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clinical documentation specialist

Emory Healthcare

<div>
 
 Overview
 
 
 
 
 Be inspired. Be rewarded. Belong. At Emory Healthcare.
 
 
 
 
 Benefits
 
 
 
 At Emory Healthcare we fuel your professional journey with better benefits, valuable resources, ongoing mentorship and leadership programs for all types of jobs, and a supportive environment that enables you to reach new heights in your career and be what you want to be. We provide:
 
 
 <ul>
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 Comprehensive health benefits that start day one!
 </li>
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 Student Loan Repayment Assistance &amp; Reimbursement Programs
 </li>
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 Family-focused benefits
 </li>
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 Wellness incentives
 </li>
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 Ongoing mentorship, development, leadership programs&hellip;. and more!
 
 
 </li>
 </ul>
 
 Description
 
 
 
 We're seeking a
 
 Clinical Documentation Specialist (Registered Nurse / RN)
 
 who provides clinically based concurrent and retrospective review of inpatient medical records to evaluate the documentation of patient acuity and to support acute care services that were delivered. The goal of concurrent review includes facilitation of appropriate physician documentation of care delivery to accurately reflect patient severity of illness and risk of mortality. Specific reviews are both determined internally and by requirements/requests of external payers or regulatory agencies and play a significant role in reporting quality of care outcomes and in obtaining accurate and compliant documentation for billing of services rendered.
 
 
 
 Minimum Qualifications
 
 
 
 <ul>
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 Graduate of an accredited school of Nursing, or United States or International School of Medicine Education.
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 For RNs, candidates must have an active license.
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 All nurses employed in roles requiring an unencumbered nursing license must have a valid, active license or temporary permit approved by the Georgia Licensing Board.
 </li>
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 Education and experience may be considered in lieu of a RN license for highly qualified candidates (physician).
 </li>
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 Three years' experience in healthcare related field with strong clinical expertise and acumen.
 </li>
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 Prefer recent clinical experience in an acute care setting, (Critical Care, Medical/Surgical or Emergency department nursing preferred; or 2 years' experience in a specialty area).
 
 
 </li>
 </ul>
 
 JOIN OUR TEAM TODAY!
 
 Emory Healthcare (EHC), part of Emory University (EUV), is the most comprehensive academic health system in Georgia and the first and only in Georgia with a Magnet&reg; designated ambulatory practice. We are made up of 11 hospitals-4 Magnet&reg; designated, the Emory Clinic, and more than 425 provider locations. The Emory Healthcare Network, established in 2011, is the largest clinically integrated network in Georgia, with more than 3,450 physicians concentrating in 70 different subspecialties.
 
 
 
 Additional Details
 
 
 
 Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law.
 
 
 Emory Healthcare is committed to providing reasonable accommodations to qualified individuals with disabilities upon request. Please contact Emory Healthcare&rsquo;s Human Resources at careers@emoryhealthcare.org . Please note that one week's advance notice is preferred.
</div>

Clinical Documentation Specialist

SynerGrx

About SynerGrx:SynerGrx is a patient-centered clinical pharmacy service provider focused on integrating pharmacists into care teams to improve outcomes and enhance chronic care management. We deliver innovative ambulatory care services while empowering pharmacists to practice at the top of their license in collaborative clinical environments.Position Summary:We are seeking an experienced and driven Clinical Pharmacist &ndash; Ambulatory Care to join our growing team. This role plays a key part in executing clinical service programs and supporting direct patient care initiatives. The Clinical Pharmacist (CP) will work under the direction of the Director of Clinical Services (DCS) and serve as a leader and implementation specialist within the clinical team.Key Responsibilities:Clinical Services &amp; Patient Care<ul><li>Review and verify prescriptions from authorized prescribers</li><li>Provide comprehensive medication counseling, addressing side effects, interactions, dosage, and storage</li><li>Perform Drug Utilization Reviews (DUR)</li><li>Deliver direct patient care including Chronic Care Management (CCM), Remote Patient Monitoring (RPM), and Continuous Glucose Monitoring (CGM)</li><li>Provide Medication Therapy Management (MTM) services</li><li>Integrate into medical practice workflows and collaborate closely with providers</li></ul>Collaborative Practice<ul><li>Follow established collaborative practice agreements and protocols</li><li>Maintain professional relationships with internal and external stakeholders</li><li>Provide timely feedback to the DCS on clinical outcomes and provider engagement</li></ul>Leadership &amp; Administration<ul><li>Manage and supervise staff pharmacists and clinical pharmacy technicians</li><li>Oversee KPI performance and assist in quality improvement initiatives</li><li>Provide coverage planning for team schedules and time-off requests</li><li>Contribute to the development and execution of clinical programs and business objectives</li></ul>Qualifications:<ul><li>Doctor of Pharmacy (PharmD) degree</li><li>Active Georgia pharmacist license</li><li>Post-graduate residency (PGY1) preferred or 2+ years of direct patient care experience in ambulatory care or similar setting</li><li>Immunization and MTM Certifications</li><li>BLS-CPR certified</li><li>Minimum 30 CPE hours every 2 years (20+ hours focused on chronic disease management)</li></ul>Skills &amp; Competencies:<ul><li>Strong clinical judgment and decision-making skills</li><li>Excellent interpersonal, communication, and leadership abilities</li><li>Team player with a commitment to collaboration and respect</li><li>Business acumen and understanding of regulatory compliance</li><li>Able to work independently and adapt to changing priorities</li></ul>Physical Requirements:<ul><li>Ability to stand for long periods</li><li>Lift and carry up to 25 pounds (occasionally up to 50 pounds)</li><li>Manual dexterity for routine pharmacy operations</li><li>Normal vision, speech, and hearing (corrected if necessary)</li></ul>Benefits:<ul><li>Competitive salary</li><li>401(k) with 5% company match when employee contributes 4%</li><li>Medical, dental, and vision insurance</li><li>Paid time off and holidays</li><li>Life insurance</li><li>Short and long-term disability coverage</li><li>Financial wellness resources</li></ul>Why Join SynerGrx?Be part of a forward-thinking pharmacy team committed to transforming ambulatory care. We offer a supportive work environment, opportunities for leadership, and the ability to make a meaningful difference in patient lives every day.Job Type: Full-timePay: $120,640.00 - $128,960.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Flexible schedule</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Ability to Commute:<ul><li>Atlanta, GA 30341 (Required)</li></ul>Ability to Relocate:<ul><li>Atlanta, GA 30341: Relocate before starting work (Required)</li></ul>Work Location: Hybrid remote in Atlanta, GA 30341

Clinical Pharmacist - Ambulatory Care

Atlanta Diabetes Associates

<div>Description:

SUMMARY
This position will support the administrative and clinical functions of a clinical research department. 
Responsibilities include data entry, supply room management, patient recruitment, department marketing, equipment monitoring, and laboratory processing.
DUTIES
Performs a combination, but not necessarily all, of the following duties: 
Assists Clinical Research Coordinator in the conduct of clinical trials. 
Accepts shipments of study supplies and maintains organization of study supply room. 
Monitors department equipment and maintains documentation logs 
Performs phlebotomy and processes, packages, and ships labs. 
Performs data entry of clinical trial information as needed. 
Assists in the organization and storage of source documentation. 
Assists in patient recruitment with direct patient contact and by keeping providers informed of enrolling trials. 
Assists in developing marketing materials for research department and in developing website content. 
Performs other duties as assigned.
SUPERVISION
Work is performed under general supervision from the Principal Investigator and Department Manager of the research unit. (Investigator acts as consultant on any problems which arise).
ADDITIONAL RESPONSIBILITIES<ul><li>
Handle and protect confidential and sensitive data with integrity.</li><li>
Manage data collection projects by meeting paper and electronic mailing deadlines, entering data, transcribing tapes and handwritten notes; learn and use technology to do these tasks more efficiently.</li><li>
Prepare print documents, web pages, and other graphics using Word and Excel.</li><li>
Produce written, tabular and visual materials for research reports and presentations.</li></ul>
EDUCATION/EXPERIENCE
Associate degree preferred. Experience may be accepted in lieu of formal education. 
Experience working in medical office, laboratory, or research center preferred.
EQUIPMENT
Must be familiar with scientific and medical equipment used in the particular field of laboratory, medical and clinical research.
WORKING CONDITIONS
Work is performed in an office, laboratory, and/or clinic environment. This is a full-time position. 
Full-time is defined as 40 hours per work week. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Management retains the right to add or to change the duties of the position at any time.
IMPORTANT:
Any qualifications to be considered as equivalents in lieu of stated minimums require prior approval of the Division Manager, Principal Investigator and Chief Operations Officer. 
Information resources including data, information, technology, and software are Atlanta Diabetes Associates resources and must be protected and used in conformance with all applicable laws and policies in accordance with Information Security Standards.
Requirements:

 SKILLS AND QUALIFICATIONS
Required abilities and dispositions:<ul><li>
High personal motivation, self-management, and detail-orientation; ability to take responsibility in meeting deadlines and making progress without direct supervision.</li><li>
Strong spoken and written communications skills.</li><li>
Capacity and will to learn new software, research methods, and work routines quickly; flexibility in responding to new research opportunities as they arise.</li><li>
Motivation to engage in and manage a wide range of intellectual and physical work, ranging from preparing mass mailings to analyzing proposed data-collection designs.</li><li>
Strong existing computer skills with Microsoft Office statistical software, and general Internet and electronic communications.</li><li>
Articulate and tactful communications skills; readiness to meet and work directly with clients.</li></ul>
Job Type: Full-time
Pay: From $22.00 per hour
Benefits:<ul><li>
401(k)</li><li>
401(k) matching</li><li>
Dental insurance</li><li>
Health insurance</li><li>
Life insurance</li><li>
Paid time off</li><li>
Vision insurance</li></ul>
Schedule:<ul><li>
Monday to Friday</li></ul>
Ability to commute/relocate:<ul><li>
Atlanta, GA 30318: Reliably commute or planning to relocate before starting work (Required)</li></ul>
Experience:<ul><li>
Clinical trials: 1 year (Preferred)</li><li>
Research: 1 year (Preferred)</li></ul>
Work Location: In person</div>

RESEARCH ASSISTANT I

Brooksource

<div>
 
 
 Job Title:
 
 Jr Data Entry Specialist
 
 
 
 Location:
 
 Atlanta, GA (ATL preferred)
 
 
 
 Schedule:
 
 Onsite, 5 days/week
 
 
 
 Perks:
 
 Free parking
 
 
 
 About the Role
 
 
 
 We&rsquo;re seeking a Jr Data Entry Specialist to support property and vendor setup while ensuring accurate and timely commission processing. This role is ideal for someone highly detail-oriented who can follow established processes, work across multiple databases, and handle sensitive financial information with care. It&rsquo;s a strong opportunity for someone eager to gain exposure to a corporate operations environment.
 
 
 
 What You&rsquo;ll Do
 
 
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 Enter and maintain new properties in internal systems (supporting 170&ndash;190+ properties)
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 Set up new vendors and establish vendor IDs in coordination with Accounts Payable
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 Review and verify tax documentation to ensure vendors are eligible for compensation in their respective states
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 Confirm contract payment terms and validate unit counts eligible for compensation
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 Calculate and process commissions using internal systems and Excel-based uploads
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 Research unpaid commissions and resolve discrepancies or incorrect payments
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 Initiate recoupment for overpayments or invalid payments
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 Receive and route returned checks to Accounts Payable
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 Work through and resolve an existing ticket backlog (approximately 700 tickets from 2025 to present)
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 Pull and reconcile data from multiple internal databases while maintaining accuracy
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 Handle private banking and compensation data securely within VPN environments
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 </ul>
 
 
 What We&rsquo;re Looking For
 
 
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 High attention to detail and ability to follow defined processes consistently
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 Comfort working across multiple systems and accurately transferring information
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 Strong Excel skills; experience uploading or reconciling spreadsheet-based data
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 Proficiency in Microsoft Outlook and professional internal communication
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 Ability to work independently and stay organized in a high-volume environment
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 Strong interest in gaining exposure to a corporate operations role
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 </ul>
 
 
 Nice to Have
 
 
 <ul>
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 Experience working with large datasets or running SQL queries (not required)
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 Background in data entry, operations, finance, or administrative roles
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 </ul>
 
 
 Why This Role
 
 
 <ul>
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 Onsite exposure to a structured corporate environment
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 Clear processes, hands-on work, and defined expectations
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 Growth opportunity for early-career candidates or those transitioning from service or hospitality roles
 </li>
 </ul>
 
 
</div>

Data Entry Specialist

Progressive Counseling

Progressive Consumer Counseling Services is seeking a Board-Eligible or Board-Certified Psychiatrist to provide psychiatric evaluation and medication management for adult and child/adolescent clients in an outpatient setting. This is a hybrid position, with most services delivered via HIPAA-compliant telehealth and scheduled in-office coverage twice per month.Responsibilities<ul><li>Conduct psychiatric evaluations and ongoing medication management for adult and child/adolescent clients</li><li>Diagnose mental health conditions using DSM-5-TR criteria</li><li>Prescribe and monitor psychotropic medications</li><li>Complete Mental Status Exams (MSE) and AIMS assessments as clinically indicated</li><li>Collaborate with therapists, nurse practitioners, and clinical leadership on treatment planning</li><li>Develop and support person-centered treatment plans</li><li>Provide education to clients and families regarding diagnoses, medications, and side effects</li><li>Participate in scheduled on-site clinical days and virtual team meetings</li><li>Coordinate care with primary care providers, inpatient facilities, and other community partners</li><li>Respond to clinical concerns and support crisis planning as needed</li><li>Maintain timely, accurate documentation in the electronic health record</li><li>Ensure compliance with HIPAA, CARF, DBHDD, and professional standards</li></ul>Job Type: Part-timePay: $200.00 - $225.00 per hourWork Location: Hybrid remote in Atlanta, GA 30349

Psychiatrist

EYE CONSULTANTS OF ATLANTA

<div>Job Description<div><div> 
Job: 
Ophthalmic Scribe 
EEOC: 
Technician</div><div> 
Status: 
Non-Exempt 
Department: 
Clinical</div></div> 
Position Overview: The role of the scribe is to assist the physician with documentation of the patient's medical record. This role ensures a seamless patient experience by facilitating effective communication and allowing the physician to focus on patient care.
Responsibilities:<ul><li>
Documentation and Records Management:</li></ul><ul><li>
Accurately and thoroughly document medical notes, patient histories, and examination findings during the patient's visit.</li><li>
Record details of surgical consultations, including pre-operative and post-operative instructions.</li><li>
Maintain patient charts and records, ensuring all entries meet compliance standards.</li></ul>
Communication Support:<ul><li>
Act as a liaison between the physician, patients, and other medical staff.</li><li>
Clarify instructions provided by the physician to the patient and ensure patient understanding.</li><li>
Coordinate communication with external entities, such as pharmacies, labs, or referring physicians.</li></ul>
Preparation and Follow-Up:<ul><li>
Prepare examination rooms, equipment, and instruments prior to patient visits.</li><li>
Assist in retrieving diagnostic results, including imaging or laboratory reports, for physician review.</li><li>
Follow up on physician orders, including referrals or prescription documentation.</li></ul>
Technical Assistance:<ul><li>
Operate electronic health records (EHR) systems to input, retrieve, and manage data.</li><li>
Assist the ophthalmologist during minor in-office procedures by recording notes and providing ancillary support.</li></ul>
Compliance and Confidentiality:<ul><li>
Ensure adherence to HIPAA and other regulatory requirements in maintaining patient confidentiality.</li><li>
Stay updated on industry standards and best practices for medical documentation.</li></ul>
Qualifications:<ul><li>
Education: High school diploma or equivalent required; additional coursework or certification in medical terminology or scribing preferred.</li><li>
Experience: Previous experience in a medical or ophthalmology practice is highly desirable.</li><li>
Skills:<ul><li>
Strong understanding of medical terminology, particularly related to ophthalmology.</li><li>
Proficiency in EHR systems and computer applications.</li><li>
Excellent written and verbal communication skills.</li><li>
Exceptional attention to detail and organizational abilities.</li><li>
Ability to work collaboratively in a fast-paced environment.</li></ul></li></ul>
Work Environment:<ul><li>
Primary work is conducted in an office or clinical setting.</li><li>
Frequent use of computers and medical equipment.</li><li>
Interaction with patients, requiring a professional demeanor and compassionate communication skills.</li></ul>
Physical Requirements:<ul><li>
Ability to sit or stand for extended periods.</li><li>
Manual dexterity to operate office and medical equipment.</li></ul>
This job description is intended to convey information essential to understanding the scope of the position. It is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities, or working conditions associated with the position.</div>

Ophthalmic Scribe - Cumberland-(Must be available to travel to other local clinics)

Care Access

<div><div>About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit www.CareAccess.com.</div><h3 class="jobSectionHeader">
How This Role Makes a Difference</h3>
<div>
Bring clinical research to your community on your schedule.

Join the Future of Medicine program at Care Access, where we're bringing clinical research directly into local communities. As a Clinical Research Assistant, PRN (Registered Nurse) you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life.
</div>
<div><h3 class="jobSectionHeader">How You'll Make An Impact</h3>
<div>
In this event-based role, you'll:
<ul>
<li>Support participant care and event operations, including phlebotomy, specimen handling, and documentation (paper or electronic).</li>
<li>Help set up and manage clinical research events to ensure they run smoothly, safely, and compliantly.</li>
<li>Be part of a mobile, mission-driven team advancing the future of healthcare access.</li>
</ul>
This is not your traditional part-time job. It is flexible, purpose-driven work that fits your schedule. You'll opt into local events through our scheduling system and log actual hours worked after each one. Whether you want to pick up one event a month or several a week, you'll be helping make clinical research more accessible for everyone.
<ul>
<li>Clinical &amp; Participant Care: Perform venipuncture and capillary collections (as applicable) while maintaining aseptic technique and participant comfort. Handle and prepare biospecimens with care &mdash; labeling, processing, packaging, and transferring or shipping under proper chain-of-custody and temperature controls. Communicate clearly and promptly escalate any safety or quality concerns to onsite leadership.</li>
<li>Study Operations &amp; Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA). Follow established SOPs to help keep each event audit-ready and compliant.</li>
<li>Participant Experience &amp; Event Operations: Welcome participants and help guide them through event flow. Set up and break down event stations, prepare kits and supplies, and maintain a safe, organized, and professional workspace that reflects Care Access' high standards.</li>
<li>Site &amp; Administrative Support: Assist with light administrative and inventory tasks that keep the event running smoothly, from restocking supplies to supporting team coordination.</li>
</ul></div><h3 class="jobSectionHeader">The Expertise Required</h3>
<div><ul><li>Clinical Expertise: Proficiency in venipuncture and specimen handling best practices, with strong attention to labeling, documentation, and chain-of-custody integrity.</li>
<li>Participant Care: Clear, compassionate communication skills and professionalism when engaging with participants and community partners.</li>
<li>Tech Readiness: Comfort using mobile apps and e-source tools for real-time logging and documentation.</li>
<li>Dependability &amp; Adaptability: Reliable, punctual, and team-oriented &mdash; able to thrive in dynamic event environments and work independently under event-day guidance.</li>
<li>Mission Mindset (optional addition): Motivated by bringing clinical research to local communities and expanding access to the future of medicine.</li>
</ul></div><div><h3 class="jobSectionHeader">Certifications/Licenses, Education, and Experience</h3>
</div><div><ul><li>Experience: Minimum of 1 year performing phlebotomy and specimen handling activities.</li>
<li>Active, unrestricted RN license in the state of practice.</li>
<li>Active and unrestricted State Board of Nursing license in good standing</li>
</ul></div><h3 class="jobSectionHeader">How We Work Together</h3>
<ul> <li>Location: This is an on-site position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.</li>
<li>Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.
<ul><li>Walking - 20%</li>
<li>Standing - 40%</li>
<li>Sitting - 30%</li>
<li>Lifting (up to 25 lbs., over 25lbs, and overhead) - 10%</li>
<li>Driving - &lt;10%</li>
<li>Exposure to bloodborne pathogens - 50% (variable by station supporting)</li>
</ul>
</li></ul>The expected salary range for this role is $19.00 - $44.00 USD per hour for full time team members.
</div><div>
Diversity &amp; Inclusion

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access is unable to sponsor work visas at this time.

If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com

Mandatory Employer Disclosures: 
Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. 
Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment. 
Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment. 
Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. 
Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29&ndash;38 of Title 28 of the Rhode Island General Laws. 
Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.</div></div>

Clinical Research Assistant, PRN (Registered Nurse)

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