Pharmacovigilance Associate Hiring at Caidya – Home/Office-Based

Are you looking to build a rewarding career in pharmacovigilance? Caidya, a globally renowned clinical research organization, is hiring Pharmacovigilance Associates. Whether you prefer to work from the comfort of your home or the corporate office in Trivandrum, this role offers flexibility, growth, and a chance to be part of a dynamic team.

Position Overview

• Job Title: Pharmacovigilance Associate
• Location: Trivandrum, India | Home/Office-Based
• Experience Required: Prior work experience preferred, but freshers with relevant qualifications are welcome
• Education Qualification: Degree in Healthcare or Life Sciences (preferred)

Job Responsibilities

As a Pharmacovigilance Associate, you will be responsible for ensuring the safety and regulatory compliance of clinical trials. Key responsibilities include:

• Works under the supervision of PV Specialists and Team Lead
• Checks study mailboxes and retrieves SAE/AE-associated source data from eCRF system, as requested
• Reviews SAE/AE-associated source data for identification and redaction of any protected information
• Enters initial and follow up SAE information in the Caidya safety database or client’s database, according to project requirements, as required
• Uploads SAE/AE notifications, source documentation, acknowledgements, etc.  to designated systems including Outlook mail folders, the safety database and the eTMF, as required
• May assist with pdf bundle creation containing SAE information for designated studies
• May assist with processing of requests to create CIOMS/MedWatch forms from TEMPO Safety
• Ensures project tracking is kept current and complete for designated projects
• Provides assistance with safety reporting, as requested
• May assist with follow-up of outstanding SAE/AE queries, as needed
• Other duties as assigned by Team Lead and/or PV Specialists

Skills and Competencies

• Technical Skills:
  • Proficiency in Microsoft Office applications.
  • Familiarity with safety databases and eCRF systems.
• Soft Skills:
  • Strong written and verbal English communication.
  • Excellent organizational skills and attention to detail.
  • Team-oriented mindset with strong interpersonal skills.
• Regulatory Knowledge:
  • Basic understanding of ICH-GCP guidelines and pharmacovigilance documentation practices.

Application Process

Ready to make a difference in clinical safety and compliance? Apply today!

📧 Apply Here: Caidya Careers Portal