Are you looking for an exciting opportunity in pharmacovigilance? Caidya offers a role as a Pharmacovigilance Associate in Trivandrum, India. Whether you prefer working from home or at the office, this position provides flexibility while contributing to the vital field of patient safety and drug monitoring.
Company Introduction
Caidya is a trusted name in the healthcare and life sciences industry, dedicated to ensuring the highest standards of patient safety through innovative pharmacovigilance solutions. Our team collaborates globally to provide comprehensive safety monitoring for clinical trials and post-marketing surveillance. We are committed to compliance with ICH Guidelines, local regulations, and client-specific requirements.
Key Responsibilities
As a Pharmacovigilance Associate, you will:
- Manage Safety Data
- Retrieve SAE/AE-associated data from eCRF systems.
- Review source documents for redacting protected information.
- Enter SAE/AE information into the safety database.
- Upload documentation to systems like eTMF and Outlook folders.
- Support Reporting and Documentation
- Assist in creating pdf bundles for SAE information.
- Process requests for CIOMS/MedWatch forms.
- Maintain accurate project tracking.
- Assist in Safety Reporting
- Follow up on SAE/AE queries.
- Provide support for safety reporting processes.
- Collaboration and Team Support
- Work closely with PV Specialists and Team Leads.
- Participate in on-the-job training to stay updated on pharmacovigilance practices.
Qualifications
- Education: A degree in healthcare or life sciences is preferred.
- Experience: Prior experience in administrative tasks or computer applications is desirable.
Required Skills
- Strong written and verbal communication skills in English.
- Proficiency in Microsoft Office applications.
- Attention to detail and organizational skills.
- Knowledge of pharmacovigilance, ICH GCP guidelines, and regulatory requirements (preferred).
- Ability to adapt to a dynamic environment with honesty, trust, and flexibility.
