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Clinical Data Coding information

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How much do clinical data coding jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for clinical data coding in Connecticut is $54.38, according to ZipRecruiter salary data. Most workers in this role earn between $42.98 and $64.71 per hour, depending on experience, location, and employer.

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. Coders typically work in healthcare settings and may need certification such as CPC or CCS.

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 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 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 popular job titles related to Clinical Data Coding jobs in Connecticut? For Clinical Data Coding jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Clinical Data Coding jobs in Connecticut look for? The top searched job categories for Clinical Data Coding jobs in Connecticut are:
Clinical Data Coding jobs near you
Infographic showing various Clinical Data Coding job openings in Connecticut as of July 2026, with employment types broken down into 84% Full Time, and 16% Contract. Highlights an 100% In-person job distribution, with an average salary of $113,116 per year, or $54.4 per hour.

Executive Medical Director, Neurology, Clinical Development (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Posted 18 days ago

Job description

Contact: Alexandra Spink -
No 3rd party candidates

We are looking for an accomplished Executive Medical Director, Neurology Clinical Development to lead the strategy, execution, and oversight of global clinical development programs across neurology indications. This highly visible leadership role will drive clinical programs from early development through registration, provide medical leadership across cross-functional teams, and help shape the future of our neurology gene therapy portfolio.

As the medical lead for assigned programs, you will provide expert oversight of medical monitoring, clinical strategy, data interpretation, regulatory interactions, and scientific communications. Working collaboratively across Research, Clinical Operations, Regulatory Affairs, Biostatistics, Pharmacovigilance, Commercial, and other key stakeholders, you will play a critical role in advancing innovative therapies for patients with neurologic diseases.

Key Responsibilities

  • Lead the strategy, design, and execution of global clinical development programs across Phases I–III.
  • Serve as the therapeutic area lead for the Neurology Gene Therapy Clinical Development team, partnering with Clinical Operations, Toxicology, Regulatory Affairs, Commercial, Pharmacovigilance, Clinical Quality, and Biostatistics.
  • Provide medical oversight for clinical trials, ensuring patient safety, protocol compliance, data integrity, and study quality.
  • Lead clinical operational strategy, including site selection, enrollment, feasibility, and issue resolution.
  • Collaborate with Clinical Operations on medical monitoring, safety review, coding, and data cleaning.
  • Interpret clinical trial data and ensure the scientific integrity of study reports and communications.
  • Author or oversee clinical sections of regulatory submissions, including INDs, NDAs, BLAs, and briefing books.
  • Represent the company during regulatory agency interactions and Advisory Committee meetings.
  • Develop safety management documents, DMC charters, investigator communications, and other study-related materials.
  • Build relationships with CROs, investigators, key opinion leaders, consultants, and investigational sites.
  • Analyze and present clinical data through publications, presentations, scientific meetings, and advisory boards.
  • Maintain expertise in neurology and gene therapy through scientific literature and medical conferences.
  • Manage clinical development budgets, timelines, risks, and program progress.
  • Support business development, product evaluations, due diligence, and portfolio strategy.
  • Provide medical expertise to internal and external stakeholders across research, development, commercial, regulatory, manufacturing, and patient-focused functions.
  • Coach, mentor, and develop direct reports while fostering a collaborative, high-performing team.

Qualifications

  • MD (or foreign equivalent) with clinical training and experience in Neurology required.
  • PhD in a related scientific discipline preferred.
  • 10+ years of global clinical development experience in the pharmaceutical or biotechnology industry across Phases I–III.
  • 5+ years of leadership experience managing clinical development teams.
  • Pediatric neurology experience preferred.
  • Gene therapy experience preferred.
  • Strong expertise in medical monitoring, clinical trial design, regulatory strategy, and clinical data interpretation.
  • Thorough knowledge of ICH-GCP guidelines, FDA regulations, and global clinical development requirements.
  • Excellent leadership, communication, and cross-functional collaboration skills.
  • Ability to travel domestically and internationally up to 20%.