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Senior Clinical Data Management Professional
Novo NordiskSenior Clinical Data Manager managing complex clinical data activities for trials at Novo Nordisk. Focus on data quality, stakeholder collaboration, and regulatory compliance.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Data Management, ensuring data quality and integrity throughout the clinical trial lifecycle. Proficient in project coordination, stakeholder management, and compliance with regulatory requirements such as ICH-GCP.
Highest-signal resume keywords
Clinical Data ManagementProject CoordinationStakeholder ManagementRegulatory ComplianceData Quality Assurance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ProcessesData Collection StrategiesData Integrity ManagementRisk ManagementQuality Plans Development
Soft Skills
CollaborationCommunicationProblem-Solving
Industry Keywords
Pharmaceutical IndustryBiotechnologyCRO IndustryICH-GCPData Management Activities
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Planning, coordinating, and delivering data management activities across one or more clinical trials.
- Ensuring data quality, integrity, and timely delivery of clinical trial data throughout the study lifecycle.
- Acting as the Data Management lead for assigned trials.
- Collaborating with colleagues, vendors, and global stakeholders.
- Defining and overseeing data collection strategies, standards, and quality plans.
- Managing risks, issues, and dependencies related to trial data.
- Contributing to continuous improvement initiatives and the implementation of innovative ways of working.
- Supporting inspection and audit readiness activities.
Requirements
What you’ll need- A degree (BSc, MSc, or equivalent) in Life Sciences, Health Sciences, Data Science, Information Technology, or a related field.
- More than three years of experience within Clinical Data Management in the pharmaceutical, biotechnology, or CRO industry.
- Solid understanding of clinical trial processes, clinical data flow, and regulatory requirements including ICH-GCP.
- Experience leading Data Management activities for complex clinical trials.
- Strong project coordination and stakeholder management skills.
- Experience working in cross-functional and international environments.
- Fluency in written and spoken English.
Benefits
Comp & perks- continuous learning
- career development
- benefits tailored to your life and career stage