Clinical Data Analyst: Elevate Trial Data Integrity

EDETEK Inc.; Princeton (NJ); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Medical Insurance

Vision Insurance

Dental Insurance

401(k) Plan

Paid vacation and sick days

Company holidays

Job summary

EDETEK Inc. in Princeton, NJ seeks a Clinical Data Analyst to verify trial data, ensure protocol compliance, and support regulatory submissions. The role emphasizes data accuracy, reliability, and quality across the study lifecycle.

You will oversee data management activities, design clinical and administrative reports, and collaborate with study management, biostatistics, and regulatory teams to drive efficient analyses and timely decisions.

Qualifications

• Ability to compile, code, and categorize data.
• Ability to handle multiple priorities and explore innovative solutions to problems.
• Strong interpersonal and communication skills.
• Collaborate with study management, clinical data management, biostatistics, and regulatory teams.
• Creative thinking and careful attention to detail.

Responsibilities

• Validating results and conclusions from clinical research.
• Overseeing external and internal data management activities.
• Expanding or modifying the system to serve new purposes and improve workflow.
• Designing clinical and administrative reports.
• Reviewing, extracting, compiling, and analyzing study data for compliance, quality, and accuracy, and undertaking quality improvement initiatives.
• Coordinating with other relevant departments to determine areas to be analyzed and ensure data usefulness.
• Identifying resources, developing plans for data-related projects, and determining timelines.
• Performing data validation, data reconciliation, and data surveillance.
• Conducting training for technical and software programs.

Skills

Data validation

Data management

Statistical analysis

Regulatory compliance

Communication skills

Attention to detail

Clinical trials experience

Job description

EDETEK Inc. in Princeton, NJ seeks a Clinical Data Analyst to verify trial data, ensure protocol compliance, and support regulatory submissions. The role emphasizes data accuracy, reliability, and quality across the study lifecycle.

You will oversee data management activities, design clinical and administrative reports, and collaborate with study management, biostatistics, and regulatory teams to drive efficient analyses and timely decisions.