Location: Bengaluru, Karnataka, India | Job Type: Full-Time | Experience: 0–2 years
Job Category:
Pharmacovigilance / Drug Safety
Life Sciences / Clinical Operations
Entry-Level / Associate
About the Role:
Accenture is seeking a Pharmacovigilance Services Associate to join our Life Sciences R&D team in Bengaluru. In this role, you will support pharmacovigilance operations, monitoring the safety of pharmaceutical products to ensure patient safety and regulatory compliance. This position is ideal for early-career professionals with a background in pharmacy, looking to build a career in drug safety and pharmacovigilance.
As a Pharmacovigilance Services Associate, you will handle case identification, data entry, MedDRA coding, case processing, and follow-ups for Individual Case Safety Reports (ICSRs) in alignment with client guidelines and global regulatory requirements.
Key Responsibilities:
Monitor and assess the safety profile of pharmaceutical products, detecting and evaluating adverse effects.
Collect and analyze safety data from clinical trials, healthcare providers, and patients.
Create, manage, and submit ICSRs in the safety database according to global regulatory standards.
Apply MedDRA coding and ensure accurate case processing and follow-ups.
Resolve routine pharmacovigilance issues using standard guidelines and escalate complex cases to senior staff.
Maintain compliance with all applicable regulatory and client-specific requirements.
Work collaboratively within the pharmacovigilance team to support timely and accurate safety reporting.
Participate in rotational shifts as required by operational needs.
Qualifications & Experience:
Educational Requirements: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).
Experience: 0–2 years in pharmacovigilance, drug safety, clinical research, or related life sciences roles.
Knowledge of pharmacovigilance operations, adverse event reporting, and regulatory compliance is preferred.
Strong analytical, organizational, and attention-to-detail skills.
Ability to work independently and as part of a team in a fast-paced environment.
Skills & Competencies:
Understanding of pharmacovigilance guidelines and regulatory requirements.
Ability to perform accurate MedDRA coding and case data entry.
Strong communication and interpersonal skills.
Proficiency in Microsoft Office and the ability to learn internal safety databases.
Commitment to patient safety, compliance, and continuous learning.
Why Join Accenture:
Work with a global leader in digital, cloud, and life sciences services.
Gain hands-on experience in pharmacovigilance and clinical operations.
Be part of a collaborative, inclusive, and diverse workplace culture.
Access continuous learning opportunities, skill certifications, and career development programs.
Contribute to projects that impact global healthcare and patient outcomes.
Apply Now to launch your career in pharmacovigilance with Accenture in Bengaluru and be part of a team that ensures drug safety and enhances patient trust worldwide.
Gujarat :
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Baddi | Solan |Rajasthan :
Banasthali | Bhiwadi | Jaipur | Pilani | Udaipur |Karnataka :
Bangalore | Belgaum | Bengaluru | B.G Nagara | Bommasandra | Colorado | Czech Republic | Karnataka | Mangaluru | Mysore | Udupi |Punjab :
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Siliguri |Illinois :
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Koropi | Athens |Greece :
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Auckland |New Zealand :
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Croatia |Zagreb :
Zagreb |Estonia :
Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
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Midrand | South Africa |Nišava District :
Niš |Bohemia :
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