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Data Coordinator Jobs in Decatur, GA (NOW HIRING)

Immediate Position Overview We are seeking an experienced Project Coordinator to support a large-scale data center project currently underway in the Atlanta market. This role will focus heavily on ...

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Project Coordinator

Atlanta, GA ยท On-site

$25 - $35/hr

Immediate Position Overview We are seeking an experienced Project Coordinator to support a large-scale data center project currently underway in the Atlanta market. This role will focus heavily on ...

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The Data & Evaluation Coordinator serves as a key contributor to organizational learning, quality assurance, and evidence-informed decision-making. In partnership with the Senior Director of Outcomes ...

HDR Engineering is currently seeking a Data Center Substation Coordinator to join our growing and nationally ranked team of Power Delivery professionals. * Responsibilities include: * Work under the ...

HDR Engineering is currently seeking a Data Center Substation Coordinator to join our growing and nationally ranked team of Power Delivery professionals. * Responsibilities include: * Work under the ...

HDR Engineering is currently seeking a Data Center Substation Coordinator to join our growing and nationally ranked team of Power Delivery professionals. * Responsibilities include: * Work under the ...

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Data Coordinator information

See Decatur, GA salary details

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How much do data coordinator jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for data coordinator in Decatur, GA is $26.10, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $30.05 per hour, depending on experience, location, and employer.

What skills do you need to be a data coordinator?

A data coordinator needs strong organizational skills, attention to detail, and proficiency in data management tools such as Excel, SQL, or database software. Good communication skills and the ability to analyze and interpret data are also important for ensuring data accuracy and supporting decision-making.

What are some typical challenges a Data Coordinator might face when managing large datasets across multiple departments?

A common challenge for Data Coordinators is ensuring data consistency and accuracy when consolidating information from various departments, each potentially using different systems or formats. This often requires strong attention to detail, proactive communication, and the ability to create or enforce standardized data entry protocols. Additionally, Data Coordinators may need to troubleshoot discrepancies quickly and collaborate closely with IT teams or department leads to resolve issues and streamline workflows.

How much does a data coordinator make?

The average salary for a data coordinator in Texas is approximately $50,000 to $65,000 per year, depending on experience, industry, and certifications. Entry-level positions may start around $45,000, while experienced coordinators can earn over $70,000. Skills in data management tools like Excel, SQL, or data visualization software can influence salary levels.

Is a coordinator a higher position than a manager?

In most organizational structures, a manager typically holds a higher position than a coordinator, as managers oversee teams and make strategic decisions, while coordinators handle specific tasks and support roles. However, titles and hierarchy can vary by company, so it's important to review the specific job descriptions and organizational charts.

What does a Data Coordinator do?

A Data Coordinator is responsible for managing, organizing, and maintaining data for an organization. They ensure data accuracy, integrity, and accessibility, often by collecting information, entering it into databases, and performing regular data quality checks. Data Coordinators may also generate reports, assist with data analysis, and support other teams by providing up-to-date information. Their work is essential for informed decision-making and efficient operations within a company.

What is the role of a data coordinator?

A data coordinator is responsible for managing, organizing, and maintaining data within an organization. They ensure data accuracy, integrity, and security, often using database tools and software, and may collaborate with other teams to support data-driven decision-making.

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

To thrive as a Data Coordinator, you need strong organizational skills, attention to detail, and experience with data entry and management, often supported by a degree in information management or a related field. Proficiency in database software, Excel, and data visualization tools, as well as familiarity with data privacy regulations, is typically required. Excellent communication, problem-solving, and time management skills help you collaborate effectively and ensure data accuracy. These skills are essential for maintaining reliable data systems and supporting informed decision-making within organizations.
What are the most commonly searched types of Data jobs in Decatur, GA? The most popular types of Data jobs in Decatur, GA are:
What are popular job titles related to Data Coordinator jobs in Decatur, GA? For Data Coordinator jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Data Coordinator jobs in Decatur, GA look for? The top searched job categories for Data Coordinator jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Data Coordinator jobs? Cities near Decatur, GA with the most Data Coordinator job openings:
Infographic showing various Data Coordinator job openings in Decatur, GA as of June 2026, with employment types broken down into 1% Internship, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $54,291 per year, or $26.1 per hour.
Clinical Research & Data Coordinator

Clinical Research & Data Coordinator

Morehouse School of Medicine

Atlanta, GA โ€ข On-site

$23.25 - $31/hr

Full-time

Posted 25 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:
โ€ข Improve the health and well-being of individuals and communities;
โ€ข Increase the diversity of the health professional and scientific workforce;
โ€ข 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.