Health Science Job: Data Team Lead at IQVIA – Bengaluru
Looking for a promising health science job in the clinical research industry? IQVIA is hiring a Data Team Lead in Bengaluru, India. This hybrid, full-time opportunity is ideal for professionals with experience in clinical data management who want to grow their careers with a global leader in healthcare intelligence and life sciences.
Job details:
- Job Position: Data Team Lead (DTL)
- Location: Bengaluru, India
- Job ID: R1511951
About the Company:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company creates intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Professionals exploring IQVIA careers gain exposure to global clinical research projects, advanced healthcare analytics, and cutting-edge technologies in drug development.
Job Overview:
This health science job involves managing end-to-end delivery of data management services for single or multi-service projects with minimal guidance. The role ensures quality deliverables are completed on time and within budget to meet customer satisfaction. The Data Team Lead provides comprehensive data management expertise to the Data Management (DM) team to deliver high-quality data management products that meet customer needs. The role includes leadership in project planning, execution, close-out activities, financial management oversight, communications, and milestone deliverables.
Qualifications:
- Bachelor’s Degree in health sciences or a related field (Required).
- 3–4 years of direct Data Management experience, including a minimum of 1 year as a CDM project lead (Preferred).
- English fluency (spoken) and advanced English proficiency.
- Advanced knowledge of computer applications such as Microsoft Excel, Word, and email tools.
- Advanced understanding of the drug development lifecycle and overall clinical research process.
Key Responsibilities:
- Gather study setup requirements through discussion and communication with relevant stakeholders.
- With minimal guidance, support, and oversight, the validation of new device integrations.
- Perform regular data cleaning activities to ensure clean data with quality and timely deliverables to sponsors.
- Ensure all deliverables meet expected quality standards and customer expectations.
- With guidance, ensure service and quality meet agreed timelines and deliverables in the contract/Scope of Work (SOW).
- Support training of new joiners.
- Lead internal study meetings, internal/sponsor audits, and participate in study kick-off meetings and sponsor meetings.
- Track and manage projects, oversee progress, identify risks, and take corrective action as required.
- With guidance, manage and oversee implementation of new technology/database revisions.
- Work closely with the programming team for process innovation and automation.
- Ensure compliance with required trainings and eSOP reading.
- Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
- Maintain collaborative communication with Line Manager and cross-functional team members.
- Perform other duties as directed by the Line Manager.
