Remote Pharmacovigilance Specialist – Florida

Explore a Future in Drug Safety From Anywhere

Are you passionate about safeguarding patient health through data-driven vigilance? Imagine combining your pharmacovigilance expertise with a lifestyle that gives you the freedom to work from anywhere in Florida. This is your chance to join a cutting-edge team at the forefront of pharmaceutical safety, where innovation meets purpose. As a Remote Pharmacovigilance Specialist, you'll be more than just a safety gatekeeper; you'll become a key force in transforming real-world medical insights into actionable outcomes that influence global healthcare decisions.

Role Overview and Career Impact

Make a Global Difference

In this dynamic remote position, your focus will be the comprehensive evaluation of safety data, adverse event reporting, and regulatory compliance across diverse therapeutic areas. With modern pharmacovigilance platforms at your fingertips and support from an agile, multi-disciplinary team, your contributions will directly impact public health.

Real-World Responsibilities

From reviewing Individual Case Safety Reports (ICSRs) to assisting with signal detection and benefit-risk assessments, you’ll engage with the full scope of drug safety operations—all while embracing the flexibility of remote work.

Key Responsibilities and Functions

Vigilance and Reporting Activities

• Monitor, analyze, and document adverse drug reactions (ADRs) using validated pharmacovigilance software.
• Conduct timely data entry, quality review, and coding of ICSRs in compliance with global regulatory standards.
• Prepare detailed narratives and case summaries that contribute to global safety reports.

Safety Documentation and Regulatory Submissions

• Participate in the preparation of periodic safety update reports (PSURs), development safety update reports (DSURs), and risk management plans (RMPs).
• Support the creation of aggregate safety reports in collaboration with cross-functional teams.

Compliance and Risk Evaluation

• Maintain up-to-date knowledge of FDA, EMA, and ICH guidelines related to drug safety.
• Assist in signal management activities by gathering and analyzing safety trends from global data.
• Ensure all pharmacovigilance practices align with the company’s standard operating procedures and global regulatory expectations.

Work Environment and Daily Collaboration

A Connected Remote Experience

This is not your average home office gig. You’ll be immersed in a virtual ecosystem built on innovation and accountability. Expect a dynamic digital workplace that fosters transparency, peer feedback, and cross-departmental collaboration through platforms such as Microsoft Teams, Veeva Vault, and Argus Safety.

Seamless Communication Tools

Whether you’re collaborating during virtual case review meetings or brainstorming new risk mitigation strategies, you'll stay connected and engaged, without the commute.

Technologies and Platforms Used

Advanced Pharmacovigilance Tools

We’re not just paper-pushers with a safety database—we’re pioneers embracing technology to enhance every touchpoint of pharmacovigilance.

Safety Databases

• Argus
• ArisGlobal LifeSphere

Communication Tools

• Slack
• Microsoft Teams
• Zoom

Data & Analytics

• Spotfire
• SAS JMP
• MedDRA browser

Document Management

• Veeva Vault
• SharePoint

Regulatory Reporting Platforms

• EudraVigilance
• FDA’s FAERS
• MHRA Yellow Card

Required Qualifications and Competencies

Education and Work Background

• A bachelor’s degree in Pharmacy, Life Sciences, Nursing, or a related field (advanced degree preferred).
• At least 3 years of direct pharmacovigilance experience in pharmaceutical, CRO, or biotech environments.
• Previous remote experience is a plus, but not required—our onboarding team is here to support you.

Technical Expertise

• Solid understanding of medical terminology, ICH guidelines, and Good Pharmacovigilance Practices (GVP).
• Competency in coding systems like MedDRA and WHO Drug Dictionary.
• Familiarity with global pharmacovigilance regulations (FDA, EMA, PMDA).

Core Soft Skills

• Meticulous attention to detail combined with a strategic mindset.
• Strong communication skills for interfacing with global teams.
• A proactive, inquisitive nature with the confidence to ask, "What’s next?”

Opportunities for Professional Growth

Long-Term Career Trajectories

We don’t just offer jobs—we offer career journeys. As a Remote Pharmacovigilance Specialist, you’ll be exposed to real-time data challenges, novel drug development pipelines, and global compliance initiatives.

Internal Advancement

Opportunities for internal mobility are abundant, with pathways to roles like Signal Management Lead, Safety Science Manager, or even Pharmacovigilance Director. You’ll be encouraged to pursue certifications, join global safety symposiums, and contribute to publications that advance the field.

Cultural Values and Ethical Mission

A Human-Centered Company

We believe innovation and compassion are not mutually exclusive. We operate with integrity, celebrate diversity, and embrace creative thinking. Our people-first philosophy empowers remote professionals to deliver their best work while feeling connected to a global mission.

Our Collective Goal

We see every drug safety report as a story that could change someone’s life. And we know that people like you make those stories possible.

Compensation Package and Benefits

Competitive Salary and Perks

• Annual Salary: $142,465 (DOE)
• Comprehensive healthcare coverage (medical, dental, vision)
• Generous PTO, parental leave, and wellness days
• Retirement savings plan with company match
• Annual development stipend for continued learning
• Remote work tools provided (laptop, dual monitor setup, software licenses)

Call to Action: Make Your Mark in Global Drug Safety

This role is your ticket to a fulfilling career where science, compassion, and flexibility meet. You’ll join a team that’s setting new standards in drug safety—without being tied to a cubicle. If you’re ready to help shape the future of patient protection through pharmacovigilance, we want to hear from you.

Apply now and let’s create a safer world, one data point at a time.