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Associate Clinical Data Manager Jobs in Powder Springs, GA

Pwc

Data Strategy-Manager

Atlanta, GA · On-site

$99K - $232K/yr

Industry/Sector Not Applicable Specialism Data, Analytics & AI Management Level Manager & Summary ... Associate - SAP Master Data Governance (MDG) - SnowPro Core / SnowPro Advanced - Databricks ...

Milliman

Strategic Data Partnership Manager

Atlanta, GA · Remote

Manage relationships with current data and technology partners -- ensuring they remain productive ... Assess gaps in our data offerings (SDoH, clinical depth, novel real-world sources, etc.), evaluate ...

HD Supply

Manager, Data Analytics

Atlanta, GA · On-site

3+ year experience 1+ years experience managing teams 3+ years experience Pricing & Sales Job ... Supply associate. We value the diversity of our people. Equal Employment Opportunity HD Supply is ...

HD Supply

Manager, Data Analytics

Atlanta, GA · On-site

3+ year experience 1+ years experience managing teams 3+ years experience Pricing & Sales Job ... Supply associate. We value the diversity of our people. Equal Employment Opportunity HD Supply is ...

Pwc

Data Governance- Manager

Atlanta, GA · On-site

$99K - $232K/yr

Industry/Sector Not Applicable Specialism Data, Analytics & AI Management Level Manager & Summary ... Associate - SAP Master Data Governance (MDG) - SnowPro Core / SnowPro Advanced - Databricks ...

Mirus LLC

Clinical Specialist

Marietta, GA · On-site

You are the TAVR expert in interpreting clinical data relating to the treatment options for specific patients. * OR/Cath Lab management: In the Cath lab/OR, you provide support during the procedure ...

Mirus LLC

Clinical Specialist

Marietta, GA · On-site

You are the TAVR expert in interpreting clinical data relating to the treatment options for specific patients. * OR/Cath Lab management: In the Cath lab/OR, you provide support during the procedure ...

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Showing results 21-40

All JobsAssociate Clinical Data JobsAssociate Clinical Data Manager JobsAssociate Clinical Data Manager Jobs in Powder Springs, GA

Associate Clinical Data Manager information

See Powder Springs, GA salary details

$13

$36

$82

How much do associate clinical data manager jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for associate clinical data manager in Powder Springs, GA is $36.88, according to ZipRecruiter salary data. Most workers in this role earn between $27.79 and $36.88 per hour, depending on experience, location, and employer.

What does an associate clinical data manager do?

An Associate Clinical Data Manager is responsible for collecting, cleaning, and managing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They work closely with clinical teams to design data collection tools, monitor data quality, and resolve discrepancies. Their work is crucial in supporting the analysis and reporting of clinical trial results, which can impact decisions about new medical treatments.

What are the key skills and qualifications needed to thrive as an associate clinical data manager?

To thrive as an Associate Clinical Data Manager, you need a solid background in life sciences or related fields, strong analytical abilities, and attention to detail, often supported by a relevant bachelor's degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools like Medidata Rave, and an understanding of regulatory guidelines such as ICH-GCP are typically required. Excellent organizational skills, effective communication, and problem-solving abilities help you excel in managing complex datasets and collaborating across teams. These skills ensure data integrity, regulatory compliance, and smooth conduct of clinical trials, which are critical to successful drug development.

What are some common challenges an associate clinical data manager might face when working on multi-site clinical trials?

Associate Clinical Data Managers often encounter challenges such as ensuring data consistency across different trial sites and managing discrepancies that arise from varying data entry practices. Coordinating with site staff, monitoring data quality, and adhering to strict timelines require strong communication and organizational skills. Additionally, adapting to evolving regulatory requirements and new data management technologies can be demanding, but these challenges also offer valuable learning opportunities for career growth.
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Associate Clinical Data Manager jobs near you
Infographic showing various Associate Clinical Data Manager job openings in Powder Springs, GA as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, and 3% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $76,720 per year, or $36.9 per hour.

Clinical Research & Data Coordinator

Morehouse School of Medicine

Atlanta, GA • On-site

$23.25 - $31/hr

Full-time

Re-posted 18 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
NONAC3730
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
The GRAIL Pathfinder II study team at the Morehouse School of Medicine is seeking a passionate and dedicated Community Outreach Coordinator/Navigator. The candidate will play a crucial role in bridging the gap between the study team and community clinics, churches, and other healthcare organizations. Expertise in identifying and engaging community leaders, including clinicians, church officials, and patient navigators, to facilitate and enhance the reach and impact of the study will be key.
POSITION ACCOUNTABILITIES AND ESSENTIAL FUNCTIONS:
  1. Study Participant Management: Oversee the electronic health records (EHRs) to identify & match study participants and screen and enroll study participants for available clinical trials.
  2. 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 promptly, adhering to established protocols and guidelines.
  3. Study Coordination: Collaborate with researchers and physicians to implement health informatics solutions that support the enrollment of clinical trial participants.
  4. 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.).
  5. Data Analysis: Assist with data visualization and communication of clinical and real-world data to various stakeholders.
  6. Collaboration: Contribute to the drafting of manuscripts, reports, and grants, as well as present findings at scientific meetings and conferences.

Reporting & Documentation:
  • Maintain detailed records of outreach activities, including meetings, interactions, and outcomes.
  • Prepare regular reports detailing outreach efforts, challenges, and opportunities for the leadership team.

KNOWLEDGE, SKILLS, & ABILITIES:
  • Comprehensive knowledge of local community dynamics, culture, and key stakeholders.
  • Strong organizational skills with the ability to multitask and manage multiple projects simultaneously.
  • Proficient communication skills, both written and verbal, with the ability to engage diverse audiences.
  • Familiarity with healthcare or academic research settings is an advantage.

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.

Minimum Qualifications
  1. Minimum 2-3 years of experience working with clinical data, particularly in a research or healthcare setting.
  2. Familiarity with EHR data standards, data integration, and the ethical/legal considerations surrounding data usage.
  3. Excellent analytical, problem-solving, and organizational skills.
  4. Superior communication skills, both written and verbal.
  5. Ability to prioritize tasks and work independently, as well as part of a multi-disciplinary team.
  6. Prior experience in health-related community outreach and event organization is highly preferred.

Preferred Qualifications
  1. Experience in public health, communications, social work, or a related field.
  2. Intermediate or higher proficiency in MS Office Suite.
  3. Strong knowledge of the local community, culture, and key stakeholders.
  4. Excellent communication, interpersonal, and organizational skills.
  5. Ability to work independently and collaboratively in a team-oriented environment.

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/24113
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
The GRAIL Pathfinder II study team at the Morehouse School of Medicine is seeking a passionate and dedicated Community Outreach Coordinator/Navigator. The candidate will play a crucial role in bridging the gap between the study team and community clinics, churches, and other healthcare organizations. Expertise in identifying and engaging community leaders, including clinicians, church officials, and patient navigators, to facilitate and enhance the reach and impact of the study will be key.
POSITION ACCOUNTABILITIES AND ESSENTIAL FUNCTIONS:
Community Engagement:
  • Identify and coordinate meetings between study staff and influential community (healthcare, churches, health promotion organizations, etc.) authorities and stakeholders, including but not limited to clinic administrators, physicians, church leaders.
  • Develop and nurture relationships with various community entities to bolster the study's visibility and engagement.

Event Organization:
  • Plan, organize, and execute community events to inform and enroll participants in the GRAIL Pathfinder II study.
  • Coordinate logistics, materials, and communication for successful event execution.

Communication & Collaboration:
  • Work closely with the principal investigator and associate director to formulate outreach strategies.
  • Provide regular updates and feedback, ensuring alignment with the study's objectives and guidelines.

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, 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.

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