Back
Tier-1 brand plus mid-level managerial role and on-premise requirement create moderate applicant competition.
Clinical trial data management is highly industry-specific, limiting transferability across unrelated industries.
Regulatory/GCP adherence, SOP compliance and managerial accountability impose stringent domain-specific hiring filters.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Own end-to-end Clinical Data and Information Sciences (CDIS) deliverables and data quality for one or more clinical trials.
Lead and provide oversight to Data Managers and internal/external stakeholders to ensure inspection readiness and adherence to data standards.
Drive operational excellence and quality risk management by collaborating with cross-functional Core Study Team and applying CDIS best practices.
Work Experience Required: Not explicitly mentioned in the JD
Mandatory adherence to applicable SOPs, regulations, GCDMPs, and ALCOA principles in clinical data management.
Experience coordinating CDIS deliverables including Data Management Plan and quality risk indicators in clinical trials.
On-premise work location requirement.
Experienced in managing clinical trial data delivery and quality across multiple studies in a regulated environment.
Proven leadership capability to direct Data Managers and collaborate broadly with cross-functional teams in clinical development.
Strong operational focus with ability to execute CDIS strategies ensuring study milestones and inspection readiness.