Live opening · Posted 2 days ago

Pharmacoviglence

Arm · Dharmapuri, Tamil Nadu, India (On-site)
Linkedin No
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At a glance

The key details from the original listing.

Posted 2 days ago
CompanyArm
LocationDharmapuri, Tamil Nadu, India (On-site)
Work modeNo
SourceLinkedin
Listed2 days ago

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About the role

Description supplied by the original job listing.

Company Description Sri Lakshmi Narayan College of Pharmacy in Dharmapuri is an emerging institution dedicated to pharmaceutical education, research, and professional development. The college focuses on preparing learners for careers across the pharmaceutical and healthcare sectors, with particular emphasis on safe and effective medication use. It aims to foster a culture of academic excellence, ethical practice, and community service. Faculty and staff collaborate to create a supportive environment for learning, innovation, and industry engagement. The institution is committed to building strong links with hospitals, industry, and regulatory bodies to enhance practical exposure and career opportunities.
Role Description The Pharmacovigilance professional will be responsible for monitoring, assessing, and documenting the safety of medicinal products used in clinical and educational settings. Day-to-day tasks include collecting and evaluating adverse drug reaction reports, maintaining accurate safety databases, and preparing concise safety summaries and regulatory documents. The role involves collaborating with faculty, clinical partners, and regulatory authorities to support drug safety reporting and compliance with national and international guidelines. The individual will also participate in training students and staff on pharmacovigilance processes, good documentation practices, and emerging safety signals. This is a full-time, on-site role located at Sri Lakshmi Narayan College of Pharmacy in Dharmapuri.
Qualifications
Strong knowledge of pharmacology, clinical pharmacy, and drug safety principles, with the ability to analyze adverse event data and identify potential safety concerns.
Proficiency in medical and scientific documentation, including case report preparation, safety narratives, and regulatory correspondence.
Familiarity with pharmacovigilance regulations, guidelines, and reporting requirements (e.g., national drug safety programs, international standards).
Competence in data collection and basic data analysis using standard office and database tools, with attention to accuracy and confidentiality.
Effective communication skills for collaborating with healthcare professionals, faculty, students, and regulatory stakeholders.
Ability to work systematically, manage multiple cases or projects, and maintain detailed records in a time-bound environment.
Bachelor’s or Master’s degree in Pharmacy or a related pharmaceutical discipline; specialized training or certification in pharmacovigilance is an advantage.
Prior experience or internship in pharmacovigilance, clinical research, or drug safety is preferred but motivated early-career professionals may also be considered.

Work arrangement
No

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