Senior Drug Safety Associate at Soterius Noida | Clinical Safety & PV | 2–4 Yrs | Apply Online Keka 162949
Senior Drug Safety Associate at Soterius Noida | Clinical Safety & PV | 2–4 Yrs | Apply Online Keka 162949

Senior Drug Safety Associate Position at Soterius, Noida

A rare chance has emerged for aspiring professionals seeking a Senior Drug Safety Associate role in Clinical Safety and Pharmacovigilance. Soterius, located in Noida, is seeking a Senior Drug Safety Associate with 2–4 years of experience in drug safety and pharmacovigilance. Interested candidates are encouraged to apply online before the deadline.

About Soterius

Soterius is a prominent organization operating in the pharmaceutical sector, focusing on drug safety and pharmacovigilance. Based in Noida, Uttar Pradesh, Soterius is dedicated to ensuring the highest standards of safety and compliance in the drug development process. The company plays a crucial role in monitoring adverse drug reactions and maintaining regulatory compliance in clinical trials and post-marketing scenarios.

Job Details:

Company: Soterius

Job Title: Senior Drug Safety Associate

Experience: 2–4 Years

Location: Noida, Uttar Pradesh

Employment Type: Full-Time

Function: Clinical Safety and Pharmacovigilance

Posted On: 25 September 2026

Reference ID: 162949

Job Description

The Senior Drug Safety Associate will support drug safety and pharmacovigilance activities, including processing and reviewing adverse drug reactions, ICSR case processing, regulatory compliance, project ownership, quality management, and safety-related documentation. This role is pivotal in ensuring that all safety protocols are adhered to and that the highest standards of quality are maintained.

Drug Safety Associate Responsibilities

  • Support drug safety and pharmacovigilance activities as requested by management.
  • Record and review adverse drug reactions in safety or other relevant databases for post-marketing and clinical trial reports.
  • Ensure adverse event processing meets applicable regulatory standards and client procedures with high accuracy and quality.
  • Support development and deployment of assigned technology solutions, including implementation, validation, upgrades, bug fixes, change requests, and product lifecycle support.
  • Coordinate with required internal and external stakeholders.
  • Take ownership of assigned projects and tasks while maintaining timelines and quality.
  • Manage quality, compliance, and documentation across assigned projects.
  • Train and mentor personnel as required.

Eligibility Criteria

  • 2–4 years of experience in drug safety and pharmacovigilance activities.
  • Experience with adverse drug reaction recording and review.
  • Experience with ICSR case processing and compliance activities.

Required Skills

  • Drug Safety
  • Pharmacovigilance
  • Adverse Drug Reaction processing
  • ICSR case processing
  • Safety database operations
  • Regulatory compliance
  • Quality and documentation management
  • Project ownership and timeline management

How to Apply

Interested candidates can apply for the position through the following link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Conclusion

This is an excellent opportunity for qualified candidates to join Soterius as a Senior Drug Safety Associate. With a focus on drug safety and pharmacovigilance, the role promises a challenging and rewarding career path. Candidates are encouraged to apply at the earliest to secure their chance for this vital position.

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