Arco Labs Hiring for Pharmacovigilance Department

Arco Labs Hiring for Pharmacovigilance Department: Literature/Regulatory Case Processing and Reviewing

Arco Labs, a leading pharmaceutical company, is currently seeking skilled professionals to join their Pharmacovigilance department. We have exciting opportunities for individuals with experience in literature and regulatory case processing and reviewing. These roles are based in Bangalore and offer a dynamic and challenging work environment.

Job Overview

Company Name: Arco Labs
Location: Bangalore
Department: Pharmacovigilance
Experience Level: 1 to 5 years
Mode of Work: Office-based

Open Position: ICSR-Data Entry Associate

Job Title: ICSR-Data Entry Associate
Qualification: M-Pharma, PharmD, B-Pharm
Experience: 1 to 3 years

As an ICSR-Data Entry Associate, you will be responsible for:

• Data Entry: Accurate and timely entry of Individual Case Safety Reports (ICSR) into the safety database.
• Quality Review: Ensuring high-quality data entry and adherence to regulatory guidelines.
• Case Processing: Handling and processing of pharmacovigilance cases including literature cases.
• Regulatory Compliance: Maintaining compliance with global regulatory requirements and company standards.

Key Responsibilities

• Literature Review: Conducting thorough reviews of medical literature to identify and extract relevant safety information.
• Case Processing: Managing and processing regulatory and literature cases in accordance with standard operating procedures (SOPs).
• Data Quality: Ensuring the accuracy and completeness of safety data entered into the database.
• Collaboration: Working closely with cross-functional teams to ensure efficient case processing and timely reporting.
• Regulatory Submissions: Assisting in the preparation and submission of regulatory reports and safety summaries.

Qualifications and Experience

• A degree in M-Pharma, PharmD, or B-Pharm.
• 1 to 3 years of experience in pharmacovigilance, specifically in ICSR data entry and case processing.
• Strong attention to detail and excellent data management skills.
• Familiarity with global regulatory requirements and pharmacovigilance practices.

How to Apply

If you are interested in this exciting opportunity and meet the qualifications, please share your CV with us at Dev.kiran@arcolab.com