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Crf Design Jobs (NOW HIRING)

Pharmaron

Senior Clinical Data Manager

Somerset, NJ

$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 ...

Immunome, Inc.

Senior EDC Programmer

Bothell, WA · On-site

$115K - $150K/yr

Review study protocols and provide input on CRF design and database structure. * Collaborate with Data Management to ensure alignment with data standards (CDISC, SDTM where applicable). * Perform ...

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 ...

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 ...

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 ...

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Crf Design information

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How much do crf design jobs pay per year?

As of Jun 11, 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 is a CRF design?

A CRF design refers to the creation of Case Report Forms used in clinical trials to collect and record participant data systematically. It involves designing forms that ensure data accuracy, consistency, and compliance with regulatory standards, often requiring knowledge of clinical research processes and data management tools.

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 is the highest paying clinical research job?

The highest paying clinical research jobs are typically senior roles such as Clinical Research Director or Vice President of Clinical Operations, which can offer salaries exceeding $150,000 annually. These positions require extensive experience, leadership skills, and often advanced degrees or certifications in clinical research or related fields.

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 are the 4 types of job design?

In the context of CRF Design or similar roles, the four main types of job design are task design, which involves defining specific tasks and responsibilities; work method design, focusing on how tasks are performed; work measurement, which assesses the time and efficiency of tasks; and job enrichment, aimed at increasing job satisfaction through variety and responsibility. These types help optimize productivity, safety, and employee engagement in design-related roles.

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.

What is the highest paying job in design?

In design, user experience (UX) directors and creative directors tend to have the highest salaries, often exceeding six figures annually. These roles require extensive experience, leadership skills, and proficiency with design tools like Adobe Creative Suite and Sketch, often within agency or corporate environments.
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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
Senior Clinical Data Manager

Senior Clinical Data Manager

Pharmaron

Somerset, NJ

$90K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 14 days ago

Job description

Position: Senior Clinical Data Manager

FLSA Status: Exempt

Location: Onsite (Somerset, New Jersey)

Salary: $90,000 to $100,000

About Pharmaron

Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit www.pharmaron.com.

We are seeking an experienced Senior Clinical Data Manager to lead and oversee data management activities across clinical trials while ensuring the integrity, accuracy, and reliability of clinical data. 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 database lock activities, while maintaining compliance with GCP, CDISC standards, regulatory requirements, and company SOPs.

The ideal candidate will serve as Lead Data Manager for assigned studies, coordinating resources, managing timelines and deliverables, collaborating with internal teams, sponsors, and vendors, and supporting audits and inspections. The Senior Clinical Data Manager will also contribute to process improvements, mentor team members, and provide risk management guidance to ensure high-quality project execution aligned with client expectations.

Responsibilities:

  • Ensure the integrity, reliability, and accuracy of clinical trial data.
  • Maintain clinical data quality and consistency in line with regulatory requirements, SOPs, processes, and data standards.
  • Verify external data conforms to data transfer specifications.
  • Ensure all data management activities comply with GCP, regulatory requirements, and Pharmaron Clinical/Sponsor SOPs.
  • Apply CDISC or applicable standards to data/database programming throughout the trial.
  • Adhere to Pharmaron Clinical policies and procedures.
  • Act as Lead Data Manager for clinical trials: arrange resources, assess workload, define study scope, and create timelines.
  • Oversee all data management tasks for assigned trials; monitor deliverables to meet timelines and quality standards.
  • Participate in internal/external meetings, audits, and regulatory inspections.
  • Communicate effectively with internal teams, vendors, and clients; provide risk management assessments.
  • Mentor and train team members; perform data management tasks as needed.
  • Lead project teams to deliver services aligned with client needs and contractual obligations.
  • Develop and improve clinical data management SOPs and processes; recommend improvements to senior management.

What We're Looking For:

  • Bachelor's Degree with at least 4 years' experience within a data management role, understanding of processes including study management, vendor management, CRF design, database set-up, edit check specification, DMPs, and data cleaning activities up to and including database lock.
  • Demonstrated knowledge of the functions and activities of clinical trials.
  • Demonstrated knowledge of GCP and other regulatory requirements for clinical trials.
  • CRO experience strongly preferred.

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:

  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

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