Remote Pharmacovigilance Specialist

Introduction to the Role

Do you have an eye for detail and a strong commitment to public health? As a Remote Pharmacovigilance Specialist, your expertise will help monitor and ensure the safety of pharmaceutical products in real-world use. This remote role offers the opportunity to combine your clinical expertise with regulatory precision, contributing to essential drug safety practices from anywhere in the world. With an annual salary of $96,145, this position offers both purpose and flexibility.

Key Responsibilities

• Monitor Adverse Events: Assess and process adverse drug reaction reports following global standards.
• Enter and Verify Data: Ensure all safety information is accurately recorded into pharmacovigilance systems.
• Identify Emerging Trends: Support signal detection and escalate concerns to safety management teams.
• Conduct Risk Assessments: Participate in the evaluation of product risks and the development of safety strategies.
• Generate Reports: Draft individual case safety reports (ICSRs) and prepare aggregate reports as required.
• Collaborate Across Functions: Engage with regulatory teams, medical experts, and external partners to ensure clarity and completeness of safety data.
• Maintain Documentation: Create well-organized safety narratives and contribute to continuous safety documentation.

Work Environment

In this fully remote role, you'll work in a structured yet flexible setting that values focus, accountability, and teamwork:

• Virtual Collaboration: Work closely with cross-functional teams spread across various geographies.
• Training Support: Access regular learning sessions on compliance, data entry accuracy, and case evaluations.
• Autonomy in Execution: Manage your workflows while adhering to pharmacovigilance timelines and protocols.

Tools & Technology

To fulfill your responsibilities effectively, you'll use specialized platforms that support pharmacovigilance compliance:

• Pharmacovigilance Systems: Familiar platforms may include Argus Safety, Oracle AERS, and ARISg.
• Compliance Portals: Contribute to regulatory submissions through global platforms like FAERS and EudraVigilance.
• Literature Monitoring Tools: Use PubMed and other databases for identifying safety data in scientific publications.
• Communication Platforms: Maintain collaboration through tools like Microsoft Teams, SharePoint, and secure email systems.

Required Qualifications

We're looking for a detail-oriented professional who brings structure and clinical insight:

• Bachelor's or Master's degree in Pharmacy, Nursing, Life Sciences, or equivalent
• At least 2 years of experience in pharmacovigilance within pharmaceutical or clinical research settings
• Familiarity with ICH E2B, GVP Modules, and FDA regulatory frameworks
• Proficiency in MedDRA, WHO-DD, and basic pharmacological terms
• Demonstrated ability to manage large volumes of safety cases
• Clear and concise written communication with strong documentation skills

Preferred Attributes

• Prior experience in post-marketing surveillance
• Remote work readiness and digital collaboration skills
• Certification in pharmacovigilance or clinical research
• Willingness to adapt to global time zone coordination

The Value You Bring

You will help strengthen the integrity of safety data by:

• Uncovering potential safety signals for pharmaceutical products
• Improving clinical outcomes through accurate safety evaluations
• Informing stakeholders on safety trends with well-supported findings
• Assisting in the evolution of labeling, dosage, and usage recommendations

Career Development

The Pharmacovigilance Specialist role offers long-term career possibilities:

• Learn cutting-edge tools and global regulatory standards
• Participate in case reviews across diverse therapeutic categories
• Grow into senior roles such as Safety Scientist, Benefit-Risk Analyst, or Regulatory Safety Expert

How We Define Success

• Consistent delivery of accurate and timely safety reports
• Proactive problem-solving and trend analysis
• Strong participation in cross-functional meetings
• Professional communication with internal and external partners

What Makes Remote Work Rewarding

• No commute means more time for focus and personal balance
• A flexible environment that values well-being and productivity
• Ability to make a meaningful contribution to global patient safety
• Empowerment through digital platforms and structured collaboration

Call to Action

Step into a role where your analytical mindset and clinical knowledge improve patient outcomes worldwide. If you're ready to support public health through informed vigilance, this position is your next opportunity.

Submit your application now and make your expertise count in global drug safety.