Intake, process, and assess adverse event reports according to regulatory requirements.
Conduct case triage and data entry into safety databases with high accuracy.
Ensure compliance with regulatory timelines and SOPs to maintain quality standards.
Assist in literature surveillance and medical review support to stay updated on industry trends.
Collaborate with cross-functional teams to achieve organizational goals.
Develop and implement processes to improve pharmacovigilance activities.

Job Requirements

Strong understanding of pharmacology and adverse drug reactions is essential.
Excellent written and verbal communication skills are needed for effective collaboration.
Attention to detail and accuracy are crucial for high-quality work.
Eagerness to learn and grow within the PV domain demonstrates a commitment to professional development.
Ability to work in a fast-paced environment and meet deadlines is required.
Familiarity with regulatory requirements and industry standards is preferred.
Qualification: M.S., M.Pharm, BDS, or MDS.

About Company

CONTINUUM India is a leading player in the pharmacovigilance industry, committed to delivering high-quality services and solutions. We offer a dynamic and supportive work environment, with opportunities for growth and development.

How to Apply

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Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

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