Pharmacovigilance Scientist

Pharmacovigilance Scientist

Company Type: EarlyStage US Startup

Location: Remote

Experience: 1 Year (6 months internship/project experience accepted)

Education: B Pharm (Mandatory)

Role Overview
The Pharmacovigilance Scientist will serve as a core contributor to scientific content creation, safety data evaluation, and support product development. This is not a traditional PV operations role this position blends scientific rigor with analytical thinking, business acumen, and creative problemsolving. You will build foundational scientific assets, analyze data, develop presentations, and support crossfunctional initiatives that shape the company's growth.

We are seeking a B Pharm graduate who is ambitious, proactive, and eager to grow with the organization. Exceptional performance will lead to expanded responsibilities and accelerated career progression.

Key Responsibilities

• Safety Data Evaluation Review, interpret, and summarize safety data, literature, and clinical information to support product development and regulatory strategy.
• Scientific Content Development Author highquality scientific documents, reports, summaries, and presentations for internal and external stakeholders.
• Data Visualization Create charts, graphs, dashboards, and visual summaries to communicate complex information clearly.
• CrossFunctional Collaboration Work closely with product engineering to align scientific insights with product strategy.
• Project & Timeline Management Track deliverables, maintain project timelines, and ensure timely completion of scientific and operational tasks.
• Presentation Development Build compelling PowerPoint decks for meetings, product discussions, and scientific communication.
• Process Documentation Develop workflows, and documentation that support scalable PV and product development processes.
• Quality & Compliance Awareness Maintain awareness of global PV guidelines (FDA, EMA, ICH) and ensure scientific content aligns with regulatory expectations.

Required Skills & Competencies

• Strong understanding of pharmacology, drug safety, and clinical concepts
• Ability to analyze scientific data and convert insights into actionable recommendations
• Excellent written communication and scientific writing skills
• Proficiency in PowerPoint, Excel, Power BI and data visualization tools
• Strong organizational skills with the ability to manage multiple priorities
• High attention to detail and commitment to accuracy

Preferred Qualifications

• Experience in PV, medical writing, regulatory affairs, or drug safety analytics
• Familiarity with safety databases, literature search tools, or PV workflows
• Prior internship or project experience in pharma, or biotech

What We Offer

• Highgrowth environment with rapid learning and accelerated career progression
• Flexible remote work culture
• A chance to build foundational systems in an earlystage company