25 edc jobs at 16 companies in Maryland
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Director, Clinical Science
Cambridge or Gaithersburg or London or Mainz or New Jersey
$168k-$269k/yr OnsiteFull Time
10+ YOEAdvanced degree preferred, 10+ years clinical development experience, GCP expertise, oncology/immuno-oncology experience preferred, global trial leadership, EDC systems experience, strong cross-functional leadership.
EDC systems
2w
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Clinical Database Developer
Fort Detrick, Maryland, United States
OnsiteFull Time
5+ YOE5+ years clinical database development experience, Bachelor\u0002s degree in CS/IS/Health Informatics/Clinical Research, EDC and CDISC knowledge, CompTIA Security+ or ability to obtain, ability to get DoD security credentials.
EDC, CDISC, CDASH, SDTM, SAS
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Clinical Research Coordinator I (103351)
Rockville, Maryland, United States
$55k-$65k/yr OnsiteFull Time
Supports clinical trials from startup through closeout, performing participant visits, protocol adherence, regulatory document maintenance, EDC data entry, and vendor/IRB communication. Knowledge of GCP, IATA, and HIPAA expected.
EDC, EMR, Microsoft Excel, Microsoft Word, Microsoft Outlook
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Senior Clinical Research Associate - CNS - Southeast/MidAtlantic (Remote)
North Carolina or Florida or Maryland
$97k-$193k/yr RemoteFull Time
5+ YOE5+ years CRA experience, CNS experience required, 4-year degree or nursing degree, active residency in Southeast/Mid-Atlantic US, BLS/CPR not mentioned, proficiency with Microsoft Office, CTMS, and EDC systems.
Microsoft Office, CTMS, EDC Systems
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Lead Research Associate - Clinical Data Manager (REDCap)
Bethesda, Maryland, United States
$82k-$109k/yr HybridFull Time
2+ YOEMA/MS or BA/BS with extensive experience; 2+ years relevant clinical data management experience; experience with clinical research, EDC/EDC systems, REDCap or Medidata Rave; knowledge of CDISC, FDA, ICH, GCP; strong communication and technical skills.
REDCap, Medidata Rave, MS Office, Box
3w
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Clinical Research Coordinator (52088)
Bethesda or Herndon
$90k-$140k/yr OnsiteFull Time
Bachelor's in a related field, experience with EMR/CTMS/EDC, oncology clinical trial experience, knowledge of FDA/ICH-GCP, strong organizational and communication skills.
Electronic Medical Records (EMR), clinical trial management systems, electronic data capture platforms
2w
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Clinical Research Coordinator
Texas or Louisiana or Illinois or Maryland or Kansas or South Dakota or Hawaii
OnsiteFull Time
2+ YOEBachelor's in health-related field,2+ years coordinating clinical research,knowledge of trial processes,regulatory compliance,GCP,EDC/CTMS familiarity,strong organizational and communication skills.
electronic data capture (EDC), clinical trial management systems (CTMS)
1w
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Clinical Research and Quality Assurance Associate
Rockville, Maryland, United States
OnsiteContract
3+ YOEBachelor's in life sciences,3+ years clinical research or quality assurance in GxP environments,knowledge of ICH-GCP,FDA and GMP,strong organization and communication,proficiency with Microsoft Office and EDC/QMS.
Microsoft Office Suite, electronic data capture (EDC), quality management systems
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Lead Research Associate - Clinical Data Manager (REDCap)
Bethesda, Maryland, United States
$82k-$109k/yr HybridFull Time
2+ YOE2+ years relevant clinical data management experience (MA/MS with 2–4 years or BA/BS with 8+ years); experience with REDCap/EDC, CDISC, FDA/ICH/GCP knowledge, strong communication and technical skills.
REDCap, Medidata Rave, Microsoft Office, Box.com
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Medical Assistant - Clinical Research
Pikesville or Baltimore
OnsiteFull Time
Medical Assistant certification required; bachelor's degree OR 2 years college OR completion of a healthcare program OR relevant clinical trials experience. Phlebotomy training preferred. Proficiency with EMR, EDC, and CTMS; strong attention to detail and communication skills.
Electronic Medical Records (EMR), Electronic Data Capture (EDC), Clinical Trial Management System (CTMS)
3mo
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Sr Research Nurse (Oncology)
Baltimore, Maryland, United States
$75k-$132k/yr OnsiteFull Time
2+ YOEActive RN license in practicing state, Bachelor's in Nursing or related, minimum 2 years' specialty experience, knowledge of protocol development, regulatory compliance, GCP, data collection/EDC, patient/family education, and ability to manage multiple clinical trials.
Beacon, PRL website, Electronic data capture
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Clinical Research Nurse Coordinator
Baltimore, Maryland, United States
$100k-$113k/yr OnsiteFull Time
3+ YOEBSN and active Maryland RN license required, 3+ years clinical research/coordinator experience, ACLS (or obtain within 3 months), knowledge of GCP/ICH/FDA, EDC and Microsoft Office proficiency, ability to lift 50 lbs and stand for extended periods.
Microsoft Office Suite
3w
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Clinical Research Coordinator
Bethesda, Maryland, United States
$65k-$108k/yr OnsiteFull Time
1+ YOEBachelor’s in nursing/health sciences/public health/clinical research,1+ year supporting clinical trials,oncology trial experience preferred,knowledge of FDA/ICH-GCP,human subjects protection,EMR/CTMS/EDC experience,and ability to obtain public trust.
Electronic Medical Records (EMR), clinical trial management systems, electronic data capture platforms
3mo
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Clinical Systems Business Analyst (Jr & Mid) – Multiple Openings - Essex Management (Contingent Role)
Rockville, Maryland, United States
RemoteFull Time
1+ YOEBachelor’s degree in Health Informatics, Clinical Research, Public Health, IT, or related field; 1–3 years (Jr) or 3–6 years (Mid) in clinical IT/regulated environments; strong analytical, stakeholder engagement, and documentation skills; familiarity with EHR/EDC/CTMS; GxP/GCP experience preferred.
Jira, Confluence, Azure DevOps, SQL, Excel, Power BI, Tableau, Configuration management tools
1mo
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Director of Cyber Threat Intelligence (CTI)
Gaithersburg, Maryland, United States
$163k-$244k/yr HybridFull Time
10+ YOE5+ Mgmt10+ years in CTI or related domains, 5+ years leading technical CTI teams, Bachelor's in relevant field, deep MITRE ATT&CK/ICS expertise, detection-as-code experience (Sigma/KQL/SPL), TIP/SIEM/EDR tooling, OT/ICS familiarity, and relevant certifications (e.g., GCTI, GREM, GCIH, CISSP).
MITRE ATT&CK (Enterprise/ICS), Sigma, KQL, SPL, TIP, SIEM, EDR, MES, SCADA, PLC, CTMS, EDC, IRT, ELN, LIMS, HPC
1mo
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Senior Global Clinical Study Manager
Chicago or Dallas or Durham or Gilbert or Indianapolis or New York or Phoenix or Rockville or San Francisco or Tampa
$93k-$233k/yr RemoteFull Time
5+ YOE2+ MgmtBachelor's in life sciences,5+ years clinical research experience including 2+ years clinical study management; oncology and global trial experience; knowledge of ICH-GCP, regulatory requirements, financial management.
Microsoft Office, CTMS, EDC
1w
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Director of Cyber Threat Intelligence (CTI)
Gaithersburg, Maryland, United States
$163k-$244k/yr HybridFull Time
10+ YOE5+ Mgmt10+ years in CTI/detection/IR with 5+ years leading technical CTI teams; expertise with ATT&CK, attack path modeling, vulnerability intelligence, TIP/SIEM/EDR integrations, and executive reporting.
MITRE ATT&CK, TIP, SIEM, EDR, Sigma, KQL, SPL, MES, SCADA, PLC, CTMS, EDC, IRT, ELN, LIMS, HPC, case management
3mo
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Clinical Systems Business Analyst (Jr & Mid) – Multiple Openings - Essex Management (Contingent Role)
Rockville, Maryland, United States
RemoteFull Time
1+ YOEBachelor's in related field required; 1–3 years (Jr) or 3–6 years (Mid) clinical IT/informatics experience; skills in requirements elicitation, process analysis, clinical systems, and testing.
BPMN, UML, Microsoft Visio, EHR, EDC, CTMS, HL7, FHIR, CDISC, SNOMED, LOINC, OMOP, Jira, Confluence, Azure DevOps, SQL, Microsoft Excel, Power BI, Tableau
2mo
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Clinical Research Site Director
Baltimore, Maryland, United States
OnsiteFull Time
8+ YOE5+ Mgmt8+ years in clinical research; 5+ years managing multiple trials; experience managing teams; knowledge of FDA regulations and GCP.
EDC, IVRS
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Senior Global Clinical Study Manager
Durham or Phoenix or Gilbert or San Francisco or New York City or Indianapolis or Tampa or Rockville or Chicago or Dallas
$93k-$233k/yr OnsiteFull Time
5+ YOE2+ MgmtBachelor's in life sciences, 5+ years clinical research/monitoring (including 2 years study management), Phase III and oncology experience, ICH-GCP and FDA knowledge, global trial and financial management, stakeholder leadership.
Microsoft Office, CTMS, EDC
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