Pharmacovigilance Services New Associate
Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 0–2 Years
Qualification: Bachelor of Pharmacy (B.Pharm)
Industry: Pharmacovigilance / Drug Safety / Life Sciences R&D
Job ID: AIOC-S01632879
About the Role
We are seeking a Pharmacovigilance Services New Associate to join a dynamic Life Sciences R&D team supporting global biopharmaceutical clients. This entry-level role is ideal for candidates looking to build a strong foundation in pharmacovigilance and drug safety. The position focuses on adverse event case processing, safety data management, and regulatory compliance, contributing to the safe and effective use of pharmaceutical products.
Key Responsibilities
Perform case identification, data entry, and processing of Individual Case Safety Reports (ICSRs) in the safety database as per client guidelines and global regulatory requirements. Conduct MedDRA coding and ensure accurate documentation of adverse events. Support case follow-ups, submissions, and lifecycle management of safety cases.
Analyze safety data from various sources including clinical trials, healthcare providers, and patient reports to support drug safety surveillance. Ensure all activities are performed in compliance with pharmacovigilance regulations and internal standard operating procedures. Maintain high standards of data quality, accuracy, and completeness in all assigned tasks.
Work closely with team members and supervisors to resolve routine issues based on established guidelines. Follow detailed instructions and contribute as an individual team member within a structured workflow. Participate in continuous learning and adapt to process updates and regulatory requirements. This role may require working in rotational shifts based on business needs.
Required Qualifications
Bachelor of Pharmacy (B.Pharm) is mandatory. Candidates with 0–2 years of experience or fresh graduates with relevant pharmacovigilance knowledge are encouraged to apply.
Key Skills and Competencies
Basic understanding of pharmacovigilance principles, adverse event reporting, and drug safety processes. Familiarity with MedDRA coding and safety databases is an advantage. Strong attention to detail with good analytical and problem-solving skills. Ability to follow processes, guidelines, and instructions accurately.
Good communication skills and the ability to work effectively within a team environment. Basic proficiency in computer applications and data entry tools. Willingness to learn, adapt, and grow in a fast-paced clinical and regulatory environment.
About the Organization
The organization is a global leader in professional services with strong capabilities in life sciences, digital transformation, and technology-driven operations. Through its Life Sciences R&D vertical, it supports pharmaceutical and biotechnology companies across clinical development, regulatory services, pharmacovigilance, and patient-centric solutions. The company combines scientific expertise with advanced technology to improve patient outcomes and accelerate innovation.
Work Environment and Benefits
Employees gain exposure to global projects, structured training programs, and career development opportunities in pharmacovigilance and life sciences. The organization promotes a collaborative and inclusive work culture, encouraging continuous learning and professional growth.
How to Apply
Interested candidates can apply through the official careers portal to start their career in pharmacovigilance and drug safety.
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