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Crf Design Jobs (NOW HIRING)

Integrated Resources INC

SAS Programming

Madison, NJ · On-site

Reviews case report form (CRF) design; Designs and/or reviews database structure; Writes edit checks from the Data Cleaning Plan (DCP) specifications; Creates derived-analysis datasets; Executes ...

Icon plc

Senior Biostatistician

Blue Bell, PA

Responsible for statistical aspects of CRF design and edit specifications. * Performs statistical analyses and interprets results for simple to complex clinical studies. * Reviews simple to complex ...

ICON

Senior Biostatistician

Blue Bell, PA · On-site +1

Responsible for statistical aspects of CRF design and edit specifications. * Performs statistical analyses and interprets results for simple to complex clinical studies. * Reviews simple to complex ...

Medpace, Inc.

Biostatistician I

Cincinnati, OH · On-site

Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and * Communicate statistical results to medical ...

Everest Clinical Research

Senior Biostatistician

$130K/yr

Provide statistical input to Case Report Forms (CRF) design and database/variable structure. * Provide statistical input to non-CRF data collection and acquisition methods and approaches. * Review ...

Medpace, Inc.

Biostatistician I

Cincinnati, OH

Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and * Communicate statistical results to medical ...

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Crf Design information

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$99.5K

$118.8K

$137.5K

How much do crf design jobs pay per year?

As of Jul 1, 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
Vice President, Biometrics

Vice President, Biometrics

Janux Therapeutics

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago

Job description

Reporting to the Chief Medical Officer, the Vice President, Biometrics will lead and oversee all biometrics activities supporting clinical development from IND-enabling studies through regulatory submission. This role is responsible for Biostatistics, Statistical Programming, and Clinical Data Management, and will serve as the functional head of Biometrics at Janux.

The VP will work closely with senior leadership to shape clinical strategy, study design, regulatory planning, and data-driven decision-making. This role requires a highly strategic and collaborative leader who can also operate hands-on in a dynamic, fast-paced clinical-stage biotech environment.

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
  • Provide strategic and operational leadership for the Biometrics function, including Biostatistics, Statistical Programming, and Clinical Data Management.
  • Build, lead, and develop a high-performing biometrics organization, including internal staff, consultants, and external partners (e.g., CROs and vendors).
  • Lead biometrics strategy and execution across clinical development programs from early development through submission readiness and post-submission support.
  • Serve as the biometrics functional lead on cross-functional development teams, contributing to study design, statistical strategy, endpoint selection, and key development decisions.
  • Act as a trusted advisor to senior leadership on statistical methodologies, data strategy, data integrity, and clinical development planning.
  • Oversee the design, analysis, and interpretation of clinical trials and preclinical studies, ensuring scientific rigor, regulatory compliance, and high-quality data standards.
  • Provide oversight and strategic guidance for statistical analysis plans (SAPs), Tables, Listings, and Figures (TLFs), clinical study reports (CSRs), integrated summaries, and regulatory submission deliverables.
  • Ensure all biometrics deliverables meet applicable regulatory standards and industry best practices, including CDISC, SDTM, ADaM, and related requirements.
  • Support and lead preparation for regulatory interactions and inspections; represent Biometrics in meetings with FDA, EMA, and other global health authorities as appropriate.
  • Collaborate closely with Clinical Development, Clinical Operations, Regulatory Affairs, Translational Sciences, Pharmacovigilance, and Quality teams to ensure alignment on study design, execution, and data quality.
  • Provide oversight of CRO and vendor deliverables, including database build, CRF design, data review, programming outputs, and TLF production, ensuring quality, timelines, and cost-effectiveness.
  • Establish and maintain biometrics systems, standards, processes, and SOPs, including frameworks for CRF development, data collection, database management, and data governance.
  • Drive innovation in statistical methodology, adaptive trial design, data analytics, visualization, and technology-enabled processes to support program advancement and decision-making.
  • Ensure appropriate resourcing across the biometrics organization, including workforce planning, budget management, and vendor strategy.
  • Support business development, diligence, and strategic partnership activities as the biometrics subject matter expert.
  • Represent the company externally in scientific, regulatory, and industry forums, as appropriate.
EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS, AND ABILITIES
  • PhD in Biostatistics, Statistics, or a related quantitative discipline required.
  • 15+ years of experience in biotechnology or pharmaceutical drug development, including significant leadership experience in biometrics.
  • Proven experience leading integrated biometrics functions across Biostatistics, Statistical Programming, and Clinical Data Management.
  • Deep experience across all phases of drug development, ideally spanning early-stage development through registration and commercialization support.
  • Strong background in oncology therapeutics and drug development; experience in immunology, autoimmune disease, or related therapeutic areas is highly desirable.
  • Demonstrated success supporting regulatory submissions and health authority interactions, including NDA/BLA filings and advisory committee preparation.
  • Extensive knowledge of clinical trial design, statistical methodology, adaptive designs, and applicable regulatory requirements and guidance (ICH, FDA, EMA, GCP).
  • Strong technical expertise, including familiarity with SAS, R, CDISC standards, electronic data capture systems, and modern clinical data platforms.
  • Proven ability to build, mentor, and scale high-performing teams in a collaborative and accountable culture.
  • Strong executive presence with excellent communication, presentation, and influencing skills
  • Demonstrated ability to operate effectively in a fast-paced, hands-on, clinical-stage biotech environment with evolving priorities.
  • Strong organizational skills with the ability to manage multiple programs and deadlines simultaneously.
  • Commitment to scientific excellence, operational rigor, and continuous process improvement.
  • Ability to travel up to 25% as business needs require.
$330,000 - $360,000 a year

In addition to a competitive base salary ranging from $330,000 to $360,000, we offer stock options, restricted stock units, a stock purchase plan (ESPP) and a target bonus.  Janux also provides a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance. Relocation assistance may also be available.

Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, internal equity, and work location.

Benefits:

  • Annual bonus program
  • Incentive stock option plan
  • 401k plan with flat non-elective employer contribution
  • Comprehensive medical insurance with 90-100% employer-paid premiums
  • Dental and vision insurance
  • HSA, FSA, and supplemental insurance plans (life, disability, accident, critical illness, hospital indemnity)
  • Unlimited PTO
  • Generous holiday schedule; includes summer and winter company shutdown
  • Relocation assistance

Schedule:

  • Monday to Friday

 

Work authorization:

  • United States (Required)

 

Additional Compensation:

  • Annual targeted bonus %

 

Work Location:

  • Hybrid preferred in San Diego office. Remote permitted upon approval, with ability to travel up to 25% for meetings or site visits as required.

 

Travel:

  • Up to 25% travel may be required, including domestic and occasional international travel for regulatory meetings, CRO oversight, investigator meetings, scientific conferences, and corporate activities.

 

EQUAL OPPORTUNITY EMPLOYER:

Janux Therapeutics, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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