Are you looking for a rewarding career in clinical operations? IQVIA, a global leader in healthcare intelligence and clinical research, is hiring for the position of Centralized Monitoring Assistant in Thāne, Mahārāshtra. This is a full-time role with an end date of 07/03/2025. If you have a background in life sciences and a passion for contributing to innovative medical research, this could be the perfect opportunity for you. Read on to learn more about the job responsibilities, qualifications, and how to apply.
Job Overview
As a Centralized Monitoring Assistant, you will provide essential project-related support to assigned clinical study teams. Your role will ensure that all work is conducted in compliance with standard operating procedures (SOPs), good clinical practices (GCP), and applicable regulatory requirements. You will also be responsible for meeting quality and timeline metrics, contributing to the successful execution of clinical trials.
Key Responsibilities
- Provide study-level administrative support to the clinical study management team, including preparing status reports, maintaining study trackers, and following up on outstanding issues.
- Assist in updating and maintaining systems within project timelines to ensure compliance and credible data for analysis.
- Prepare i-site packs for assigned studies by pulling relevant reports.
- Perform access management tasks, such as processing access requests and coordinating with vendors.
- Support Technical Solution Specialists (TSS) with Excel formulations and front-end tasks.
- Monitor site performance, identify risks, and recommend corrective actions.
- Review the effectiveness of recommended actions and escalate issues as needed.
- Attend Kick-Off meetings, weekly team meetings, and client meetings as required.
- Adhere to key activities outlined in the Statement of Work (SOW) as per customer requirements.
Qualifications
- Education: Graduate or Post Graduate in Life Sciences or equivalent.
- Experience: Minimum of 2 years of work experience, with at least 6 months of relevant experience in clinical operations or a related field.
- Knowledge: Basic understanding of regulatory requirements, including ICH-GCP and local guidelines.
- Skills:
- Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).
- Strong written and verbal communication skills in English.
- Effective time management and attention to detail.
- Ability to build and maintain relationships with coworkers, managers, and clients.
- Strong listening and phone skills.
- Good data entry skills.
About IQVIA
IQVIA is a trusted global provider of advanced analytics, technology solutions, and contract research services to the life sciences and healthcare industries. With a mission to accelerate the development and commercialization of innovative medical treatments, IQVIA plays a pivotal role in improving patient outcomes and population health worldwide.
