Remote Clinical Research Associate for AI Document Training
Ethos
- Remote job
Ethos is seeking experienced clinical research associates to help train AI models on professional documents, spreadsheets, and slide decks. This fully remote role offers flexible 5–20 hours per week and a competitive hourly rate. Ideal candidates have 5+ years in clinical research, biomedical science, or regulatory affairs and can produce high-quality, regulation-compliant materials across study reports, protocols, and regulatory dossiers. #J-18808-Ljbffr Ethos
- ...Remote Based The Sr. CRA supports the day to day operations associated with the execution of clinical trials. He / she will monitor multiple... ...related study documents. The Sr. CRA is... ...responsible for site training, regulatory... ...aspects of clinical research and regulatory regulations...Remote workDocumentTrainingWork experience placementInterim role
$95k - $125k
OverviewThe Clinical Research Associate (CRA) supports clinical trial quality, compliance... ...oversight, and regulatory documentation. The CRA will also serve... ....Perform SDV, SDR, remote monitoring, data review, query... ...Support investigator/site training, investigator meetings,...Remote workDocumentTrainingWork at officeLocal area- AmsterdamClinical Services - Clinical Study Delivery - Monitoring... ...)Independently conduct and document onsite and remote activities, including site... ....Ensures site staff is trained in all aspects of the study... ...use artificial intelligence (AI) tools to support parts of...Remote workDocumentTrainingFull timeWork at officeLocal area
- ...coordinates all aspects of the clinical monitoring and site... ...process. Conducts remote or on-site visits to... ...and manages required documentation. Manages procedures and... ...+ years as a clinical research monitor). Valid driver... ...appropriate education, training and/or directly...Remote workDocumentTrainingWork at officeHome officeFlexible hoursNight shift
- Regional Clinical Research Associate IIBIOTRONIK is one of the leading manufacturers... ...team. Conduct on-site, remote, and centralized monitoring... ...through review of regulatory documents, medical records, reported... ...items, and study requirements.Train and mentor BIOTRONIK staff...Remote workDocumentTrainingFull timeContract workWork at officeHome office
- ...world's health. From clinical trials to regulatory,... ...locationsThe Clinical Research Associate is responsible for... ...Plan and associated Documents Gains an in-depth understanding... ...activities Performs remote and on-site... ...Complies with required training curriculum Completes...Remote workDocumentTrainingLocal area2 days per week3 days per week
- ...PSI is a leading Contract Research Organization with more than... ...Job Description As a Clinical Research Associate at PSI you will enjoy a... ...Review essential study documents and reconcile study Investigator... ...Conduct project-specific training of site investigators Support...Remote workDocumentTrainingContract workWork visa
$61.3k - $122.7k
...currently has an opportunity for a Clinical Research Associate. This role is based remote in the United States near a... ...and closeout visits. Provide training and support to investigators, study... ...requirements. Review source documents and verify clinical study data...Remote workDocumentTrainingWork experience placementWork at officeWorldwideShift work- ...Clinical Research Associate Opportunity When our values align, there's no limit to what we can achieve... ...you world class technology and training catered to your individual experience... ...and quality of Regulatory Documentation and perform site document verification...Remote workDocumentTrainingFlexible hours
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - South Central region At ICON Strategic Solutions... ...team and the sites Perform remote and on-site monitoring/co-... ...assess monitoring quality and train/mentor less experienced CRAs Promptly document monitoring activities and...Remote workDocumentTrainingFull timeInterim roleLocal areaWorldwide- ...of the PositionThe Senior Clinical Research Associate will play a vital role in supporting... ...and selection, training, scrutiny of potential patient... ...preparation of study-related documents and complete checklists,... ...performing on-site and/or remote site qualification visits,...Remote workDocumentTrainingInterim roleWork at officeLocal areaWorldwideFlexible hoursShift work
$95k - $125k
...independent oversight of clinical centers to ensure the... .... The Clinical Research Associate will ensure that clinical... ...by qualifying, training, monitoring, and overseeing... ...questions. Perform remote and on-site monitoring... ...30% is required. Document site visits by preparing...Remote workDocumentTrainingWork experience placementLocal areaFlexible hours- Job SummaryExperienced Clinical Research Associate (CRA) - join our growing team... ...Through our expedited PACE Training Program, you will receive... ...record and research source documentation verification against case... ...requirementsOn-site and virtual/remote monitoring activities with...Remote workDocumentTrainingContract workWork at officeWork from home
- ...Pharm Ds for the CRA role!The Clinical Research Associate position offers an... ...Cincinnati, OH.Medpace CRA Training Program (PACE)No prior research... ...and research source documentation verification against case... ...requirementsOn-site and virtual/remote monitoring activities with...Remote workDocumentTrainingContract workWork at officeWork from home
- ...Description Join Us as a Clinical Research Associate – Make an Impact at the... ...compliance with AZ Procedural Documents, international guidelines such... ...duration of the study. Trains, supports and advises... ...Performs monitoring visits (remote and onsite), as well as remote...Remote workDocumentTrainingWork at officeLocal area
- ...Team in Dallas, Texas!The Clinical Research Associate position offers an exciting... ...CoordinatorsMedpace CRA Training Program (PACE)No prior research... ...and research source documentation verification against case... ...requirementsOn-site and virtual/remote monitoring activities with...Remote workDocumentTrainingContract workWork experience placementWork at officeWork from home
$80k - $125k
.... Primary Role The Clinical Research Associate (CRA) is responsible for the... ...preparation of appropriate training materials and provide... ...maintenance of required essential documents and ensure these documents... ...goals Location Remote Salary Range $80-125...Remote workDocumentTrainingInterim role2 days per week1 day per week- ...Job Title: Clinical Research Associate Job Type: Contract Duration: 12 Months Field based... ...protocol and related study training to assigned sites and establish regular... ...copies/originals (as required) site documents are available for filing in the Trial...Remote workDocumentTrainingContract workLocal area
$105k - $118k
...team is currently seeking a Clinical Research Associate II with 1+ years of on-site... ...tools by careful source document Monitor data for missing or... ...management Assist with training of new employees, eg. co-monitoring... ...: $105 - $118K #LI - Remote Applications will be...Remote workDocumentTrainingWork at officeLocal areaNight shift$135k - $145k
.... We are advancing a clinical‐stage pipeline of differentiated... ...:The Sr. Clinical Research Associate (Sr. CRA) will... ...SSF preferred with remote considered.Job Responsibilities... ...of critical study documents such as informed... ...as needed for training and quality assurance...Remote workDocumentTrainingContract workWork at office- ...Job Description ROLE The Clinical Research Associate is an important member of the Alira... ...assist with study recruitment, site training, and other site-related issues. KEY... ...close-out visits and ensures proper documentation of site visits. Prepares consistently...Remote workDocumentTrainingPermanent employmentContract workInterim role
$95k - $120k
...partner is looking for a Clinical Research Associate – Wound Care... ...well as regulatory documentation, safety reporting, and... ...close-out visits, both remotely and onsite, ensuring... ...plans and training presentations, coordinate... ...works: We use an AI-powered matching process...Remote workDocumentTrainingInterim roleLocal areaFlexible hours- ...Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate... ...Hybrid SSF preferred with remote considered. Job Responsibilities... ...of critical study documents such as informed consent form... ...plan; monitors as needed for training and quality assurance (QA)...Remote workDocumentTrainingContract workWork at office
$91.79k - $137.68k
...City, CA (Hybrid) or Remote (USA)Clinical & Medical - Clinical... ...use of genomics and AI, we are driven to... ...SummaryThe Sr. Clinical Research Associate is responsible for... ...plan, conduct, and document on-site and remote monitoring... ...support site staff training and retraining on...Remote workDocumentTrainingFull timeInterim roleWork at officeLocal area- ...Sr. Clinical Research Associate Syneos Health® is a leading fully-integrated... ...technical and therapeutic area training; peer recognition and... ...visits (performed on-site or remotely) ensuring regulatory, ICH-... ...adequately performed and documented for each subject/patient...Remote workDocumentTrainingInterim roleLocal areaImmediate start
$90k - $130k
...partner is looking for a Clinical Research Associate – Wound Care based... ..., regulatory documentation, audit readiness, and... ...through mentoring, training, and consistent monitoring... ...environment, with remote work options and opportunities... ...: We use an AI-powered matching...Remote workDocumentTrainingContract workInterim roleLocal areaFlexible hours- ...support for BDPI clinical studies to enable... ...international clinical research regulations and... ...Conduct on-site or remote clinical site... ...essential clinical study documents for completion/... ...accuracy, conduct study training/presentations,... ...Clinical Research Associate team meetings, and...Remote workDocumentTrainingFull timeContract workInterim roleWork at office
- ...Senior Clinical Research Associate Location: Remote, Midwest or Western United States Employment Type: Contract... ...at least weekly • Provide training, guidance and ongoing support to... ...functional-area leads to develop study documents, including protocols, informed-...Remote workDocumentTrainingContract workWork at office
- ...0 AM - 5:00 PM Remote/Telecommuting Remote... ...Responsible for research activities, data... ...position works on clinical studies, which... ...Required Education: Associate's degree or equivalent... ...any degree major/training is required,... ...and creating source documents a plus. Preferred...Remote workDocumentTrainingFull timeTemporary workMonday to Friday
$50k - $70k
...member of the Alira Health Clinical team. In-house CRAs... ...Develops study documents and tools, including Informed... ...; provides ongoing training for study sites Maintains... ...requests Conducts remote review of data entered... ...in clinical research TECHNICAL COMPETENCES...Remote workDocumentTrainingPermanent employmentContract workLocal area
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