WhatsApp Group
Join
WhatsApp Channel
Join
Telegram Group
Join
Ad

Myriad Consulting Hiring For Pharmacovigilance Case Processing

Published on

Myriad Consulting

B.Pharm / M.Pharm / Pharm.D / B.Sc / M.Sc Life Sciences

₹4 LPA

Mumbai & Bangalore

1–4 years

Verified Job

Email Application

Why Use Pharmabharat?

Real-Time Job Alerts

Trusted by Top Pharma Employers

Exclusive Pharma Industry Insights

Verified & Trusted Listings

Ad

Myriad Consulting has announced a new hiring opportunity for Pharmacovigilance (PV) Case Processing professionals in Mumbai and Bangalore. Candidates with 1 to 4 years of experience in Safety Case Processing and hands-on knowledge of Veeva Safety and Oracle Argus can apply for this opportunity.

The position is suitable for experienced pharmacovigilance professionals looking to strengthen their careers in drug safety, ICSR processing, and safety database operations. Selected candidates will be required to work from the office.

Myriad Consulting PV Case Processing Job Overview

  • Company: Myriad Consulting
  • Role: PV – Case Processing
  • Department: Pharmacovigilance / Drug Safety
  • Location: Mumbai & Bangalore
  • Work Mode: Work From Office (WFO)
  • Experience: 1–4 years in Safety Case Processing
  • Required Tools: Veeva Safety and Oracle Argus
  • Current CTC Requirement: Below ₹4 LPA
  • Interview Mode: Virtual
  • Interview: Saturday
  • Notice Period: Candidates who can join within approximately 30–40 days after accepting the offer are preferred.

Key Responsibilities

Candidates selected for the PV Case Processing job may be responsible for activities associated with pharmacovigilance case management and drug safety operations, including:

  • Processing Individual Case Safety Reports (ICSRs) in accordance with applicable procedures and timelines.
  • Reviewing safety information received from various sources for completeness and accuracy.
  • Performing case data entry and maintaining accurate information in safety databases.
  • Working with Veeva Safety and Oracle Argus for pharmacovigilance case processing activities.
  • Supporting adverse event and serious adverse event case management.
  • Performing case quality checks and identifying missing or inconsistent safety information.
  • Supporting follow-up activities when additional information is required.
  • Maintaining case documentation according to organizational SOPs and pharmacovigilance requirements.
  • Ensuring cases are processed within applicable regulatory and internal timelines.
  • Supporting overall compliance and quality requirements within pharmacovigilance operations.

Specific responsibilities may vary depending on the project, client requirements, and assigned PV process.

Qualifications and Eligibility

The hiring notice specifies experience requirements but does not state a particular educational qualification. Candidates from Pharmacy, Life Sciences, Clinical Research, Biotechnology, Microbiology, Biochemistry, Nursing, Medical or related healthcare/life-science backgrounds may be considered where their education and professional experience meet the employer’s requirements.

Applicants should have:

  • 1–4 years of Safety Case Processing experience in Pharmacovigilance
  • Practical exposure to Veeva Safety
  • Practical exposure to Oracle Argus
  • Understanding of pharmacovigilance and drug safety case-processing workflows
  • Knowledge of ICSR processing and safety data management
  • Ability to work from the Mumbai or Bangalore office
  • Current CTC below ₹4 LPA, as specified in the hiring announcement
  • Ability to join within approximately 30–40 days after offer acceptance

Candidates should verify educational eligibility directly with the recruiter because a specific degree requirement was not included in the provided hiring announcement.

Why Consider This PV Opportunity?

This opening can provide experienced drug safety professionals with exposure to widely used pharmacovigilance platforms such as Oracle Argus and Veeva Safety. Experience with established safety databases and end-to-end PV case processing can also strengthen a candidate’s profile for future roles in ICSR management, drug safety operations and pharmacovigilance.

Interview Details

The recruitment process includes a virtual interview scheduled for Saturday. Candidates planning to apply should keep their updated CV ready and review core pharmacovigilance concepts, including ICSR processing, seriousness, expectedness, causality, listedness, follow-up cases, duplicate checks, narratives, MedDRA coding and regulatory reporting timelines.

How to Apply

Interested candidates can send their updated CV directly to the recruiter:

Email: sandeep.dalvi@myriadconsulting.co.in

Ad

Share This Job

✅ Job Copied Successfully!