Associate Clinical Data Manager

IQVIA; Bloemfontein; On-site; ZAR 700,000 - 1,100,000; Full time

Job summary

IQVIA is seeking a Lead Data Manager to drive data management projects per sponsor requirements and deliver high-quality data products. You will coordinate with sites, departments and sponsors, oversee study meetings and audits, and ensure timely, accurate data delivery.

The role requires strong English communication, a science or pharmacy background, and advanced data handling skills. You will lead database setup and validation, support device integration validation, and guide training for new

Qualifications

• Degree in science or pharmacy or equivalent required.
• Excellent written and spoken English.
• Proficiency in data management concepts and processes.

Responsibilities

• Lead data management projects per sponsor requirements.
• Coordinate with departments, sites and sponsors as needed.
• Set up and validate databases for study data collection.
• Validate device integrations and ensure data quality.
• Monitor project progress, risks and corrective actions.
• Support training for new joiners and audits.

Skills

English fluency

Data management

Communication

Education

Master’s Degree / Post Graduate Science or Bachelor Pharmacy

Tools

Microsoft Excel

Job description

Job Overview

Acts as Lead Data Manager leading various data management projects as per sponsor requirements and to provide efficient, quality products. Support coordinate with other departments, sites and sponsors as and when necessary.

Essential Functions

• Gather Study Set up requirements through discussion and communication with relevant stakeholders.
• Perform Database Set up and validation to ensure quality study design for data collection.
• Support validation of new Device integrations.
• Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
• Ensure that all the deliverables are of expected quality standards and meet customer expectations.
• Support Training of New joiners.
• Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
• Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended by DTL.
• Manage the development and implementation of new technology / database revisions.
• Work closely with the programming team for process innovation and automation.
• Be compliant to trainings and eSOP reading.
• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
• Communication with Line Manager, Leadership and other team members across functions should be collaborative.

Qualifications

• Master’s Degree Post Graduate Science/Bachelor Pharmacy or equivalent
• English Fluency Spoken and English
• Advanced computer applications like Microsoft excel, word, Inbox etc
• Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process

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.