Pharmacovigilance – Case Processing Executive (Life Sciences Fresher)

2COMS Consulting Pvt. Ltd.; Bengaluru; On-site; INR 237,000 - 321,000; Full time

Job summary

2COMS Consulting Pvt. Ltd. in Bangalore invites Life Sciences freshers to join as Pharmacovigilance / Drug Safety Case Processing Executives. This contract-to-hire opportunity places you on the client payroll after 6 months, with shifts from 6:00 AM to 3:00 PM or 3:00 PM to 12:00 AM.

You will handle case creation, data entry, and follow-up in global safety databases, ensuring compliance with SOPs and regulatory standards while developing pharmacovigilance knowledge on international accounts.

Qualifications

• Attention to detail and documentation skills required for case processing.
• Basic understanding of drug safety and adverse event reporting.
• Willingness to work in rotational shifts and fast-paced processes.

Responsibilities

• Identify and create cases in the global safety database from intake sources.
• Retrieve and follow up on safety information as per SOPs and regs.
• Triage safety cases and ensure accurate data entry in core safety databases.
• Submit and follow up cases in line with client guidelines and standards.
• Maintain adherence to pharmacovigilance processes and quality benchmarks.

Skills

Attention to detail

Documentation skills

Drug safety knowledge

Pharmacovigilance concepts

Communication skills

Education

B.Pharm

M.Pharm

Pharm D

Job description

Pharmacovigilance – Case Processing Executive (Life Sciences Fresher)

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Job Description

Pharmacovigilance – Case Processing Executive (Life Sciences Fresher)

Employment Type: Contract to Hire (6 Months)

Payroll: 2COMS

About the Role

We are hiring Life Sciences freshers for a Pharmacovigilance / Drug Safety role with our reputed MNC client based in Bangalore. This is a Contract-to-Hire opportunity where selected candidates will work with the client while being on 2COMS payroll for the initial 6 months.

Shift Timing

6:00 AM – 3:00 PM

3:00 PM – 12:00 AM

(Candidates must be flexible to work in any shift)

Key Responsibilities

Identification and creation of cases in the Global Safety Database from reports received via intake workflow, client mailbox, electronic gateway, and other applicable sources.

Retrieval of new incoming safety information and follow-up correspondence for existing cases as per client SOPs and global regulatory requirements.

Triage and prioritization of safety cases (serious & non-serious).

Accurate data entry and case processing in core safety databases.

Submission and follow-up of cases in compliance with client guidelines and global regulatory standards.

Ensure adherence to pharmacovigilance processes and quality benchmarks.

Requirements

What We’re Looking For

Attention to detail and strong documentation skills

Basic understanding of drug safety / adverse event reporting

Ability to work in a structured, process-driven environment

Immediate joiners preferred

Eligibility Criteria

B.Pharm

M.Pharm

Pharm D

Strong understanding of pharmacovigilance concepts preferred

Good written and verbal communication skills

Willingness to work in rotational shifts

CTC-25000 (Including PF and Accidental Insurance)

Chance to get into the direct payroll of the client

Chance to work with international clients