Lead Clinical Data Analyst

• 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 andmaintainautomation 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 beleveragedacross 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 businessobjectives.

• 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

What will you need:

Basic qualifications:

• Masters degree in a scientific or healthcare-related field.

• Minimum8-10years of experience in clinical data management or a similar role in the pharmaceutical or clinical research industry. Experience in medical devicescompanyis preferred.

• Strong understanding of clinical trial processes data managementprinciplesand regulatory guidelines.

• Proficiencyinautomation Microsoft PowerSuiteand 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 SASSQLand/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. SDTMADaM).

• Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR ICH/GCP).

• Understanding ofdata privacy and protection regulations (e.g. GDPR).

• Effective communication and interpersonal skills to collaborate with other teams.