Pharmacovigilance QA Jr Auditor jobs: Veeda Clinical Research Ltd

Veeda Clinical Research Ltd as PV_QA_Jr Auditor

Are you an experienced professional in the field of pharmacovigilance and quality assurance? Veeda Clinical Research Ltd is actively seeking a talented individual to fill the position of PV_QA_Jr Auditor. If you have 1-2 years of experience and are passionate about ensuring safety and quality in clinical research, this could be the opportunity for you.

Introduction

In the world of clinical research, pharmacovigilance and quality assurance play an indispensable role in maintaining the safety and integrity of research activities. If you’re a dedicated professional looking to contribute to this critical aspect, Veeda Clinical Research Ltd has a position that aligns with your expertise.

About Veeda Clinical Research Ltd

Veeda Clinical Research Ltd is a prominent name in the clinical research domain, committed to conducting research that adheres to the highest standards of safety and quality. Our mission is to advance medical knowledge while prioritizing patient well-being.

Position Details

As a PV_QA_Jr Auditor, you will be entrusted with responsibilities that ensure the highest standards of safety, quality, and compliance in clinical research. Here’s what the position entails:

• Position: PV_QA_Jr Auditor
• Experience: We’re seeking candidates with 1-2 years of experience in the field.
• Location: The position is based in Ahmedabad.

Roles and Responsibilities

In this role, your responsibilities will encompass a wide range of tasks to uphold safety and quality in clinical research:

• Safety Report Review: You will review Individual Case Safety Reports (ICSRs), periodic safety updates reports, addendum to clinical overviews, Periodic Adverse Drug Experience Reports, and more.
• Quality Assurance: Review of Medical review, Quality review, Medical Enquiries, Pharmacovigilance Management Plan, Safety Data Exchange Agreement, and other processes.
• Compliance and Audit: Conduct system audits and vendor audits related to pharmacovigilance activities. Prepare for and address sponsor and regulatory inspections and queries.
• Signal Detection and Management: Participate in signal detection, evaluation, and management of authorized medicinal products.

Qualifications and Requirements

We are looking for candidates who possess the following:

• 1-2 years of relevant experience in pharmacovigilance and quality assurance.
• Understanding of database structures for pharmacovigilance activities.
• Strong knowledge of pharmacovigilance processes and regulatory guidelines.
• Excellent communication skills to interact with internal teams, vendors, sponsors, and regulatory authorities.

Application Process

If you’re ready to take your career in pharmacovigilance and quality assurance to the next level, we encourage you to share your resume with us at dhonisha.s2315@veedacr.com