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Clinical Data Coding Jobs in New Jersey (NOW HIRING)

Clinical Data Analyst

Princeton, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information ... Ability to compile, code, and categorize data * Ability to handle multiple priorities and explore ...

Clinical Data Analyst

Princeton, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information ... Ability to compile, code, and categorize data * Ability to handle multiple priorities and explore ...

Director, Clinical Data Management

Warren, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

The Director, Clinical Data Management provides strategic and operational leadership and oversight ... Oversee and as needed, directly support coding review for adverse events, medical history and ...

... data Continually increase subject matter knowledge on our products Interact with other teams to ... code Thanks & Regards ASHOK KUMAR Sr. Lead / IT Recruiter Paradigm Infotech Call : 443-640-0099 ...

Principal Data Manager I

Bridgewater, NJ · On-site +1

$130K - $165K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... coding, medical history, adverse events, procedures and medicinal products, and external data). Assist other Clinical Research Organizations, Sponsor, or Investigative Sites with resolving queries.

Director of Coding & CDI

Egg Harbor Township, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Director Of Coding And CDI The Director of Coding and CDI will provide strategic leadership and ... This role ensures clinical data accurately reflects patient complexity, supports appropriate ...

Sr. Clinical Research Associate

Princeton, NJ · On-site +1

$90K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond ... Identify and complete follow- up of SAEs at study sites. * Assist with data listing, data coding ...

Clinical Research Associate II

Princeton, NJ · On-site +1

$80K - $110K/yr

SystImmune is seeking a high quality, ambitious and experienced Clinical Research Associate II (CRA ... Identify and complete follow- up of SAEs at study sites * Assist with data listing, data coding ...

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Showing results 1-20

Clinical Data Coding information

See New Jersey salary details

$20

$58

$83

How much do clinical data coding jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical data coding in New Jersey is $58.04, according to ZipRecruiter salary data. Most workers in this role earn between $45.87 and $69.09 per hour, depending on experience, location, and employer.

What is clinical data coding?

A Clinical Data Coding job involves assigning standardized medical codes to clinical data, such as diagnoses, procedures, and treatments, to ensure accurate documentation and facilitate healthcare analytics, billing, and research. Professionals in this role use coding systems like ICD, CPT, and SNOMED CT to classify medical information. They work with electronic health records (EHRs) and collaborate with healthcare providers, data analysts, and regulatory bodies. Accuracy and attention to detail are crucial, as coded data impacts patient care, compliance, and reimbursement.

What does a typical day look like for someone working in clinical data coding?

A typical day in Clinical Data Coding involves reviewing clinical trial data, assigning accurate codes to medical terms, adverse events, and procedures using standard classification systems, and ensuring compliance with regulatory standards. You’ll collaborate closely with clinical data managers, medical reviewers, and biostatisticians to resolve discrepancies and maintain data integrity. Additionally, you may attend team meetings to discuss coding conventions or project updates and perform quality checks on coded data. This role offers a structured environment where attention to detail and accuracy are highly valued, supporting the success of clinical research projects.

What are the key skills and qualifications needed to thrive in clinical data coding, and why are they important?

To thrive in Clinical Data Coding, strong knowledge of medical terminology, clinical research processes, and disease classification systems (such as ICD-10 or MedDRA) is generally required, often supported by a degree in life sciences or related fields. Familiarity with electronic data capture systems, clinical trial databases, and specialized coding software is essential, along with certifications like Certified Clinical Data Manager (CCDM) or Certified Clinical Research Professional (CCRP) being advantageous. Attention to detail, analytical thinking, and effective communication enhance quality and teamwork in this role. These skills and qualities ensure precise and compliant data coding, which is critical for research integrity, regulatory submissions, and high-quality clinical outcomes.

What does a clinical data coder do?

A clinical data coder reviews medical records and assigns standardized codes to diagnoses, procedures, and treatments using coding systems like ICD and CPT. This process ensures accurate billing, data analysis, and compliance with healthcare regulations, often requiring attention to detail and familiarity with coding software. Certification such as CPC is commonly preferred in this role.
Infographic showing various Clinical Data Coding job openings in New Jersey as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $120,720 per year, or $58 per hour.

Clinical Data Analyst

EDETEK

Princeton, NJ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 16 days ago


Job description

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information professional responsible for verifying the validity of clinical trials and data gathered. He/she will ensure that processes and protocols are followed, regulations and company standards are followed, and the analysis goals are achieved, with quality and efficiency.

A Clinical Data Analyst’s primary responsibility is to ensure that data is accurate and reliable throughout the clinical trial conduct, analysis, and regulatory submission. The information collected and produced is free of errors, relevant, and sound. All in all, a Clinical Data Analyst is at the center of data management for an organization, right from planning and execution to completion of a clinical study phase.

Essential Functions and 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 (e.g., study management team, clinical operations, clinical data management, and biostatistics) to determine the areas to be analyzed and see that appropriate measures are taken to ensure data analysis is useful
  • identifying necessary resources, developing plans for data-related projects, and determining timelines and milestones
  • performing data validation, data reconciliation, and data surveillance
  • conducting training for technical and software programs

Requirements

Education and Experience Required

  • Ability to compile, code, and categorize data
  • Ability to handle multiple priorities and explore innovative solutions to problems
  • Strong interpersonal and communication skills
  • Tackling complex situations involving study management and conduct teams, clinical data management, biostatisticians, and regulatory agencies.
  • Creative thinking, an eye for detail, working independently.

Ability to compile, code, and categorize data

  • Ability to handle multiple priorities and explore innovative solutions to problems
  • Strong interpersonal and communication skills
  • Tackling complex situations involving study management and conduct teams, clinical data management, biostatisticians, and regulatory agencies.
  • Creative thinking, an eye for detail, working independently

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

Princeton, NJ preferred; applicants based in Brazil and Argentina are also encouraged to apply.

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.


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About Edetek

Sourced by ZipRecruiter

Industry

Software development

Company size

201 - 500 Employees

Headquarters location

Princeton, NJ, US

Year founded

2009