Safetypulse247 has announced an opening for a Pharmacovigilance Scientist for a remote, full-time position. This opportunity is particularly relevant for B.Pharm graduates interested in pharmacovigilance, drug safety, scientific writing, safety data analytics, and regulatory science.
Unlike a conventional pharmacovigilance operations position focused primarily on ICSR processing, this role combines safety data evaluation, scientific content development, data visualization, Power BI, project management, and cross-functional product support.
Candidates with approximately one year of relevant experience are preferred, while six months of internship or project experience in pharmacovigilance, pharma, biotechnology, medical writing, or related areas may also be considered.
For candidates looking for a remote pharmacovigilance job for B.Pharm graduates, this position provides exposure to both drug safety science and analytical/product-development activities within an early-stage US startup environment.
Key Responsibilities
Selected candidates for the Pharmacovigilance Scientist remote job will contribute to scientific, analytical, and product-development activities, including:
- Review, interpret, evaluate, and summarize drug safety data, scientific literature, clinical information, and other safety-related evidence.
- Support safety evaluations relevant to product development and regulatory strategy.
- Prepare high-quality scientific documents, reports, summaries, presentations, and other scientific communication materials.
- Analyze scientific and safety information and convert findings into meaningful insights and recommendations.
- Develop charts, graphs, dashboards, and visual summaries for communicating complex scientific information.
- Use tools such as Microsoft Excel and Power BI for data analysis and visualization.
- Collaborate with product engineering and other cross-functional stakeholders to align scientific findings with product strategy.
- Track project deliverables and maintain timelines for scientific and operational activities.
- Develop professional PowerPoint presentations for meetings, product discussions, and scientific communication.
- Create workflows, process documentation, and supporting materials for scalable pharmacovigilance and product-development processes.
- Maintain awareness of applicable global pharmacovigilance requirements and guidance, including FDA, EMA, and ICH expectations.
- Ensure scientific deliverables are accurate, consistent, appropriately documented, and aligned with applicable regulatory expectations.
Eligibility & Qualifications
Candidates interested in the Safetypulse247 Pharmacovigilance Scientist vacancy should meet the following requirements:
Mandatory Qualification
- Bachelor of Pharmacy (B.Pharm) is mandatory.
Experience
- Approximately 1 year of relevant experience is preferred.
- Candidates with 6 months of internship or project experience may also be considered.
- The job listing indicates an overall experience range of 0–3 years.
Relevant exposure may include:
- Pharmacovigilance
- Drug Safety
- Clinical Research
- Medical Writing
- Regulatory Affairs
- Drug Safety Analytics
- Pharmaceutical or biotechnology projects
Required Skills
Candidates should have a strong foundation in:
- Pharmacovigilance
- Drug Safety
- Pharmacology
- Clinical concepts
- Scientific data analysis
- Scientific writing
- Literature review
- Microsoft Excel
- Microsoft PowerPoint
- Power BI
- Data visualization
- MS Office
- Project management
- Scientific communication
- Attention to detail
Knowledge or familiarity with Argus, safety databases, literature-search tools, and pharmacovigilance workflows can be beneficial.
Pharmacovigilance & Regulatory Knowledge
Applicants should preferably understand the basic principles of:
- Adverse Event and Serious Adverse Event concepts
- Pharmacovigilance and drug safety
- Clinical safety information
- Scientific literature assessment
- Safety data evaluation
- Global pharmacovigilance guidelines
- FDA pharmacovigilance expectations
- EMA pharmacovigilance requirements
- ICH guidelines
- Safety databases and PV workflows
- Scientific and regulatory documentation
The position is broader than a standard case-processing role and requires candidates to combine scientific reasoning with analytical and business-oriented problem solving.
Preferred Qualifications
Safetypulse247 prefers candidates who have:
- Previous exposure to pharmacovigilance, medical writing, regulatory affairs, or drug safety analytics.
- Familiarity with pharmacovigilance safety databases.
- Knowledge of literature-search tools.
- Understanding of standard PV workflows.
- Internship or project experience within the pharmaceutical or biotechnology sector.
- Strong scientific presentation and communication skills.
- Ability to interpret data and communicate insights effectively.
Why This Role Is Different
The Pharmacovigilance Scientist position at Safetypulse247 is not described as a traditional PV operations role.
The position combines several functional areas:
Pharmacovigilance + Scientific Writing + Data Analytics + Power BI + Product Development
Candidates may therefore gain exposure beyond routine drug safety operations, particularly in scientific content development, visualization of safety information, product strategy, process development, and cross-functional collaboration.
This may be useful for early-career B.Pharm professionals who want to develop broader capabilities across pharmacovigilance science and healthcare analytics.
What Safetypulse247 Offers
According to the job posting, selected candidates can expect:
- Remote working opportunity
- Full-time permanent employment
- High-growth startup environment
- Rapid learning opportunities
- Exposure to scientific and product-development activities
- Cross-functional collaboration
- Opportunity to help develop foundational systems and processes
- Potential for increased responsibilities based on performance
- Accelerated career-development opportunities for strong performers
Salary
The advertised salary range for the Pharmacovigilance Scientist position is:
₹1,00,000 – ₹2,50,000 per year
Final compensation may depend on the candidate’s qualifications, relevant experience, internship/project exposure, and skills.
Who Should Apply?
This opportunity may be particularly suitable for:
- B.Pharm graduates seeking pharmacovigilance opportunities
- Early-career pharmacovigilance professionals
- Candidates with PV internship experience
- Candidates with drug safety projects
- B.Pharm graduates with strong pharmacology knowledge
- Candidates interested in scientific writing and safety analytics
- Candidates with Excel and Power BI skills
- Candidates interested in working with an early-stage startup
- Candidates seeking remote pharmacovigilance jobs
How to Apply
