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Clinical Data Coordinator Jobs in Decatur, GA (NOW HIRING)

Artivion

Sr. Clinical Data Manager

Kennesaw, GA · On-site

The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This ...

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This ...

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$15

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$55

How much do clinical data coordinator jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for clinical data coordinator in Decatur, GA is $28.95, according to ZipRecruiter salary data. Most workers in this role earn between $22.31 and $33.08 per hour, depending on experience, location, and employer.

What Does a Clinical Data Coordinator Do?

A clinical data coordinator is responsible for overseeing a number of data related tasks associated with running a clinical facility. In this career, your job duties include creating reports on patient data, developing programs that support a clinical study, and providing information to ensure regulatory compliance on behalf of the clinic. The qualifications needed to have a career as a clinical data coordinator include a bachelor's degree in computer science or a related field. You also need strong analytical skills and experience working with databases.

What are the key skills and qualifications needed to thrive as a Clinical Data Coordinator, and why are they important?

To thrive as a Clinical Data Coordinator, you need strong analytical skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor’s degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory standards such as GCP and FDA guidelines are essential. Excellent organizational skills, effective communication, and the ability to collaborate with multidisciplinary teams help set top candidates apart. These competencies ensure accurate data collection and integrity, which are crucial for the success and compliance of clinical trials.

How does a Clinical Data Coordinator typically collaborate with other teams during a clinical trial?

Clinical Data Coordinators work closely with clinical research associates, data managers, and regulatory teams to ensure the accurate collection and management of trial data. They frequently communicate with site staff to resolve data discrepancies and ensure adherence to protocol and data quality standards. Regular meetings and updates are common to address ongoing data queries, share progress, and align on timelines. This cross-functional collaboration is vital for maintaining the integrity of clinical trial data and supporting successful study outcomes.

What is the difference between Clinical Data Coordinator vs Clinical Research Associate?

AspectClinical Data CoordinatorClinical Research Associate
Primary RoleManage and ensure accuracy of clinical data collection and entryOversee clinical trial sites, monitor study progress, and ensure compliance
Required CredentialsTypically a bachelor's degree in health, life sciences, or related fieldUsually a bachelor's degree in health sciences, along with monitoring certifications
Work EnvironmentData management teams, clinical trial databases, research organizationsClinical sites, monitoring visits, regulatory agencies
Industry UsageCommon in clinical data management and research organizationsCommon in pharmaceutical companies and contract research organizations

The Clinical Data Coordinator focuses on managing and verifying clinical data accuracy, while the Clinical Research Associate monitors trial sites and ensures compliance. Both roles are essential in clinical research but differ in daily responsibilities and focus areas.

More about Clinical Data Coordinator jobs
What are the most commonly searched types of Clinical Data jobs in Decatur, GA? The most popular types of Clinical Data jobs in Decatur, GA are:
What are popular job titles related to Clinical Data Coordinator jobs in Decatur, GA? For Clinical Data Coordinator jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Clinical Data Coordinator jobs in Decatur, GA look for? The top searched job categories for Clinical Data Coordinator jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Data Coordinator jobs? Cities near Decatur, GA with the most Clinical Data Coordinator job openings:
Clinical Data Coordinator jobs near you
Infographic showing various Clinical Data Coordinator job openings in Decatur, GA as of May 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 87% Full Time, 4% Part Time, 1% Temporary, and 6% Contract. Highlights an 93% Physical, 4% Hybrid, and 3% Remote job distribution, with an average salary of $60,207 per year, or $28.9 per hour.
Clinical Research & Data Coordinator

Clinical Research & Data Coordinator

Morehouse School of Medicine

Atlanta, GA • On-site

$23.25 - $31/hr

Full-time

Posted 8 days ago

Job description

Posting Details
Position Information
About MSM
Morehouse School of Medicine (MSM) is a place of distinction, serving as the nation's leading academic medical center for vulnerable populations. It's also a place for passionate individuals looking to join a dedicated community working today to help prepare tomorrow's leaders.
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.
At Morehouse School of Medicine, we're leading the creation and advancement of health equity. You will find a fulfilling career at MSM!
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
Morehouse School of Medicine is seeking a highly motivated, detail-oriented Clinical Research & Data Coordinator to support the Precision Medicine Implementation studies, like the Tulisokibart for Moderate to Severe Ulcerative Colitis Study. This pivotal role is responsible for facilitating the timely and accurate matching of participants to appropriate clinical trials, with an emphasis on leveraging electronic health records (EHRs) for participant identification and data management. The coordinator will oversee key aspects of clinical trial operations and assist with ensuring seamless and secure access to and utilization of clinical data. This includes managing study participant data, preparing for rapid clinical trial study activations, ensuring data integrity, and serving as a liaison between physicians, research teams, and other stakeholders. This position plays a vital role in advancing clinical research and improving patient access to clinical trials.
REPORTS TO: Principal Investigator, Tulisokibart for Moderate to Severe Ulcerative Colitis Study
KNOWLEDGE, SKILLS, & ABILITIES:
  • Strong understanding of clinical research processes and human subjects research and protections.
  • Understanding of clinical data, including data structures, standards, and ontologies29292929.
  • Familiarity with oncology trials and precision medicine concepts, particularly related to genomic testing and clinical trial matching.
  • Working knowledge of electronic health records (EHRs), clinical trial management systems (CTMS), and data entry protocols.
  • Awareness of ethical considerations related to the informed consent process and data privacy33. Also, familiarity with regulatory and ethical aspects of clinical research, including Good Clinical Practice (GCP) guidelines, Institutional Review Board (IRB) procedures, and Health Insurance Portability and Accountability Act (HIPAA) regulations.
  • Ability to build and maintain positive working relationships across interdisciplinary teams.
  • Ability to adapt quickly to changes in program needs, study protocols, and technology platforms.
  • Ability to manage multiple tasks and projects simultaneously, set priorities, and meet deadlines.
  • Ability to maintain confidentiality and protect sensitive patient and research data, upholding ethical standards and complying with all regulations applicable to clinical research.

CORE COMPETENCIES:
  1. Clinical Research Coordination: Understands clinical trial protocols, workflows, and regulatory compliance and coordinates multiple study components with precision and timeliness.
  2. Attention to Detail: Demonstrates accuracy in data entry, documentation, and review; identifies and resolves discrepancies in patient records and study data.
  3. Communication: Communicates clearly and effectively with internal and external stakeholders, including physicians, patients, and research staff, adapting messaging based on the audience and context (e.g., written, verbal, or electronic).
  4. Collaboration & Teamwork: Builds productive relationships across departments and with partner organizations and demonstrates a cooperative approach and willingness to support team goals.
  5. Patient-Centered Focus: Prioritizes patient safety, privacy, and access to appropriate clinical trials and demonstrates cultural sensitivity and empathy in patient interactions.
  6. Problem-Solving & Critical Thinking: Identifies operational challenges and proposes practical, evidence-based solutions; anticipates potential issues and takes proactive steps to minimize disruptions.
  7. Time Management & Adaptability: Manages shifting priorities in a dynamic research environment and remains flexible and calm under pressure, especially during rapid study activations.
  8. Ethical Conduct & Integrity: Upholds institutional and regulatory standards related to clinical research and handles confidential data responsibly, and adheres to ethical principles.
  9. Technology Proficiency: Navigates clinical databases, electronic health records (EHRs), and research software efficiently and learns new digital tools and platforms as needed for trial coordination.
  10. Project Management: Demonstrates experience in coordinating and managing projects, ensuring objectives are met within set timeframes. Able to identify and allocate resources effectively and can anticipate and mitigate potential risks or delays.

SUPERVISORY RESPONSIBILITIES:
This position will not have any supervisory responsibilities.
Minimum Qualifications
Education
High School Diploma or GED and three years of clinical research experience. OR Two years of college in a scientific, health-related, or business administration program and one year of clinical research experience. OR Licensed as a practical nurse (LPN) and with one year of clinical research experience. OR Bachelor's degree, Master's degree, MD or PhD in a scientific, health-related or business administration program.
Experience
Minimum 2-3 years of experience working with clinical data, particularly in a research or healthcare setting.
MS Office Suite.
Ability to prioritize tasks and work independently, as well as part of a multi-disciplinary team.
Preferred Qualifications
Familiarity with EHR data standards, data integration, and the ethical/legal considerations surrounding data usage.
Excellent analytical, problem-solving, and organizational skills.
Superior communication skills, both written and verbal.
MS Office Suite.
Closing Date
Open Until Filled
Yes
Special Instructions to Applicants
Employment in this role may be contingent upon extramural funding and successful performance and may be terminated or reduced in percentage of appointment if such funding is not secured or ceases to be available.
Quick Link
https://careers.msm.edu/postings/24091
EEO Statement Summary
Morehouse School of Medicine is an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all Federal and Georgia State laws, regulations, and executive orders regarding non-discrimination and affirmative action. Morehouse School of Medicine does not discriminate on the basis of race, age, color, religion, national origin or ancestry, sex, gender, disability, veteran status, genetic information, sexual orientation, or gender identity or expression.
Job Duties
Description of Job Duty
POSITION ACCOUNTABILITIES AND ESSENTIAL FUNCTIONS:
Study Participant Management: Oversee the electronic health records (EHRs) to identify & match study participants and screen and enroll study participants for available clinical trials.
  1. Clinical Data Management: Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture (EDC) systems and in a timely manner, adhering to established protocols and guidelines.
  2. Study Coordination: Collaborate with researchers and physicians to implement health informatics solutions that support the enrollment of clinical trial participants.
  3. Study Compliance and Data Integrity: Maintain data standards, ontologies, and metadata frameworks in alignment with best practices and regulatory requirements. Ensure adherence to clinical trial regulatory requirements (IRB, HIPAA, GCP, etc.).
  4. Data Analysis: Assist with data visualization and communication of clinical and real-world data to various stakeholders.
  5. Collaboration: Contribute to the drafting of manuscripts, reports, and grants, as well as present findings at scientific meetings and conferences.

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