IQVIA Fresher Jobs for B. Pharm, M. Pharm, or PharmD students: Centralized Monitoring Associate

• Introduction
• Job Overview
• Responsibilities
• Shift Timing and Location
• Mode of Work
• Eligibility Criteria
• Application Process
• Conclusion
• FAQs

IQVIA Fresher Jobs for B. Pharm, M. Pharm, or PharmD students: Centralized Monitoring Associate

Introduction

Are you a pharmacy graduate looking for an exciting career opportunity? IQVIA, a leading healthcare technology and services company, is currently hiring for the position of Centralized Monitoring Associate. This article provides all the essential information about the job, including educational qualifications, shift timing, location, mode of work, and eligibility criteria. If you are a fresher and a local candidate, this could be the perfect opportunity for you. Read on to learn more about this exciting career opportunity with IQVIA.

Job Overview

As a Centralized Monitoring Associate at IQVIA, you will play a crucial role in supporting clinical trials by ensuring compliance with protocols, regulatory requirements, and quality standards. Your primary responsibility will be to monitor trial data remotely and perform analysis to identify any potential risks or issues. You will work closely with cross-functional teams, including site monitors and project managers, to address any findings and ensure the successful execution of clinical trials.

Responsibilities

1. Remote Monitoring: Conduct remote monitoring of clinical trial data to identify trends, outliers, and potential risks, ensuring adherence to protocols and regulatory guidelines.
2. Data Analysis: Analyze trial data using statistical tools and techniques to identify patterns and detect any anomalies or deviations from expected outcomes.
3. Risk Assessment: Assess risks associated with the trial and identify areas that require additional monitoring or intervention.
4. Quality Control: Ensure the accuracy, integrity, and completeness of clinical trial data through regular quality checks and validations.
5. Issue Identification and Resolution: Identify issues or non-compliance with protocols and communicate them to the appropriate stakeholders for resolution.
6. Documentation and Reporting: Maintain accurate and up-to-date documentation of monitoring activities, findings, and actions taken. Generate reports and present findings to project teams as required.
7. Collaboration and Communication: Collaborate with site monitors, project managers, and other stakeholders to address any identified issues and ensure proper trial management.
8. Continuous Improvement: Contribute to process improvement initiatives by providing feedback and suggesting innovative approaches to enhance monitoring effectiveness and efficiency.

Shift Timing and Location

The shift timing for the Centralized Monitoring Associate position is from 02:00 PM to 11:00 PM. This afternoon shift allows for flexibility and can be suitable for individuals who prefer working during non-traditional hours. The job location is Mumbai (Thane) or Ahmedabad, providing opportunities in two vibrant cities known for their thriving pharmaceutical and healthcare industries.

Mode of Work

IQVIA requires Centralized Monitoring Associates to work from the office. This mode of work ensures effective collaboration and communication with the team members and facilitates seamless coordination of activities. Working from the office also provides access to necessary resources and infrastructure, enabling you to perform your duties efficiently and effectively.

Eligibility Criteria

To be eligible for the Centralized Monitoring Associate position at IQVIA, you must meet the following criteria:

• Possess a B. Pharm, M. Pharm, or PharmD degree
• Be a fresher with no prior work experience
• Be a local candidate residing in Mumbai (Thane) or Ahmedabad
• Have strong analytical and communication skills
• Exhibit attention to detail and the ability to work in a team environment

Application Process

If you meet the eligibility criteria and are interested in applying for the Centralized Monitoring Associate position at IQVIA, kindly share your updated resume to [email protected]. Ensure that your resume highlights your educational qualifications, relevant skills, and any additional information that showcases your potential as a valuable team member. The IQVIA recruitment team will review your application and contact you if your profile matches their requirements.

Conclusion

IQVIA’s hiring for the Centralized Monitoring Associate position presents an excellent opportunity for freshers in the pharmacy field to kick-start their careers in the healthcare industry. This role involves monitoring clinical trials, ensuring compliance, and contributing to the analysis of clinical trial data. With a focus on quality and regulatory standards, IQVIA offers a challenging and rewarding work environment. If you meet the eligibility criteria and are passionate about making a difference in the healthcare sector, don’t miss out on this exciting opportunity.

FAQs

1. What is the role of a Centralized Monitoring Associate at IQVIA? As a Centralized Monitoring Associate, your responsibilities include monitoring clinical trials, ensuring compliance with protocols, regulatory requirements, and quality standards, and assisting in the analysis of clinical trial data.