Senior Clinical Database Designer

Everest Clinical Research

Senior Clinical Database Designer at Everest Clinical Research enhancing clinical database design. Collaborating with teams and contributing to the development of efficient data management processes across projects.

Posted 5/27/2026full-timeRemote • New Jersey • 🇺🇸 United StatesSenior💰 $90,000 - $130,000 per yearWebsite

About the role

Key responsibilities & impact

Develop new features and functionality within the database design functional areas
Assist Clinical Data Management in planning, directing, and managing the clinical database design and maintenance process
Review the protocol and associated study reference materials
Maintain database design timelines
Follow up on regulatory requirements, industry trends, benchmarking, and best working practices
Design and review case report forms (CRFs/eCRFs)
Author and review the Data Validation Specifications
Develop and review User Acceptance Test (UAT) plans
Coordinate and oversee the UAT process
Design and review patient Case Report Forms and database schema
Test data capture/entry screens through UAT
Participate in EDC vendor’s technical learning and exchange meetings
Provide user training to CRAs on EDC systems
Contribute to the development and maintenance of the company’s database design procedural documents
Plan, manage, control and perform data processing activities for assigned projects
Review the Data Management Plan (DMP)
Review data, issue and resolve queries
Assist in resolving medical coding discrepancies
Cooperate with the Quality Assurance Department with quality control audits
Define and monitor clinical trial data flow and quality control processes
Accurately and efficiently validate electronically captured data
Write clear queries on missing data and data points failing pre-defined range checks
Develop and test SAS codes for clinical trial database logical checks and study specific monitoring reports.

Requirements

What you’ll need

B.Sc. in Biological Sciences or Computer Science
Five years' related experience
Two to three years developing Inform and/or Medidata Rave (or similar) clinical data bases
Previous Clinical Data Management experience in both paper based and electronic data capture systems
Must communicate effectively, orally and in writing, with personnel on all professional and administrative levels
Proven leadership and interpersonal skills in complex team situations
Excellent presentation skills and ability to build relationships with both internal and external clients
Must be well organized and able to work independently and manage multiple projects/tasks appropriately
Demonstrated ability to effectively organize and integrate the activities of information processing personnel.

Benefits

Comp & perks

medical, dental, and vision coverage
life & AD&D insurance
short- and long-term disability
tuition reimbursement
fitness reimbursement
employee assistance program (EAP)
a 401(k) retirement
generous paid time off
sick leave
opportunity to earn a performance based bonus

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

database designclinical database designData Validation SpecificationsUser Acceptance Testing (UAT)data processingSAS codingdata capturedata validationmedical codingclinical trial monitoring

Soft Skills

effective communicationleadershipinterpersonal skillspresentation skillsrelationship buildingorganizational skillsindependent workproject managementteam collaborationproblem-solving

Certifications

B.Sc. in Biological SciencesB.Sc. in Computer Science