Back
Tier-1 employer, metro location, mid-level lead title, and generalist DM skillset increase applicant competition.
Clinical data management requires industry-specific regulatory and trial experience, limiting cross-industry transferability.
Regulated clinical DM, mandatory SOP/regulatory experience and domain expertise enforce strict screening.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Own end-to-end Data Science & Management (DS&M) study activities including data ingestion, cleaning, reconciliation, database lock, and archival of DM documents and study database.
Lead day-to-day DS&M operations for in-house studies or oversee vendor Functional Service Providers' DS&M activities ensuring compliance, training, and quality delivery.
Provide operational input into study design and planning, monitor timelines, report progress to stakeholders, and act as escalation point for DS&M issues ensuring GSK SOP and regulatory compliance.
Experience in managing end-to-end clinical data management processes including case report forms, vendor data, and clinical outcome assessments.
Demonstrated oversight and coordination of DS&M activities either in-house or via outsourced Functional Service Providers.
Knowledge of regulatory guidelines and GSK SOPs related to clinical data management.
Work Experience Required: Not explicitly mentioned in the JD.
Experienced in clinical data management within pharmaceutical or biopharma environments with accountability for study delivery and vendor oversight.
Strong operational leader capable of managing multi-stakeholder study teams and ensuring adherence to timelines and quality standards.
Able to provide strategic input into study design and risk management, with advanced understanding of data standards and clinical trial processes.