IQVIA Hiring Regulatory Affairs Specialist (Pharmacovigilance)

IQVIA Hiring Regulatory Affairs Specialist

IQVIA, a global leader in advanced analytics, technology solutions, and clinical research services to the life sciences industry, is seeking a Regulatory Affairs Specialist to join their team in Mumbai, Maharashtra. This is a full-time position offering an exciting opportunity for professionals with experience in Pharmacovigilance or Regulatory Affairs to make a significant impact in the field of drug safety and regulatory compliance.

Job Responsibilities

As a Regulatory Affairs Specialist, you will be responsible for managing and maintaining drug safety data in the European Medicines Agency’s EudraVigilance database. Your key responsibilities will include:

Job Description of a XeVMPD Associate:

Data Management: Responsible for entering and updating information about medicinal products in the XeVMPD system in accordance with EU regulatory guidelines.

Quality Assurance: Ensures the accuracy and quality of data entered into the system. Regularly reviews and cleans data to maintain its integrity.

Regulatory Compliance: Ensures compliance with all relevant regulatory guidelines related to XeVMPD. Keeps up-to-date with changes in regulations and implements them in data management practices.

Collaboration: Works closely with other departments, such as Regulatory Affairs and Pharmacovigilance, to collect necessary information and ensure its correct entry into the system.

Reporting: Generates regular reports on data management activities and presents findings to relevant stakeholders.

Training: May be responsible for training other team members on XeVMPD data entry and management practices.

Problem Solving: Addresses and resolves any issues or discrepancies in the XeVMPD data promptly.

Requirements for this role typically include a degree in Pharmacy, Life Sciences, or a related field, along with experience in Pharmacovigilance or Regulatory Affairs. Strong attention to detail, knowledge of EU regulations related to drug safety, and proficiency in data management systems are also essential.

Qualifications

To be considered for this role, you should have:

• A degree in Pharmacy, Life Sciences, or a related field.
• Experience in Pharmacovigilance or Regulatory Affairs.
• Strong attention to detail.
• Knowledge of EU regulations related to drug safety.
• Proficiency in data management systems.

Requirements for this role typically include a degree in Pharmacy, Life Sciences, or a related field, along with experience in Pharmacovigilance or Regulatory Affairs. Strong attention to detail, knowledge of EU regulations related to drug safety, and proficiency in data management systems are also essential.

How to Apply

If you meet the qualifications and are excited about the opportunity to work with a global leader in the life sciences industry, we encourage you to apply online through the following link: IQVIA Application Portal.