Veeda Lifesciences Walk-in Interview 2025.Veeda Lifesciences Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..
Vacancy details:
Important Details :
Job Description: Greetings from Veeda Lifesciences..!!
Job Responsibilities:
1-Aggregate Reports:
* Collect safety data and prepare Risk Management Plans (RMP), PBRERs/PSURs, PADERs, and addendums to clinical overview summaries.
* Collaborate with cross-functional teams to resolve issues during safety data review and report preparation.
* Ensure timely submission of reports to meet regulatory compliance.
2-Literature Search & Review:
* Set up search strategies and monitor literature databases for relevant safety information.
* Perform initial review of literature articles, segregating them into ICSRs, AOIs, and other relevant categories.
3-Triaging & Case Processing, Quality Check:
* Receive, track, and triage Individual Case Safety Reports (ICSRs).
* Conduct duplicate searches and ensure case processing aligns with SOPs.
* Review case quality against source documents.
4-Medical Inquiry Management:
* Handle Medical Information Contact Center (MICC) activities.
* Respond to medical, pharmaceutical, and technical inquiries, including adverse events (AEs).
* Maintain records and ensure timely responses to inquiries.
* Report adverse events to the case processing team.
Required Skills:
Knowledge of pharmacovigilance principles and regulatory guidelines.
Familiarity with safety databases and literature search tools.
Strong analytical and problem-solving skills.
Excellent communication and documentation skills.
Interested Candidates can share their resumes at Vaibhav.D3662@veedalifesciences.com or on 6359600877.
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