Remote Clinical Trials Assistant: Study Ops & Documentation
Remote Jobs
- Remote job
Remote Jobs is seeking a Clinical Trials Assistant (CTA) to support Clinical Operations from a remote location. The role involves document control, study materials creation, and collaboration with sites to ensure regulatory compliance. The CTA will assist with study drug release, training materials, and investigator meetings, while maintaining training records and study contacts. Relevant experience in clinical research or regulatory affairs is preferred. #J-18808-Ljbffr Remote Jobs
- ...Supporting Clinical Operations in a remote full-time capacity, the Clinical Trials Assistant will manage essential documents for clinical trials, assist with study drug release, and participate in investigator meetings while ensuring compliance with regulatory guidelines...Remote workFull time
$15 per hour
Classification Title:OPS Clinical Trials Assistant Classification Minimum Requirements:High school diploma or equivalent Job Description: ~... ..., ensuring data integrity, completeness, and adherence to study protocol. Maintain and manage daily sample files in Excel,...SuggestedFull time- ...Description Job Description Clinical Trial Visit Flow Manager... ...assessments → completion of documentation → patient compensation and discharge... ...Verify that the correct study team has been notified. Prioritize... ...may include onsite and remote personnel: Onsite Visit...Remote workWork at officeImmediate start
- Southern New Hampshire University is seeking online adjunct faculty for the Undergraduate Quantitative Studies/Ops Management program. This remote role involves guiding students in asynchronous courses, providing feedback, and facilitating discussions. Courses include QSO...Remote job
- ...and sites. Ensure study conduct complies with... ...all phases of a clinical research study for... ...through the trial. Perform site management... .... Conduct remote/on-site monitoring... ...monitor regulatory documentation for start-up, maintenance... ...partners (ops, finance, regulatory...Remote workLocal area2 days per week3 days per week
$62.38k - $77.97k
...Clinical Study Specialist ICON is a global healthcare intelligence and... ...Contributes to review of study documents such as informed consent... ...investigator/site status for the trial, and supports with clinical... ...coverage Employee assistance programmes and wellbeing resources...Work experience placementWork at officeWork from home$120k - $145k
Senior Clinical Research Associate - Remote with 50% travel Full?Time | Clinical OperationsA... ..., high?impact clinical studies. This role is ideal for... ...data, and review study documentation to support timely and accurate... ...or high?acuity clinical trials Deep understanding of ICH...Remote workPermanent employmentFull timeInterim roleWork at office- ...improve the world's health. From clinical trials to regulatory, consulting,... ...patient safety and quality study execution in accordance with... ...site levelConduct onsite, remote/electronic monitoring as needed... ...all required reports, documentation, updates and tracking within...Remote workFull timeLocal area
- Regional Clinical Research Associate IIBIOTRONIK is one of... ...Associate II to our Clinical Studies team. Conduct on-site, remote, and centralized... ...through review of regulatory documents, medical records, reported... ...supporting medical device IDE trials is preferred.Strong...Remote workFull timeContract workWork at officeHome office
$93.9k - $153.3k
...for people with serious diseases. We are seeking a Clinical Study Specialist to join our Clinical Trial Management team. In this role, you will provide technical... ...assessments, and contributes to review of study documents (e.g., informed consent forms, case report forms)...Work experience placementWorldwide- ...manages global oncology trials and programs. The... ...for onsite and remote monitoring of phase l-lll oncology studies. The primary... ...study plansSource document verification:Verify... ...study issuesEnsure clinical data integrity and... ...is not accepting assistance from search firms...Remote workFull timeWork experience placementRelocationFlexible hoursNight shift
- Description Clinical Research Associate - Full... ...on-site or remotely) ensuring regulatory... ...adequately performed and documented for each subject/... ...of the clinical study data review and capture... ...the ISF with the Trial Master File (TMF).... ...appropriate, to assist employees or...Remote workContract workInterim roleLocal areaImmediate startFlexible hours
$120k - $135k
...science and robust clinical pipeline form the... ...overseeing clinical trial site management... ...support high-quality study execution, patient... ...Location: Fully Remote Salary Range: $120... ...and clinical trial documentation Proficiency with... .... If you require assistance or accommodation during...Remote workFull timeTemporary workWork at officeImmediate start$96.2k - $151.4k
...ensures compliance of study conduct with ICH/... ...all phases of a clinical research study,... ...all phases of the trial.Performs clinical... ...Plan and associated documents.Gains an in-depth... ...activities.Performs remote and on-site monitoring... ...unsolicited assistance from search firms...Remote workFull timeFor contractorsLocal areaFlexible hours2 days per week3 days per week- ...leader in robotic-assisted surgery and minimally... ...of PositionThe Clinical Research Associate... ...post-market clinical studies to ensure... ...managers, clinical trial assistants (CTAs)... ...of study-related documents (protocols, case report... ...Perform on-site and/or remote site qualification...Remote workInterim roleWork at officeLocal areaWorldwideFlexible hoursShift work
$100k - $125k
Senior Clinical Research Associate Valencia... ...device clinical studies from study start-... ...investigator site documentation, support audits and... ...with Clinical Trial Management, Data... ...required to support any remote/hybrid employee... ...leaveEmployee Assistance Program (24/7 mental...Remote workTemporary workInterim roleFlexible hours$135k - $145k
...We are advancing a clinical‐stage pipeline of... ...medium-sized clinical study or, with... ...overall clinical trial objectives. Additionally... ...SSF preferred with remote considered.Job Responsibilities... ...clinical sites. Assists with shipment and... ...of critical study documents such as informed...Remote workContract workWork at office$95k - $125k
...independent oversight of clinical centers to ensure... ...active clinical studies. The Clinical... ...Inspire clinical trials. Serve as a primary... ...questions. Perform remote and on-site monitoring... ...30% is required. Document site visits by... ...study team members. Assist clinical centers...Remote workWork experience placementLocal areaFlexible hours- ...Labcorp is seeking a Sr. Clinical Research Associate -... ...clinical validity studies in minimal residual disease... ...protections). Conduct remote monitoring activities... ...review of study documentation, data quality checks,... ...disability who needs assistance using our online tools...Remote workTemporary workCasual workInternshipWork at officeMonday to FridayFlexible hours
- ...Supporting the planning and implementation of clinical research, the full-time Clinical Research Assistant will maintain compliance with research protocols, assist with study treatments, and manage detailed documentation in a remote setting. Key responsibilities Supports...Remote workFull time
- ...Biosciences is seeking a Senior Clinical Research Associate to manage and monitor soft tissue ablation trials in the U.S. remote setup. The Sr. CRA will support study planning, site startup, patient... ...site monitoring, develop study documents, coordinate data reports,...Remote work
$120k - $135k
...actively seeking Clinical Research Associates... ...is fully remote but does require... ...essential role in assisting the process of creating... ...execution of the clinical trial plans and... ...I-IV Maintain documentation and data evaluations... ...monitoring activities meet study requirements...Remote work- ...Vitalief is seeking a Research Office Assistant to support a long-term NIH-funded study focused on women with Alcohol Use... ...in Newark, NJ, with some remote days as training progresses. The... ...coordinating schedules, maintaining documentation, and communicating across departments...Remote workWork at office
$105k - $140k
...Clinical Research Associate If you are an experienced... ...in the clinical trial setting. Our passionate... ...visits, including pre-study, initiation, monitoring... ...collection of regulatory documents; Performing data... ...where applicable; Assisting with data validation and...Remote workLocal areaWork from homeFlexible hours- ...intelligence and clinical research organisation... ...clinical trial delivery. This is a fully remote role based in The... ...Managing clinical studies in the Netherlands... ...visits Manage study documentation, regulatory submissions... ...Employee assistance programmes and wellbeing...Remote workWork from homeWorldwide
- ...Clinical Trial Rater – Borderline Personality Disorder (BPD)Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical... ...in accordance with the study protocol, GCP, and regulatory... ...DisorderAdminister, score, and document validated psychiatric rating...Remote workWorldwideFlexible hours
- ...phase I through phase IV clinical research studies and Real World... ...guidelines while working remotely. Key responsibilities... ...and timelines Assist with study start-up activities... ...essential regulatory documents Implement subject... ...1 year of clinical trial monitoring experience...Remote workFull time
- ...Associate Clinical Research SpecialistLocation... ..., 50% onsite, 50% remote) Duration: 16+... ...specialist is to perform study start-up and... ...specific essential document lists, managing and... ...as CTMS (Clinical Trial Management System)... ...conduct and closeout.Assisting in identifying...Remote workContract workWork experience placementImmediate start
- ...Clinical Project AssociateOrganOx is a commercial... ...(s) including Study Initiation, Enrollment... ...visits and remote monitoring visits... ...for the following:Assist in the review of protocols... ...review of study documents, including... ...completing other trials when necessary.Adhere...Remote work
$4,000 - $9,000 per month
...Clinical Research AssociateDotLab is transforming... ...DotLab clinical trials. This role will... ...focus on conducting remote site visits including monitoring of study data in accordance... ...of essential documents (e.g. study logs)... ...current and maintained; assist in audit readiness...Remote workWork at officeWorldwideFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Remote Clinical Trials Assistant: Study Ops & Documentation. Be the first to apply!
- clinical research assistant New York, NY
- on-site clinical research associate (traveling/remote) New York, NY
- clinical research associate cra New York, NY
- clinical research associate New York, NY
- clinical research administrator New York, NY
- senior clinical research associate New York, NY
- clinical trials assistant New York, NY
- software engineering manager remote New York, NY
- system engineer remote New York, NY
- remote technical project manager New York, NY


