Lab Cent Project Coordinator 1

IQVIA; Ernakulam; On-site; INR 320,000 - 520,000; Full time

Job summary

IQVIA in Kerala is seeking a Monitoring Associate to manage assigned monitoring responsibilities for simple protocols and non-protocol tasks with quality and timeliness. You will complete role-specific trainings and maintain regulatory documentation while supporting site activities.

The role requires a High School Diploma or equivalent and up to 1 year experience, strong English communication, and the ability to work in a fast-paced environment.

Qualifications

• High School Diploma or equivalent required.
• 0 to 1 year of experience.
• Basic knowledge of systems and procedures.
• Ability to handle multiple tasks.
• Strong written and verbal English communication.
• Experience in fast-paced, high-stress environments desirable.

Responsibilities

• Manage centralized monitoring activities for assigned projects.
• Complete role-specific trainings and assessments.
• Provision access for Infosario Portal.
• Ensure timely documentation for regulatory dossiers.
• Monitor timely release of patient laboratory reports.
• Maintain audit-ready documentation for monitoring activities.
• Participate in process-improvement initiatives.

Skills

Strong written and verbal English

Multi-tasking

Critical thinking

Problem solving

Communication

Education

High School Diploma or equivalent

Tools

Infosario Portal

Job description

Job Overview

Managing assigned monitoring responsibilities (simple protocols/ non-protocol tasks) competently, in a timely manner and with quality.

Job Overview

Managing assigned monitoring responsibilities (simple protocols/ non-protocol tasks) competently, in a timely manner and with quality.

Essential Functions

• Under minimal supervision perform centralized monitoring activities for the assigned projects which includes but is not limited to
• On time completion of assigned role specific trainings (self-learning courses, instructor led training, acknowledgement of e-SOP/WI etc.) and related assessment Loading and updating the active databases with details of participating sites
• Provisioning of access for Infosario Portal.
• Ensuring on-time completion of documentation(s) that form a part of the regulatory dossier for kit shipment [Kit Contents Chart(KCC)/Packing List//Import Permit].
• Monitoring on-time release of patient laboratory report by following up on the associated pending activity(ies) with related team(s).
• Ensuring that documentation is available for all monitoring activities performed for real-time audit readiness
• Participation in department/process improvement initiatives as applicable.

Qualifications

• High School Diploma or equivalent Req
• 0 to 1 year.
• Requires basic job knowledge of systems and procedures obtained through prior work experience or education.
• Must be able to comply with all applicable standards as required by the company.
• Demonstrated ability to handle multiple tasks.
• Demonstrated ability of critical thinking and problem solving.
• Strong written and verbal communication skills including good command of English language.
• Strong interpersonal, communication, organizational, and time management skills.
• Computer proficiency in word processing and spreadsheet applications.
• Demonstrated ability to work in a fast-paced, high stress environment highly desirable.
• Ability to establish and maintain effective working relationships with coworkers and managers.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.