ZipRecruiter

Log In

1

Crf Design Jobs (NOW HIRING)

EDETEK

Clinical Database Programmer

Review clinical protocol and CRF design requirements. * Support development or review of CRF specifications, edit check specifications, data validation specifications, and database build ...

Pharmaron

Senior Clinical Data Manager

Somerset, NJ · On-site

$90K - $100K/yr

This role is responsible for managing all phases of clinical data management, including study start-up, CRF design, database set-up, edit check specifications, vendor oversight, data cleaning, and ...

Jobtailor

Senior Director, Biostatistics

Cambridge, MA · On-site

$150 - $190/hr

... CRF design, DMC charter * analyzing and interpreting the clinical study results, and ensuring statistical integrity Requirements * PhD in statistics strongly preferred; Candidates with MS in ...

IQVIA

Mgr, Database Management Systems

Miami, FL · On-site

Participate in relevant study and project team meetings as standards SME and provide input for standards components, such as CRF design, CRF Completion Guidelines, programmed edit checks, Data ...

IQVIA

Mgr, Database Management Systems

Hartford, CT · On-site

Participate in relevant study and project team meetings as standards SME and provide input for standards components, such as CRF design, CRF Completion Guidelines, programmed edit checks, Data ...

next page

Showing results 1-20

All JobsCrf Design Jobs

Crf Design information

See salary details

$99.5K

$118.8K

$137.5K

How much do crf design jobs pay per year?

As of Jul 22, 2026, the average yearly pay for crf design in the United States is $118,750.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,000.00 and $127,500.00 per year, depending on experience, location, and employer.

What are CRF Designers and what do they do?

CRF Designers, or Case Report Form Designers, are professionals responsible for creating and managing the forms used to collect clinical trial data. They design electronic or paper forms that capture patient information and study data in compliance with regulatory standards. CRF Designers work closely with clinical teams to ensure data accuracy, consistency, and integrity throughout a clinical study. Their role is crucial in supporting data collection, management, and reporting for successful clinical research.

What are some common challenges faced by professionals working in CRF (Case Report Form) design, and how can they be addressed?

CRF Design professionals often encounter challenges such as ensuring data consistency across multiple study sites, balancing regulatory requirements with user-friendly layouts, and adapting forms to evolving protocol changes. Addressing these issues requires close collaboration with clinical teams, data managers, and regulatory experts throughout the design process. Utilizing electronic data capture (EDC) systems and maintaining clear documentation can also help streamline revisions and improve data quality. Continuous training and staying updated with industry standards further support effective CRF design.

What are the key skills and qualifications needed to thrive as a CRF (Case Report Form) Designer, and why are they important?

To thrive as a CRF Designer, you need a solid understanding of clinical research protocols, data management principles, and experience with CRF development, often supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems like Medidata Rave or Oracle InForm, and knowledge of regulatory standards such as CDISC, is typically required. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure accurate data collection and collaboration with cross-functional teams. These skills are crucial to produce high-quality CRFs that enable reliable data capture and regulatory compliance in clinical trials.

What is the difference between Crf Design vs Mechanical Drafting?

AspectCrf DesignMechanical Drafting
CredentialsTypically requires CAD certifications, engineering knowledgeRequires CAD skills, technical drawing certifications
Work EnvironmentDesign firms, engineering companies, manufacturingManufacturing, engineering firms, construction
Industry UsageUsed in product design, engineering projectsUsed in machinery, equipment, and structural design

Crf Design focuses on creating detailed product and engineering designs, often involving complex CAD work and engineering principles. Mechanical Drafting emphasizes technical drawings for machinery and structural components, with a stronger focus on drafting standards. While both roles require CAD skills, Crf Design involves more design development, whereas Mechanical Drafting centers on precise technical documentation.

More about Crf Design jobs
What cities are hiring for Crf Design jobs? Cities with the most Crf Design job openings:
What job categories do people searching Crf Design jobs look for? The top searched job categories for Crf Design jobs are:
Crf Design jobs near you
Infographic showing various Crf Design job openings in the United States as of July 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $118,750 per year, or $57.1 per hour.
Clinical Database Programmer

Clinical Database Programmer

EDETEK

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 16 days ago

Job description

The eClinical / Medidata Database Programmer is responsible for building, configuring, testing, and maintaining clinical study databases and related eClinical system components. This role supports clinical trial study startup, database build, edit check programming, system configuration, user acceptance testing, issue resolution, and production support.
The ideal candidate should have hands-on experience with Medidata Rave or other eClinical platforms and should understand clinical data management processes, CRF design, edit checks, visit schedules, coding setup, external data integration, and study-specific database configuration.
Essential Functions and Responsibilities
Study Database Build and Configuration
  • Build and configure study databases in Medidata Rave or other eClinical platforms based on protocol, CRF specifications, data management plan, and sponsor requirements.
  • Configure electronic case report forms, visit schedules, fields, folders, matrices, forms, dynamics, derivations, and edit checks.
  • Support setup of study-specific workflows, roles, permissions, user groups, sites, countries, and access controls.
  • Configure standard and study-specific data entry rules, validation checks, and system behavior.
  • Support setup or configuration of coding dictionaries, external data transfers, lab data, eCOA/ePRO, RTSM/IWRS, or other integrated systems as applicable.

Edit Check Programming and Validation
  • Develop and maintain edit checks, derivations, dynamics, and custom functions according to approved specifications.
  • Review edit check specifications and provide technical input to ensure checks are clear, accurate, and programmable.
  • Perform unit testing and support independent validation of database configuration and edit checks.
  • Resolve database build defects identified during testing, UAT, or production use.
  • Maintain documentation of build changes, testing evidence, and issue resolution.

CRF and Specification Support
  • Review clinical protocol and CRF design requirements.
  • Support development or review of CRF specifications, edit check specifications, data validation specifications, and database build documentation.
  • Identify inconsistencies among protocol requirements, CRFs, edit checks, and database configuration.
  • Collaborate with data managers, clinical teams, programmers, vendors, and sponsors to clarify requirements.

UAT and Production Support
  • Support user acceptance testing, including test script development, test execution, defect tracking, and resolution.
  • Assist study teams with database-related questions during study startup, conduct, and closeout.
  • Troubleshoot production database issues and implement approved changes through change control.
  • Support mid-study updates, amendments, migration activities, and post-production database changes.
  • Ensure all database changes are properly documented, tested, reviewed, and approved.

Quality and Compliance
  • Follow applicable SOPs, work instructions, validation procedures, and study-specific requirements.
  • Ensure database build activities comply with GCP, 21 CFR Part 11, audit trail expectations, and applicable regulatory requirements.
  • Maintain clear documentation for system configuration, testing, validation, and change control.
  • Support audits, inspections, and sponsor requests related to database build and eClinical system configuration.

Requirements
  • Bachelor's degree in life sciences, computer science, information systems, statistics, data management, or a related field.
  • Hands-on experience building clinical study databases in Medidata Rave, Rave EDC, or similar eClinical systems.
  • Experience with CRF design, edit check programming, database testing, and UAT support.
  • Good understanding of clinical trial processes and clinical data management activities.
  • Familiarity with GCP, 21 CFR Part 11, and computerized system validation principles.
  • Strong attention to detail and ability to follow specifications and controlled processes.
  • Good communication skills and ability to work with data management, clinical operations, programming, QA, vendors, and sponsor teams.

Preferred Qualifications
  • Medidata Rave database build experience, including Architect, Designer, Coder, Custom Functions, Amendment Manager, or related modules.
  • Experience with multiple therapeutic areas and global clinical trials.
  • Experience supporting Phase I to Phase III studies.
  • Experience with external data integration, lab data, ePRO/eCOA, RTSM/IWRS, safety systems, or central monitoring systems.
  • Experience with CDISC SDTM concepts or downstream data mapping requirements.
  • Experience supporting audits, database validation, or study migration activities.
  • Experience working in a CRO, pharmaceutical, biotech, or clinical technology environment.

Technical Skills
  • Medidata Rave or other EDC/eClinical database build tools.
  • CRF design and annotation.
  • Edit check programming and testing.
  • Custom function development, if applicable.
  • UAT test script development and execution.
  • Issue tracking and change control.
  • Basic understanding of clinical databases, data standards, and data flow.
  • Familiarity with Microsoft Excel, Word, and project tracking tools.
  • Familiarity with validation documentation and controlled system processes.

Example Deliverables
  • Study database build/configuration.
  • CRF specifications.
  • Edit check specifications.
  • Database build documentation.
  • Unit testing evidence.
  • UAT support documentation.
  • Defect and issue resolution records.
  • Change control documentation.
  • Production database update documentation.
  • Study database release package.

Benefits
Benefits vary by country, but remain competitive. Below is a sample of the benefits offered to U.S. employees.
  • Choice of comprehensive Medical, Vision and Dental Insurance plans
  • Paid vacation time and sick days
  • Corporate holidays annually
  • Participation in the 401K Plan
  • Comprehensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, etc.
  • Health Advocate and Employee Assistance Program
Location
This position may be remote, hybrid, or office-based.
Equal Opportunity Employer Statement
EDETEK is an equal opportunity employer and does not unlawfully discriminate against employees or applicants for employment on the basis of an individual's race, color, religion, creed, sex, national origin, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. Whenever possible, the company makes reasonable accommodations for qualified individuals with disabilities to the extent required by law.
Edetek logo

About Edetek

Sourced by ZipRecruiter

Industry

Software development

Company size

201 - 500 Employees

Headquarters location

Princeton, NJ, US

Year founded

2009

View All Edetek Jobs

Apply