Pharmacovigilance Services New Associate

Accenture 4.9

1–3 Years | Salary Not Disclosed | Chennai
Full Time
Posted: 06 May 2026 Applicants: 0

Pharmacist (Retail/Hospital)

Onsite

3

Any

Not Required

No

Job Description

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services New Associate
Qualifications:Bachelor of Pharmacy/Bachelor Degree in Life Sciences
Years of Experience:0 to 1 years

Our 784,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. What would you do?
You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world¢?
s leading biopharma companies bring their vision to life ¢??? enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients. The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications.Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.
What are we looking for?
Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients. The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications.Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients. The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications.

Roles and Responsibilities:
In this role you are required to solve routine problems, largely through precedent and referral to general guidelines
Your primary interaction is within your own team and your direct supervisor
In this role you will be given detailed instructions on all tasks
The decisions that you make impact your own work and are closely supervised
You will be an individual contributor as a part of a team with a predetermined, narrow scope of work
Please note that this role may require you to work in rotational shifts

Qualification
Bachelor of Pharmacy,Bachelor Degree in Life Sciences
Role: Clinical Informatics
Industry Type: IT Services & Consulting
Department: Healthcare & Life Sciences
Employment Type: Full Time, Permanent
Role Category: Health Informatics

Qualifications

UG: B.Pharma in Pharmaceutical Analysis and Quality Assurance, Any Graduate
PG: Any Postgraduate

Key Skills

pharmacovigilance cloud r pharmaceutical operations drug safety pharmacy clinical trials life sciences data entry research healthcare
Deadline: 30 Jun 2026

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