17 clinical study coordinator jobs at 5 companies in Atlanta, GA
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Clinical Study Coord
Duarte or Los Angeles or Orange County or Atlanta or Chicago or Phoenix
OnsiteFull Time
2+ YOEBachelor's in science/health preferred (substitutable by additional experience). Minimum 2 years research or clinical experience. Must obtain ACRP or SOCRA within 1 year; IATA, GCP, HSP, and BLS within 1 month. Understand/apply FDA, OHRP, GCP/ICH, HIPAA; execute protocols; coordinate recruitment/consent; monitor participants and report adverse even...
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Clinical Trials Coordinator
Atlanta, Georgia, United States
OnsiteFull Time
3+ YOERequires a bachelor's degree, 3 years of clinical experience, and knowledge of clinical studies, research principles, methodologies, and study design. ACRP/CRA/CCRC or SOCRA/CCRP and CITI training are required.
spreadsheets, databases, Trial Master File (TMF)
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Clinical Research Coordinator II - School of Medicine Neurology
Atlanta, Georgia, United States
OnsiteFull Time
1+ YOECoordinate clinical trial operations including recruitment, study visits, data collection, biospecimen processing, regulatory submissions; requires clinical research experience and relevant certifications.
REDCap
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Clinical Research Coordinator II- School of Medicine, Infectious Diseases
Decatur, Georgia, United States
HybridFull Time
1+ YOECoordinates clinical trial activities, manages study databases, consents participants, prepares regulatory submissions; requires relevant clinical research experience and appropriate credentialing for clinical tasks.
3w
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Clinical Research Coordinator I - School of Medicine, Urology
Atlanta, Georgia, United States
HybridFull Time
Coordinate clinical trial activities, maintain research data and regulatory records, assist with recruitment, collect specimens (including phlebotomy), and manage study logistics; minimum administrative or clinical training as listed.
1mo
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Clinical Research Coordinator II- School of Medicine, Infectious Diseases
Decatur, Georgia, United States
HybridFull Time
Coordinates clinical trial activities, manages study databases and regulatory submissions, obtains consent, supervises specimen collection; requires relevant clinical research experience and completion of clinical researcher credentialing.
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Clinical Research Coordinator II- School of Medicine, Hope Clinic
Decatur, Georgia, United States
HybridFull Time
1+ YOECoordinate clinical trials: manage study databases, consent participants, supervise specimen collection, ensure protocol compliance, prepare regulatory submissions; requires clinical research experience and relevant education or licensure.
3w
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Clinical Research Coordinator II- Winship Cancer Institute
Atlanta, Georgia, United States
OnsiteFull Time
1+ YOEManage clinical trial administration, consent participants, maintain study documentation, prepare regulatory submissions; requires clinical research experience and relevant college degree or equivalent experience.
3w
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Clinical Research Coordinator I- School of Medicine, Kaplan Speech EMA
Atlanta, Georgia, United States
HybridPart Time
3+ YOECoordinate clinic-based EMA research, manage study data, recruit and consent participants, collect specimens (may include phlebotomy), and track regulatory submissions. Requires residency in GA.
Fabla
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Clinical Research Coordinator I- School of Medicine, Infectious Diseases (Hope Clinic)
Decatur, Georgia, United States
HybridFull Time
1+ YOECoordinate clinical trials, maintain study data, assist with recruitment, collect and process specimens; requires relevant college degree or 1–3 years administrative/research experience; residency in GA.
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Clinical Research Coordinator II- Winship Cancer Institute
Atlanta, Georgia, United States
OnsiteFull Time
Requires clinical research experience (various education/experience combinations accepted: HS +5yrs, 2yrs college +3yrs, LPN +2yrs, Bachelor's +1yr, or advanced degree). Responsible for managing study databases, consenting participants, specimen processing, and regulatory submissions.
1mo
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Clinical Research Coordinator II- School of Medicine, Hope Clinic
Decatur, Georgia, United States
HybridFull Time
5+ YOEClinical research experience (various education/experience pathways from HS+5yrs to Master's/MD/PhD), ability to manage study databases, consent participants, prepare regulatory submissions, clinical training via Emory Healthcare, and residency in Georgia.
2w
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Clinical Research Coordinator I - The School of Nursing - Alzheimer's Disease Prevention
Atlanta, Georgia, United States
HybridFull Time
1+ YOESupports Alzheimer’s prevention studies including study visits, phlebotomy, cognitive testing, vascular ultrasound, specimen processing, recruitment, data entry; requires applicable training and clinical researcher credentialing.
2w
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Clinical Research Coordinator I - The School of Nursing - Alzheimer's Disease Prevention
Atlanta, Georgia, United States
OnsiteFull Time
3+ YOESupports Alzheimer’s prevention studies including study visits, phlebotomy, specimen processing, recruitment, data entry, and regulatory tasks; high school diploma/GED plus 3 years admin support or alternate degree/licensure options.
1mo
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Clinical Research Coordinator II - School of Medicine Orthopaedics
Flowery Branch, Georgia, United States
OnsiteFull Time
1+ YOEMust meet one of several education/experience pathways (HS/GED +5 yrs research, 2 yrs college +3 yrs, LPN +2 yrs, Bachelor's +1 yr, or Master's/MD/PhD). Responsibilities include managing study databases, consenting participants, specimen collection, and regulatory submissions; orthopaedics experience preferred.
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Clinical Research Manager (68740)
Atlanta, Georgia, United States
OnsiteFull Time
5+ YOERequires a bachelor's degree and 5+ years of clinical research experience, including study coordination or site management and direct supervision; knowledge of FDA, ICH-GCP, HIPAA, and IRB requirements.
FDA, ICH-GCP, HIPAA, IRB, SOPs, CAPAs
1mo
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Clin Research Coord I (ETS)| Temporary
Atlanta, Georgia, United States
OnsiteTemporary
1+ YOESupports clinical and preclinical research: regulatory submissions (IRB/IACUC), study coordination, data entry, patient recruitment, specimen collection (including phlebotomy). Requires HS/GED + admin experience or relevant college degree; preferred bachelor's or master's in life sciences and research experience.
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