16 clinical trials associate jobs at 11 companies in Washington, DC
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Clinical Trials Associate
Bethesda, Maryland, United States
$55k-$65k/yr OnsiteFull Time
Knowledge of ICH, GCP, and FDA regulations; clinical trials terminology; monitoring, regulatory documents, and trial master files. Requires strong communication, organization, time management, and multitasking skills.
HelpDesk, Electronic Data Capture (EDC)
2mo
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Senior Associate, Clinical Trials & Corporate Contracts
Baltimore, Maryland, United States
$76k-$86k/yr HybridFull Time
3+ YOEBachelor's degree and 3 years' related experience in contract development/negotiation or research/project management in a medical research environment; JD preferred; familiarity with clinical research, budgets, IP, and compliance.
3w
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Clinical Research Associate
Washington, District of Columbia, United States
$44k-$73k/yr OnsiteFull Time
5+ YOERequires bachelor's degree, 5+ years clinical trial coordinator experience, 3 years clinical patient-facing experience, neurology trial experience, regulatory maintenance, OnCore/CTMS data entry, and timely adverse event reporting.
OnCore/CTMS
1w
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Sr. Clinical Research Associate
Sparks or Arkansas or California or Colorado or Connecticut or Delaware or Florida or Idaho or Illinois or Indiana or Iowa or Wyoming or Kansas or Kentucky or Montana or Louisiana or Maine or Maryland or Massachusetts or Michigan or Minnesota or Mississippi or Missouri or Nebraska or Nevada or Ohio or Oklahoma or Oregon or Pennsylvania or Tennessee or Texas or Utah or Vermont or Virginia or Washington or Alabama or Arizona
RemoteFull Time
3+ YOEBachelor's degree in healthcare or science, 3 years of field-based CRA experience, clinical trial operations knowledge, and familiarity with GCP, FDA, ISO, HIPAA, and clinical research systems.
Veeva Vault CTMS, Veeva Vault CDMS, Veeva Vault, CTMS, CDMS, FDA CFR, ISO, HIPAA, IRB, EC, CROs, ALCOA
4w
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Clinical Scientist Associate Director – Early Development Inflammation
United States or Baltimore
$193k-$261k/yr RemoteFull Time
3+ YOEClinical development experience with protocol authorship, data review, and study execution; doctoral/master's/ bachelor experience levels accepted; strong communication and clinical trial compliance knowledge.
Spotfire
1w
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Clinical Research & Development Associate Principal Scientist
Gaithersburg, Maryland, United States
OnsiteFull Time
Bachelor's degree in a scientific field and considerable pharmaceutical drug development experience, including clinical trial interpretation. Knowledge of autoimmune diseases required; advanced degree and leadership experience preferred.
Good Clinical Practice (GCP), International Council for Harmonisation (ICH), Clinical Study Reports (CSRs), Common Technical Documents (CTDs), Investigational New Drugs (INDs)
1w
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Clinical Research & Development Associate Principal Scientist
Gaithersburg, Maryland, United States
OnsiteFull Time
Bachelor's degree in a scientific field, substantial pharmaceutical industry and drug development experience, clinical trial interpretation, autoimmune disease knowledge, and leadership of complex clinical projects.
GCP, ICH, CSRs, CTDs, INDs
4d
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MedTech Site Manager 1
Washington, District of Columbia, United States
$75k-$124k/yr OnsiteFull Time
2+ YOEBachelor’s degree in pharmacy, pharmaceutics, or a related scientific discipline; 2+ years of clinical trial experience; GCP and monitoring knowledge; EDC and clinical trial management systems experience.
Electronic Data Capture (EDC), Microsoft Office, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Endnote
1w
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Clinical Research & Development Associate Principal Scientist
Gaithersburg, Maryland, United States
OnsiteFull Time
Bachelor's degree in a scientific field and considerable pharmaceutical industry experience, including clinical trial interpretation, autoimmune disease knowledge, cross-functional leadership, GCP, ICH, regulatory, and project management expertise.
GCP, ICH, CSRs, CTDs, INDs
1mo
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Clinical Trial Recruitment Specialist
Baltimore, Maryland, United States
$20-$22/hr OnsiteFull Time
1+ YOEAssociate degree or equivalent, 1+ year relevant experience (call center experience required), knowledge of protocol eligibility and GCP, telehealth and participant screening skills.
1mo
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S & P Associate
Bethesda, Maryland, United States
$54k-$60k/yr HybridFull Time
BA/BS degree, strong attention to detail, excellent verbal/written communication, organizational and customer-service skills, proficiency in Microsoft Word/Excel/Outlook; MedDRA and clinical trial knowledge a plus.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft SharePoint
1d
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Associate Director, OBU Strategy
Gaithersburg, Maryland, United States
$193k-$290k/yr OnsiteFull Time
5+ YOEBachelor's degree and 5+ years in pharma, biopharma, or related fields; oncology development, clinical data, trial design, forecasting, market assessment, and strategic planning experience required. PhD preferred.
data tools, data platforms
6d
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Consulting Associate/Strategy & Medical Affairs (Life Sciences)
Boston or Chicago or New York City or Summit or Washington
$110k-$127k/yr HybridFull Time
PhD in a life sciences discipline preferred, up to 3 years of consulting or Medical Affairs experience, clinical trial and statistics knowledge, analytical ability, strong communication, and consulting methodology skills.
Microsoft Excel
1mo
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Breast Medical Oncology Physician
Washington, District of Columbia, United States
$20/yr OnsiteFull Time
Provide medical oncology care for breast cancer, develop and direct clinical trials, mentor faculty and trainees, academic appointment at associate professor level.
1w
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PRN Data Entry Specialist
Baltimore, Maryland, United States
$20-$22/hr OnsitePart Time
High school diploma or equivalent required; an associate degree or 60 college credit hours in a related field is preferred. Familiarity with clinical databases and Phase I trials is helpful.
Medidata Rave, REDCap, Electronic Data Capture (EDC)
1mo
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Pathology Medical Archives Coordinator (670288)
Baltimore, Maryland, United States
$17-$29/hr OnsiteFull Time
3+ YOEHigh school diploma required (Associate's in business preferred); minimum 3 years related experience; experience coordinating pathology records, release of information, subpoenas, shipping materials, and processing clinical trial requests.
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