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Lead Clinical Data Analyst
Actively Reviewing
Stryker
Job Description
What will you do:
Basic qualifications:
Preferred qualifications:
- Develop Power BI dashboards, reporting tools, and user-friendly data products that enable stakeholders to access insights independently and reduce reliance on manual reporting processes.
- Design, develop, and maintain automation solutions using Power Automate, APIs, and other technologies to streamline evidence management, reporting, data updates, and operational workflows.
- Develop integrations between platforms, applications, and data sources to enable efficient information flow, reduce duplicate effort, and improve the overall user experience.
- Develop validation processes, quality checks, and monitoring approaches that improve confidence in data used across the organization.
- Create reusable tools, workflows, and technical solutions that can be leveraged across multiple projects and business needs.
- Serve as the technical lead for Clinical Data Sciences automation, BI, and technology initiatives.
- Collaborate with stakeholders across Clinical Research, Medical Affairs, Regulatory Affairs, Market Access, and other functions as needed to support CDS-led initiatives and ensure solutions align with business objectives.
- Partner closely with the Clinical Data Sciences Manager and growing CDS team to translate strategic priorities, business needs, and evidence management challenges into scalable technical solutions
Basic qualifications:
- Master’s degree in a scientific or healthcare-related field.
- Minimum 8-10 years of experience in clinical data management or a similar role in the pharmaceutical or clinical research industry. Experience in medical devices company is preferred.
- Strong understanding of clinical trial processes, data management principles and regulatory guidelines.
- Proficiency in automation, Microsoft Power Suite and clinical data management software.
- Familiarity with relevant regulations and guidelines, like GCP and CDISC standards.
- Knowledge of industry-standard data analysis and reporting software, such as SAS, SQL and/or Oracle Clinical.
- Excellent attention to detail with problem-solving and analytical skills.
- Strong organizational and time management abilities.
Preferred qualifications:
- Certification in clinical data management (like CCDM).
- Knowledge of MS Project and analytical capabilities.
- Knowledge of CDISC standards and data interchange formats (e.g., SDTM, ADaM).
- Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).
- Understanding of data privacy and protection regulations (e.g., GDPR).
- Effective communication and interpersonal skills to collaborate with other teams.
Required Skills
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