678 Results for

Clinical Jobs in Tucker, GA

Jobs

Stockbridge, GA

$100,000–$125,000 / year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. A growing, clinician-led ABA organization in the greater Atlanta area is seeking an experienced Clinical Director / BCBA to lead a center-based program in Stockbridge, GA.

6 days ago

Smyrna, GA

$100,000–$130,000 / year

The Clinical Director will partner closely with executive leadership to drive clinical excellence, improve operational outcomes, mentor BCBA Supervisors, and support the continued expansion of services to families across assigned regions. We are a rapidly growing, BCBA-founded ABA organization committed to delivering compassionate, outcomes-driven autism services across center-based, home-based, school, and community settings.

4 days ago

Atlanta, GA

$42–$42

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Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant's goals and values.

Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career!

1 day ago

Sandy Springs, GA

$45–$55.55 / hour

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Our programs are designed to support working adults, with a strong emphasis on hands-on learning, clinical partnerships, and career readiness.

3 days ago

Sandy Springs, GA

$90,000–$110,000 / year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners.

4 days ago

Decatur, GA

As the facility leader, you will be part of a close-knit, collaborative team responsible for delivering unique care plans and providing dialysis treatment to patients facing end stage renal disease or chronic kidney disease. We have a diverse range of employee resource groups (ERGs) to encourage employees with similar interests, goals, social and cultural backgrounds, or experiences to come together for professional and personal development, discussion, activities, and peer support.

2 days ago

Conyers, GA

Serves as part of the entity management team and Shared Governance Model focused on promoting the mission, vision and values, of PHC and Nursing Professional Practice, embracing a person-centered philosophy while promoting patient- family centered services across the continuum and enhancing value-driven outcomes.

Overview: Administrative and operational responsibility for assigned departments, including management of cost and finance, human resources, operations, quality of care and clinical outcomes, patient/physician and staff satisfaction, change management and any other relevant responsibilities related to this position.

12 days ago

Roswell, GA

Act as QAPI (Quality Assessment and Performance Improvement) owner; participate in QA activities, investigate incidents, analyze trends, and implement corrective actions. Provide training, supervision, coaching, and mentoring to clinicians (including contract staff); assign patients/staff based on competence.

5 days ago

Atlanta, GA

$88,000–$163,000

Our passionate, global workforce augments local expertise and diverse mix of skills with data, science, and technology to deliver bespoke engagement solutions that help clients reimagine how they engage with their patients, payers, people, and providers to improve treatment outcomes.

Job Description

Inizio Engage has a long-standing partnership with a leading biotechnology organization across Commercial, Patient Solutions and Medical Affairs businesses.

Today

Decatur, GA

Part time

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Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.

30+ days ago

Decatur, GA

Part time

Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.

Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.

2 days ago

Kennesaw, Georgia

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2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures.

Provides relevant information regarding the projected regional costs of treatments, projected enrollment capabilities, anticipated risks/benefits at specific study sites, logistical impediments, etc. for use in study contract and budget negotiations.

10 days ago

Decatur, GA

Part time

Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.

Obtains samples per protocol, performs select diagnostic test or limited high complexity testing and documents process in source documents.

30+ days ago

Marietta, GA

p>Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents. The role will assist with the management of cardiovascular clinical studies for MiRus products, with a focus on meeting critical timelines, developing high-quality documentation, and ensuring accurate data collection.

30+ days ago

Marietta, GA

Remote

Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager.

30+ days ago

Marietta, GA

Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager.

30+ days ago

Atlanta, Georgia

The IS Epic Application Manager represents the Information Systems team and is responsible for establishing and maintaining strong working relationships with Shepherd Center staff, our Community Connect partner (Piedmont Healthcare), Epic representatives, and all users who interact with Epic applications. With five decades of experience, Shepherd Center provides world-class clinical care, research, and family support for people experiencing the most complex conditions, including spinal cord and brain injuries, multi-trauma, traumatic amputations, stroke, multiple sclerosis, and pain.

30 days ago

Atlanta, Georgia

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Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner.

4 days ago

Forest Park, Georgia

Clinical Research Management, Clinical Study Protocols, Database Management, Data Entry, Detail-Oriented, Freezerworks (Software), Ordering Supplies, Organizing, Participant Recruiting, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS), Team Supervision, Written Communication

Grade. This person will oversee and coordinate complex or multi-site clinical research studies, serve as a resource to provide comprehensive information to clinical research staff, promote smooth clinical operations, prepare regulatory compliance documents, coordinate interaction with other departments, and supervise clinical research coordinators and staff.

Job Description.

30+ days ago

Lawrenceville, GA

li>If not Certified Clinical Research Coordinator (CCRC) or a Certified Clinical Research Professional (CCRP) at time of hire, must achieve professional certification through the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA) within three (3) years of hire.

Master of Science degree from an accredited college or university in a data driven research-related field (such as nursing, allied health, biological sciences, chemistry, economics, informatics, mathematics, psychology, sociology, epidemiology, public health).

30+ days ago

Lilburn, Georgia

Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits.

20 days ago

Remote

$97,000–$193,000 / year

li>

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

16 days ago

Remote

$97,000–$193,000 / year

18 days ago

Atlanta, GA

Cancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient's needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer.

Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia's only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.

30+ days ago

Atlanta, Georgia

Cancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient’s needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer.

Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia’s only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.

30+ days ago

Atlanta, GA

$19–$44 / hour

p>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.

Study Operations & 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).

20 days ago

Atlanta, GA

$34–$44 / hour

Study Operations & 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).

20 days ago

Atlanta, GA

Logs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe. " Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).

30+ days ago

Atlanta, GA

This pivotal role is responsible for facilitating the timely and accurate data analysis of participants to appropriate clinical trials, with an emphasis on leveraging electronic health records (EHRs) for participant identification and data management, formulation, and preparation of official institutional information to internal and/or external parties. Formulate and prepare official institutional information to internal and/or external queries and requests for institutional data and statistics on a wide range of issues, including university information, student characteristics (enrollment, degrees, retention, etc.), faculty characteristics, employment/benefits, financial information, and projections.

30+ days ago

Decatur, Georgia

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30+ days ago

Woodstock, GA

Responsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and. Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.

30+ days ago

Decatur, Georgia

Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.

30+ days ago

Decatur, GA

Part time

Working closely with clinical operations, data management, and regulatory teams, the QC Associate reviews essential trial documents and clinical data to verify compliance with GCP (Good Clinical Practice), ICH guidelines, regulatory requirements, and internal SOPs.

Performs quality control reviews of clinical trial documents (e.g., informed consent forms, case report forms, regulatory binders, monitoring visit reports) to ensure accuracy, completeness, and consistency.

2 days ago

Decatur, GA

Responsibilities may include but are not limited to: • Screening of patients for study enrollment • Patient consents • Patient follow-up visits • Documenting in source clinic charts • Entering data in EDC and answering queries • Obtaining vital signs and ECGs • May perform basic lab procedures per protocol such as blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens, and notification of courier for specimen pick-up • Requesting and tracking medical record requests • Updating and maintaining logs, chart filings • Maintaining & ordering study specific supplies • Scheduling subjects for study visits and conducts appointment reminders • Building, updating source as needed • Conducting monitoring visits and resolves issues as needed in a timely manner • Ensuring study related reports and patient results are reviewed by investigator in a timely manner • Filing SAE • Deviation reports to Sponsor and IRB as needed • Documenting and reporting adverse events • Reporting non-compliance to appropriate staff in timely manner • Maintaining positive and effective communication with clients and team members • Always practicing ALCOA principles with all documentation • May assist with study recruitment, patient enrollment, and tracking as needed • Maintaining confidentiality of patients, customers, and company information • Performing all other duties as requested or assigned • Complete all needed activities for study start-up including completing required training, uploading printing certificates to file in ISF, etc.

• Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently 40 wpm • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc.

30+ days ago

Atlanta, GA

With five decades of experience, Shepherd Center provides world-class clinical care, research, and family support for people experiencing the most complex conditions, including spinal cord and brain injuries, multi-trauma, traumatic amputations, stroke, multiple sclerosis, and pain. Job Responsibilities: Evaluates patients speech, language, cognitive, and swallowing abilities and develops a Plan Of Care that is individualized towards the patients cognitive-linguistic and/or swallowing capabilities to maximize their functional independence and safety.

30+ days ago

Monitor and review study budget and data management activities, such as PRF development, training, and facilitating query resolution with proper documentation • Support monitoring efforts by setting quality and compliance goals by overseeing and approving study monitoring plans, may review, suggest edits and approve monitoring trip reports • Contribute to contract review and negotiations with outside vendors and study sites or laboratories • Mentor CTMs and CRAs • Demonstrate an ability to influence others to achieve positive results and collaboration through diplomacy and respect for others, appropriate prioritization and facilitation of the decision-making process Qualifications Qualifications: • Bachelors degree or higher, or equivalent credentials • Knowledge of GCP, ICH guidelines, and other clinical regulatory requirements • Strong interpersonal skills (verbal and written), organizational, and prioritization skills, able to communicate at multiple levels of an organization and with sponsors/clients. Primary Responsibilities (all levels): • Manage, design and implement all clinical operational aspects of IVD clinical trials from inception through close-out • Serve as main point of contact for internal and external study stakeholders; effectively communicating, collaborating, managing escalation of issues, where necessary, as well as participating and leading internal and external study meetings • Identify, evaluate, and oversee qualification and contracting for study investigators, study sites, CRO and/or vendor management for the study, where applicable • Develop or assist in the development of study-related plans and documents including protocols, informed consent forms, monitoring plans, case report forms, training plans and engagement materials • Ensure trial master file (TMF/eTMF) is established, current, and maintained per ICH E6.

30+ days ago

Decatur, Georgia

Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.

Obtains samples per protocol, performs select diagnostic test or limited high complexity testing and documents process in source documents.

30+ days ago

Decatur, GA

li>Scheduling subjects for study visits and conducts appointment reminders;

Building/updating source as needed;

Conducting monitoring visits and resolves issues as needed in a timely manner;

Ensuring study related reports and patient results are reviewed by investigator in a timely manner;

Filing SAE/Deviation reports to Sponsor and IRB as needed;

Documenting and reporting adverse events;

Reporting non-compliance to appropriate staff in timely manner;

Maintaining positive and effective communication with clients and team members;

Always practicing ALCOAC principles with all documentation;

May assist with study recruitment, patient enrollment, and tracking as needed;

Maintaining confidentiality of patients, customers and company information, and;

Performing all other duties as requested or assigned. Responsibilities may include but are not limited to:

Screening of patients for study enrollment;
Patient consents;
Patient follow-up visits;
Documenting in source clinic charts;
Entering data in EDC and answers queries;
Obtaining vital signs and ECGs;
May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
Requesting and tracking medical record requests;
Updating and maintaining logs, chart filings;
Maintaining & ordering study specific supplies;].

30+ days ago

Atlanta, GA

p>Perform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.

30+ days ago

Atlanta, Georgia

With five decades of experience, Shepherd Center provides world-class clinical care, research, and family support for people experiencing the most complex conditions, including spinal cord and brain injuries, multi-trauma, traumatic amputations, stroke, multiple sclerosis, and pain. An elite center ranked by" U.S. News "as one of the nation's top hospitals for rehabilitation, Shepherd Center is also recognized as both Spinal Cord Injury and Traumatic Brain Injury Model Systems.

30+ days ago

Atlanta, Georgia

With five decades of experience, Shepherd Center provides world-class clinical care, research, and family support for people experiencing the most complex conditions, including spinal cord and brain injuries, multi-trauma, traumatic amputations, stroke, multiple sclerosis, and pain. An elite center ranked by" U.S. News "as one of the nation's top hospitals for rehabilitation, Shepherd Center is also recognized as both Spinal Cord Injury and Traumatic Brain Injury Model Systems.

30+ days ago

Atlanta, GA

$19–$44 / hour

p>Study Operations & 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). As a Clinical Research Assistant, PRN, 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.

30+ days ago

Atlanta, GA

$19–$44 / hour

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. Walking - 20% Standing - 40% Sitting - 30% Lifting (up to 25 lbs., over 25lbs, and overhead) - 10% Driving - <10% Exposure to bloodborne pathogens - 50% (variable by station supporting).

30+ days ago

Atlanta, GA

Posting Number NONAC3723 Job Title Clinical Research & Data Coordinator Position Title Clinical Research & Data Coordinator Position Type Non-Faculty Number of vacancies 1 Salary Commensurate with experience Department Cancer Health Equity Institute Position Summary. We exist to: Improve the health and well-being of individuals and communities; Increase the diversity of the health professional and scientific workforce; Address primary health care through programs in education, research and service; With emphasis on people of color and the under-served urban and rural populations in Georgia, the nation and the world.

30+ days ago

Atlanta, Virginia

Applicants who require accommodation to participate in the job application process should submit the following form: Accessibility Accommodation Request Form and a member of the team will be in contact.

Prospective employees required to be screened under Florida law should review the education and awareness resources at HB531 | Florida Agency for Health Care Administration.

5 days ago

Atlanta, GA

Remote

To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD).

Performs patient evaluations, administers medications and research instruments and provides nursing support to perform specialized diagnostic, therapeutic and surgical procedures.

15 days ago

Atlanta, Georgia

Discover Your Career at Emory University:

Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future.

Performs patient evaluations, administers medications and research instruments and provides nursing support to perform specialized diagnostic, therapeutic and surgical procedures.

16 days ago

Decatur, GA

$60,000–$90,000 / year

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. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

30+ days ago

Atlanta, Georgia

Discover Your Career at Emory University:

Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future.

ADDITIONAL JOB DETAILS:

Provides leadership and oversight of significant clinical research project(s) with an emphasis on managing, evaluating and training research staff.

30+ days ago

Atlanta, GA

Remote

li>Or master''s degree, MD or PhD in a scientific, health related, or business administration program and two years of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD).

17 days ago

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Clinical Jobs in Tucker, GA

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Registered Dietitian Clinical Research - PRN Professional Case Management

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Dialysis Clinical Manager Registered Nurse - RN Fresenius Medical Care

Clinical Manager - ICU Piedmont Healthcare

RN Territory Clinical Manager, Home Health Gables Search Group

Clinical Educator Inizio Engage

Clinical Research RN CenExel IResearch LLC

Clinical Research Coordinator CenExel IResearch LLC

Float Clinical Research Coordinator II Fresenius Medical Care

Clinical Research Laboratory Technician CenExel IResearch LLC

In-house Clinical Research Associate (CRA) - Cardiovascular Medical Device MiRus LLC

Clinical Research Associate (CRA) - Cardiovascular Medical Device MiRus LLC

Clinical Trial Manager - Cardiovascular Medical Device MiRus LLC

Epic Clinical Applications Manager Shepherd Center

Registered Dietitian Clinical Research - PRN Act for Health

Clinical Research Coordinator III - Psychiatry Washington University in St Louis

Job Description.

Cardiology Clinical Research Nurse - Gwinnett hub Northside Hospital Inc

Clinical Research Coordinator, On-site, Lilburn, GA IQVIA

Senior Clinical Research Associate - Cardio - East Coast - Remote Worldwide Clinical Trials Holdings Inc

Senior Clinical Research Associate - CNS/Psychiatry - East Coast - Remote Worldwide Clinical Trials Holdings Inc

Assistant Director, Clinical Research Staff Winship Cancer Institute Emory University

Assistant Director, Clinical Research Staff- Winship Cancer Institute Emory University

Clinical Research Assistant, PRN (Phlebotomist, LVN or Registered Nurse) Care Access

Clinical Research Assistant, PRN Care Access

Clinical and Health - Clinical Research Coord II Mindlance

Clinical Research and Data Coordinator Morehouse School of Medicine

Clinical Research RN CenExel

Clinical Research Assistant/ Certified Medical Assistant Alcanza Clinical Research LLC

Clinical Research Coordinator CenExel

Clinical Research Quality Control Associate CenExel IResearch LLC

Clinical Research Coordinator Alcanza Clinical Research LLC

Speech and Language Pathology Clinical Fellow Shepherd Center

Sr. Clinical Trials Manager Agilent Technologies Inc

Clinical Research Laboratory Technician CenExel

Clinical Research Coordinator Alcanza Clinical Research

Clinical Research Coordinator I Ora Inc

Outpatient Clinical Neuropsychologist (Pathways) Shepherd Center

Inpatient Clinical Neuropsychologist - Acquired Brain Injury Shepherd Center

Clinical Research Assistant, PRN Care Access Research LLC

Clinical Research Assistant, PRN Registered Nurse Care Access Research LLC

Clinical Research & Data Coordinator Morehouse School of Medicine

Clinical Provider Auditor II - Payment Integrity SIU Elevance Health

Clinical Research Nurse II | School of Medicine Pediatrics, Infectious Disease Emory University

Clinical Research Nurse II | School of Medicine - Pediatrics, Infectious Disease Emory University

Clinical Research Coordinator II Care Access Research LLC

Clinical Trials Manager - School of Medicine, Emergency Medicine Emory University

Clinical Research Coordinator IV School of Medicine Orthopaedics Emory University

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