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Clinical Research Coordinator III, Clinical Trials, Vaccine Research (Durational with Benefits)
Ontario, California, United States
$71k-$92k/yr OnsiteFull Time
2+ YOECollects and documents clinical trial data, prepares regulatory submissions, ensures compliance, and supports protocol implementation; requires clinical research experience and ability to interact with stakeholders.
1mo
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Clinical Trial Manager/Sr Clinical Trial Manager
San Diego, California, United States
$145k-$190k/yr HybridFull Time
5+ YOE5+ years (Clinical Trial Manager) or 7+ years (Senior) oncology clinical operations experience; preferred bachelor's in life sciences or allied health; experience with trial set-up, monitoring, close-out, vendor management, ICH-GCP and electronic data capture.
electronic data capture, IRT
3mo
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Senior Clinical Trial Manager (CTM)
United States
$168k-$188k/yr RemoteFull Time
5+ YOE2+ MgmtSenior CTM with 5+ years directing clinical trials in sponsor/CRO settings; strong GCP/ICH knowledge; regulatory submissions; TMF management; budget oversight.
TMF, GCP/ICH, Regulatory Submissions, Data Management, Biostatistics, Safety, Clinical Operations
1mo
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Trial Principal, Data & Analytics, Roivant Health
New York, New York, United States
$130k-$220k/yr OnsiteFull Time
Exceptional academic record; strong quantitative skills; experience with clinical trial data and evidence synthesis; ability to communicate with senior stakeholders.
R, Python, SAS, SQL
2mo
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Clinical Trial Biostatistician
Bethesda, Maryland, United States
OnsitePart Time
Master’s in Biostatistics or related field; experience producing CDISC SDTM/ADaM datasets; strong SAS programming; knowledge of FDA submission standards; GCP/ICH knowledge; strong communication.
SAS, CDISC, SDTM, ADaM, Define.XML, SDRG, ADRG
1d
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Clinical Trial Recruiter
Champaign, Illinois, United States
$37k-$51k/yr RemoteFull Time
Bachelor's preferred; prior sales, cold-calling, clinical research or patient recruitment experience preferred; knowledge of clinical protocols, medical terminology, EHRs, and data systems; strong communication and organizational skills.
Electronic Health Records
1d
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Clinical Trial Manager - Full Service
Morrisville, North Carolina, United States
OnsiteFull Time
Lead site management and clinical monitoring ensuring patient safety, protocol/GCP/regulatory compliance, data integrity; oversee CRAs/CeMs, risk mitigation, training, and trial deliverables.
Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards
3w
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Clinical Trial Research Assistant
Edwards, Colorado, United States
$23-$30/hr OnsiteFull Time
Supports clinical trial management including participant recruitment, data collection, study visit coordination, regulatory compliance, specimen processing; phlebotomy certification preferred; Spanish fluency preferred.
3w
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Clinical Trials Data Assistant
Chicago, Illinois, United States
$24-$28/hr OnsiteFull Time
2+ YOEHigh school diploma, 2 years data entry or similar experience, ability to manage and quality-check clinical trial data, familiarity with medical terminology, experience with oncology clinical trials and databases (SAS/Access) preferred.
Enterprise Applications, eIRB, Kronos, Mac OS X, Microsoft Exchange, SAS, Access
3w
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Clinical Data Analyst
Princeton, New Jersey, United States
OnsiteFull Time
Ensures accuracy and reliability of clinical trial data through validation, reconciliation, reporting, coordination with study teams, and quality improvement.
3mo
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Senior Clinical Data Manager
Rockville, Maryland, United States
$145k-$160k/yr OnsiteFull Time
6+ YOELead data management for clinical trials; ensure quality and timely data delivery; knowledge of CDISC, GCP; advanced degree with years of experience.
CDISC, CDASH, SDTM, GCP, DMP, DQC, eCRF, Trial Master File, Microsoft Office
5d
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Clinical Trial Specialist II
Nashville, Tennessee, United States
OnsiteFull Time
2+ YOECoordinate and manage Phase I-IV clinical research protocols, ensure GCP/ICH compliance, lead cross-functional study teams, maintain study documentation, and meet data deadlines.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft SharePoint, Microsoft OneNote
2mo
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Clinical Data Coder
Cincinnati, Ohio, United States
OnsiteFull Time
BSN and active RN required (or advanced clinical degree such as PharmD), experience coding medical/medication terms, familiarity with MedDRA and WHO Drug dictionaries preferred, clinical trials/pharmaceutical experience preferred.
MedDRA, WHO Drug Dictionary
1mo
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Senior Clinical Data Manager
Cambridge, Massachusetts, United States
$131k-$187k/yr OnsiteFull Time
7+ YOE7+ years in industry-sponsored clinical trials; lead data management; oversee CROs/vendors; Medidata Rave experience; CDISC/CDASH/SDTM/ADaM knowledge; oncology trial experience.
Medidata Rave, eCRF, CDASH, SDTM, ADaM
2mo
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PS Clinical Data Manager II
Salt Lake City, Utah, United States
OnsiteFull Time
2+ YOEBachelor’s degree in life sciences or related field; 2+ years clinical data management experience; knowledge of clinical trial regulatory basics; capable of high-quality data management for trials; immunization per CDC standards.
3mo
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Senior Clinical Trial Manager
Boston, Massachusetts, United States
$140k-$175k/yr HybridFull Time
5+ YOE5+ years in clinical operations for FDA-regulated devices or digital health; proven site management and IRB/submission experience; strong data management and cross-functional coordination.
2mo
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Clinical Trial Screening Coordinator
Tomball, Texas, United States
OnsiteFull Time
1+ YOECoordinate recruitment, pre-screening, data management; ensure eligibility; knowledge of GCP/FDA regulations; 3–4 yrs medical terminology; 1–2 yrs customer service; 1–2 yrs clinical research preferred.
CRIO, Electronic Data Capture, Microsoft Office
21h
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Clinical Trial Liaison - Cancer Center - Hybrid
Iowa City or Coralville
HybridFull Time
1+ YOEBachelor's degree (or equivalent),1-3 years research or clinical programming experience,knowledge of regulatory guidelines,experience with OnCore/REDCap/Labmatrix preferred,strong verbal/written communication and data management skills.
OnCore, REDCap, Labmatrix
2w
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Clinical Trial Research Coordinator I
Houston, Texas, United States
OnsiteFull Time
2+ YOECoordinate day-to-day research protocol activities, screen and enroll patients, collect and enter clinical data, maintain study and regulatory records, follow ICH/GCP guidelines.
Clinical Trial Management System, Electronic Data Capture (EDC)
3d
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Senior Clinical Data Manager
Durham, North Carolina, United States
$85k-$120k/yr RemoteFull Time
8+ YOE2+ MgmtUniversity/college degree,8 years combined DM experience including 2+ years sponsor management and 2+ years technical mentoring; knowledge of clinical trials, SOPs, GCP; strong communication and leadership skills.
Electronic Data Capture (EDC), SAS
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