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Clinical Documentation Improvement Manager Jobs in Decatur, GA

Hospital Inpatient Coder III

Decatur, GA · On-site

$21.25 - $25.75/hr

Works closely with physicians, clinical documentation improvement specialist, quality, and patient finance staff. Plays a key role in billing, research, internal and external reporting, and ...

Hospital Inpatient Coder III

Lithonia, GA · On-site

$19.75 - $24/hr

Works closely with physicians, clinical documentation improvement specialist, quality, and patient finance staff. Plays a key role in billing, research, internal and external reporting, and ...

Coach clinical and administrative staff on quality improvement methodologies and support ongoing ... Ability to manage multiple projects independently and in coordination with cross-functional teams ...

Participate in quality improvement initiatives and clinical audits. Required Qualifications ... management * Infection prevention and control * Electronic Medical Records (EMR/EHR) documentation

Auditor, Risk Adjustment

Atlanta, GA · Remote

$82K - $108K/yr

Quality audits are specific to ICD-10 code abstraction relative to accuracy, completeness, and identified clinical documentation improvement opportunities. You will work with management to implement ...

Support AI-assisted documentation evaluation and quality improvement initiatives. Required Skills * Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific ...

Showing results 21-40

Clinical Documentation Improvement Manager information

See Decatur, GA salary details

$38.6K

$105.8K

$159.1K

How much do clinical documentation improvement manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for clinical documentation improvement manager in Decatur, GA is $105,848.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,500.00 and $143,000.00 per year, depending on experience, location, and employer.

What is a clinical documentation improvement manager?

A Clinical Documentation Improvement (CDI) Manager is a healthcare professional responsible for overseeing programs that ensure clinical documentation accurately reflects patients’ diagnoses, treatments, and care provided. They work closely with physicians, nurses, and coding staff to clarify medical record information, improve documentation quality, and support accurate coding and billing. This role helps enhance patient care, ensure compliance with regulations, and optimize hospital reimbursement. CDI Managers often lead a team of specialists, provide training, and implement best practices in clinical documentation.

How does a clinical documentation improvement manager collaborate with physicians and clinical staff to enhance documentation quality?

A Clinical Documentation Improvement Manager regularly works alongside physicians, nurses, and coding teams to ensure clinical documentation accurately reflects patient care and supports appropriate coding and reimbursement. This often involves conducting educational sessions, providing real-time feedback, and facilitating query processes when additional clarification is needed. Effective communication and relationship-building are essential, as the manager must bridge the gap between clinical language and coding requirements while promoting best practices across departments. Collaboration is often ongoing, with frequent meetings and interdisciplinary rounds to review complex cases and address documentation challenges.

What are the key skills and qualifications needed to thrive as a clinical documentation improvement manager?

To thrive as a Clinical Documentation Improvement Manager, you need an in-depth understanding of clinical terminology, coding standards (ICD-10, CPT), and healthcare regulations, usually backed by a degree in nursing, HIM, or a related field. Familiarity with electronic health record (EHR) systems, clinical documentation improvement (CDI) software, and relevant certifications such as CCDS or CDIP is essential. Strong analytical thinking, attention to detail, and excellent communication skills are crucial for collaborating with clinicians and educating staff. These skills ensure accurate, complete documentation, which supports optimal patient care, regulatory compliance, and proper revenue cycle management.

What is the difference between Clinical Documentation Improvement Manager vs Clinical Documentation Specialist?

AspectClinical Documentation Improvement ManagerClinical Documentation Specialist
CredentialsTypically requires RHIT, RHIA, or CCS certificationsOften holds CCS, CPC, or RHIT certifications
Work EnvironmentOversees teams in hospitals or health systems, focusing on documentation qualityWorks directly with physicians and coding staff to improve documentation
Industry UsageUsed in healthcare organizations to lead CDI programsCommonly employed in hospitals to enhance clinical records
Search & Comparison IntentOften compared for leadership roles in CDICompared for direct documentation improvement tasks

The Clinical Documentation Improvement Manager oversees CDI teams and strategies, focusing on program leadership, while the Clinical Documentation Specialist works directly on improving clinical records through collaboration with healthcare providers. Both roles require similar certifications and are integral to healthcare documentation quality, but differ mainly in scope and responsibilities.

What are popular job titles related to Clinical Documentation Improvement Manager jobs in Decatur, GA?

For Clinical Documentation Improvement Manager jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Clinical Documentation Improvement Manager jobs in Decatur, GA look for?

The top searched job categories for Clinical Documentation Improvement Manager jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Clinical Documentation Improvement Manager jobs?

Cities near Decatur, GA with the most Clinical Documentation Improvement Manager job openings:

Infographic showing various Clinical Documentation Improvement Manager job openings in Decatur, GA as of August 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $105,848 per year, or $50.9 per hour.

Medical Writer / Clinical Document Author

micro1 AI

South Fulton, GA • Remote

$50 - $80/hr

Part-time

Posted 17 days ago


Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.