Pharmacovigilance Associate @ Techno Endura

Job Description

Responsibilities:

• Process and manage adverse event reports: This includes reviewing AE reports from healthcare professionals, patients, and other sources. They need to assess the seriousness of the event and determine whether it needs to be reported to regulatory authorities.
• Maintain safety databases: Pharmacovigilance Associates enter and maintain AE data in safety databases. This data is used to track trends and identify potential safety signals.
• Communicate with healthcare professionals: They may need to contact healthcare professionals to gather additional information about an AE or to provide them with safety updates.
• Prepare safety reports: Pharmacovigilance Associates prepare periodic safety reports for regulatory authorities. These reports summarize the safety data for a product and identify any potential safety concerns.
• Stay up-to-date on safety information: They need to keep up-to-date on the latest safety information about the products they are responsible for. This includes reading scientific literature, attending conferences, and participating in training programs.

Qualifications:

• 0- 2 Years Experience
• Bachelor's degree in life sciences, pharmacy, nursing, or a related field.
• Good understanding of Good Pharmacovigilance Practice (GVP) guidelines and regulations.
• Excellent communication, interpersonal, and organizational skills.
• Strong attention to detail and ability to multitask.
• Proficient in Ms Office Suite and safety database software.

Interested to apply can share Cv or call/whatsapp to hidden_mobile
 

Employement Category:

Employement Type: Full time
Industry: Medical / Healthcare
Role Category: Medical / Healthcare
Functional Area: Not Applicable
Role/Responsibilies: Pharmacovigilance Associate

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Keyskills:   adverse events monitoring drug safety pharmacovigilance adverse event reporting