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GSK

Develops medicines, vaccines, and consumer health

Data Lead

Clinical Research OperationsPosted on Nov 11
Full-timeBengaluru, Karnataka, IndiaNo salary listedHybrid

About the Job

Requirements

  • A bachelor's degree in a scientific or business discipline.
  • A postgraduate degree in a scientific discipline.
  • Pharmaceutical and/or contract research organization experience.
  • Understanding of the disease area.
  • Understanding of laboratory data.
  • Understanding of applicable ICH/GCP regulations and applicable GSK policies and standard operating procedures.

Responsibilities

  • Oversee end-to-end Data Strategy and Management study activities and be accountable for study deliverables, quality, and delivery to plan.
  • Manage electronic case report forms, electronic diary cards, and other clinical outcome assessments.
  • Define and execute the data management strategy, including data ingestion, cleaning, and reconciliation.
  • Deliver interim and final cleaned database locks.
  • Archive data management documents in the electronic Trial Master File.
  • Archive the study database and provide clinical data to the study site.
  • For in-house studies, lead day-to-day operational study activities, serve as a member of the study core team, and provide sponsor oversight to the Functional Service Provider working on the study.
  • For studies outsourced through Full Services Outsourcing, conduct and document sponsor oversight of end-to-end study activities.
  • Provide data management operational input into study design, protocols, study planning, study documents, and the study risk register.
  • Provide reports, status updates, feedback, and advice to key study stakeholders on study progress.
  • Create or review study-level timelines for data management deliverables and ensure teams adhere to them.
  • Promote implementation of clinical data standards to increase consistency, efficiency, and productivity.
  • Act as the first point of escalation for study data management issues; understand, mediate, resolve, and escalate issues as required to the asset-level data management representative.
  • Ensure study deliverables comply with GSK standard operating procedures and regulatory guidelines.
  • Develop and maintain professional relationships with the study team and other key stakeholders.

Desired Qualifications

  • Experience with clinical data management processes, standards, and clinical systems.
  • Project management experience.
  • Exposure to Veeva, InForm, Rave, electronic diaries, or electronic source systems.
  • Proficiency in Microsoft Excel and validation methodology.
  • Basic knowledge of PL/SQL and SAS.
  • Understanding of general data flow and database architecture concepts.
  • Good understanding of regulations including ICH-GCP, 21 CFR Part 11, and CDISC requirements.
  • Comprehensive understanding of clinical drug and vaccine development processes.
  • Knowledge of medical terminology, anatomy, and physiology.
  • CCDM certification, if present.

About the Company

GSK

Develops medicines, vaccines, and consumer health

GSK is a global healthcare company focused on three main areas: Pharmaceuticals, Vaccines, and Consumer Healthcare. It develops medicines, vaccines, and consumer health products to improve health outcomes worldwide. Its products address diseases in respiratory, HIV, oncology, and immuno-inflammatory areas; vaccines for influenza, shingles, and COVID-19; and over-the-counter wellness products. The company relies on substantial R&D and strategic partnerships to bring new products to market and to address health needs. Revenues come from sales of medicines, vaccines, and consumer health items, often complemented by patient support programs and collaborations with governments and biotech partners.

Company size
10,001+
Company stage
IPO
Headquarters
London, United Kingdom
Founded
1891

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