
- Maintain study binder, paper or electronic as appropriate, with all IRB related documents and correspondence for each study to always ensure audit readiness.
- Assist site leadership and coordinators in the preparation for monitoring visits, sponsor audits, and regulatory audits by conducting quality checks of the regulatory binder.
- Assist with the preparation and submission of closeout documents to the sponsors and IRBs including ensuring completeness, audit-readiness, and closure of the regulatory binder and appropriate archival of trial data.
- Submit or support SAE and AE submissions to the IRB as needed and in a timely fashion
Job requirements:
- Education: Bachelor's degree in Science or Administrative related fields.
- Languages: Bilingual (English and Spanish).
Pay: $20.00 per hour
Expected hours: 40.0 per week
Benefits:
- 401(k)
- Paid time off
Language:
- English (Required)
- Spanish (Required)
Work Location: In person
See All 15 Senior Director Regulatory Affairs Jobs in Florida
Find roles in Florida that match your experience and apply in just a few clicks.
Find JobsSenior Director Regulatory Affairs Jobs by City in Florida
Where Florida roles are concentrated, by current openings.
Senior Director Regulatory Affairs Job Market in Florida
A snapshot from current Florida openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Distribution & Wholesale
What Florida Employers Look For
The qualifications that appear most often in senior director regulatory affairs jobs across Florida.
- Bachelor's or advanced degree in life sciences, pharmacy, engineering, or a related field
- Minimum ten years of regulatory affairs experience, including at least three in a leadership role
- Deep working knowledge of FDA submission processes including INDs, NDAs, BLAs, and 510(k)s
- Proven ability to lead cross-functional teams and manage regulatory strategy across product lifecycles
- Experience with ICH guidelines, 21 CFR, and domestic and international regulatory frameworks
- RAC certification from the Regulatory Affairs Professionals Society strongly preferred by Florida employers
Senior Director Regulatory Affairs Jobs in Florida: Frequently Asked Questions
How do you become a senior director regulatory affairs in Florida?
Most senior director regulatory affairs roles in Florida require at least a bachelor's degree in a life science, engineering, or pharmacy field, with many employers preferring a master's or JD. Florida does not issue a state license specific to regulatory affairs, so advancement depends on accumulated FDA submission experience, cross-functional leadership, and the RAC credential from the Regulatory Affairs Professionals Society. Starting in a specialist or manager role at a Florida pharma, biotech, or medical device company is the typical path upward.
How much do senior director regulatory affairses make in Florida?
Senior director regulatory affairses in Florida earn a median of about $74,920 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $44,130 for the lowest 10% to over $127,420 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire senior director regulatory affairss in Florida?
Employers hiring senior director regulatory affairss in Florida right now include Arthrex, ITW, and Lupin, based on current listings on Migrate Mate as of September 2026. Florida's concentration of pharmaceutical manufacturers, medical device firms, and contract research organizations means demand for senior regulatory leadership is spread across the state rather than limited to a single hub.
Which Florida cities have the most senior director regulatory affairs jobs?
Coral Springs, Naples, and Florida have the most senior director regulatory affairs openings in Florida. Miami's dense pharma and biotech presence drives volume in the south, while Tampa and Orlando attract roles tied to large hospital systems, medical device companies, and regional headquarters that rely on dedicated regulatory leadership to manage FDA compliance and product approvals.
Are there remote senior director regulatory affairs jobs in Florida?
Yes, and more than most fields, since regulatory affairs work is documentation-heavy and strategy-focused rather than hands-on. About 29% of senior director regulatory affairs openings tied to Florida are remote or hybrid as of September 2026, reflecting how well the role translates to distributed teams. FDA submissions, labeling review, and regulatory strategy are the functions most commonly performed fully remote.
How can I get hired as a senior director regulatory affairs in Florida with little or no experience?
The most realistic entry point is a regulatory affairs specialist or coordinator role at a Florida pharmaceutical, medical device, or contract research organization, where you build direct FDA submission experience. Large Florida employers in the Tampa and Miami corridors regularly hire regulatory associates from life sciences graduate programs. Earning the RAC credential early signals commitment and gives candidates without years of experience a measurable edge when competing for roles at Florida-based manufacturers and CROs.
Where can I find and apply to senior director regulatory affairs jobs in Florida?
You can find and apply to senior director regulatory affairs jobs in Florida on Migrate Mate, which lists current Florida openings across the state's pharmaceutical, medical device, and biotech sectors. Find roles that fit your background and apply directly to the employers posting them.
See All 15 Senior Director Regulatory Affairs Jobs in Florida
Find roles in Florida that match your experience and apply in just a few clicks.
Find Jobs