Selected: ✨ Clinical Research Assistant.
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Selected: 🆕 Date Added.
🔥 8 hours ago
Clinical trial feasibility specialist evaluating sites, risks, and trial readiness for ICON’s sponsor-dedicated clinical research programs. Preparing recommendations and guiding feasibility teams.
🔥 14 hours ago
Senior CRA monitoring oncology clinical trials for ICON, a global clinical research organization. Overseeing sites, compliance, data integrity, and trial execution across Mexico.
🔥 16 hours ago
Clinical Research Associate monitoring clinical sites and patient safety for BeOne, a company developing cancer medicines. Managing compliance, data quality, training, and study milestones.
🇺🇸 United States – Remote
💵 $92k - $122k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
👻 Ghost score 0%
🔥 16 hours ago
Senior Clinical Research Associate monitoring ophthalmology clinical trials for ICON’s sponsor-dedicated research programs. Supporting site performance, compliance, data integrity, and trial execution across the Northeast US.
🏖️ New Jersey, New York, +1 more states – Remote
💵 $110.5k - $138.2k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
👻 Ghost score 0%
🕒 Yesterday
Clinical Trial Assistant supporting clinical trial coordination, documentation, TMF, and vendor activities for a contract research organization. Remote role sourced by TransPerfect.
🗽 New York – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
✨ Clinical Trial Assistant
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 Yesterday
Clinical Trial Assistant supporting study coordination, documentation, and TMF activities for a global contract research organization. Managing trial sites, vendors, milestones, and regulatory records remotely.
🗽 New York – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
✨ Clinical Trial Assistant
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 Yesterday
Clinical study leader managing global immunology trials for AbbVie, a pharmaceutical company developing innovative medicines. Overseeing vendors, recruitment, compliance, study systems, risks, and cross-functional execution.
🕒 Yesterday
Senior Clinical Research Associate overseeing clinical trial sites for AbbVie, an innovative medicines company. Managing monitoring, compliance, recruitment, risk assessment and site partnerships.
🕒 3 days ago
Senior Clinical Research Associate advancing Novartis Phase I–IV clinical trials through site monitoring. Managing investigator relationships, compliance, patient safety, and reliable trial data across the U.S.
🌾 Iowa, Kansas, +5 more states – Remote
💵 $108.5k - $201.5k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 0%
🕒 3 days ago
Clinical Research Associate monitoring clinical trial sites for Syneos Health, a life sciences services company. Ensuring GCP compliance, data integrity, and site performance across Denmark and the Nordics.
🗣️🇩🇰 Danish Required
🕒 4 days ago
In-House Clinical Research Associate supporting document management, monitoring, and data review for Rho’s clinical trials. Collaborating with CRAs, sites, clients, vendors, and study teams.
🌐 Poland, United Kingdom, +4 more countries – Remote
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
👻 Ghost score 10%
🕒 4 days ago
Senior CRA overseeing site monitoring, compliance, and data quality for Worldwide Clinical Trials, a global CRO. Home-based East Coast role requiring 8–10 travel days monthly.
🚗 Michigan – Remote
💵 $97k - $193k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 0%
🕒 4 days ago
Clinical Research Associate monitoring investigative sites for Linical, a clinical research organization. Ensuring GCP compliance, participant safety, data integrity, and investigational product accountability.
🇺🇸 United States – Remote
💵 $95k - $135k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
👻 Ghost score 0%
🕒 4 days ago
Clinical Research Associate monitoring investigative sites for Linical, a clinical-trial CRO. Ensuring GCP compliance, participant safety, data integrity, and site performance.
🇺🇸 United States – Remote
💵 $95k - $120k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🚫👨🎓 No degree required
👻 Ghost score 0%
🕒 4 days ago
Clinical Registry Analyst abstracting and analyzing registry data for UW Health, Wisconsin’s #1 hospital. Ensuring accurate submissions through medical-record review and clinical-team collaboration.
🕒 4 days ago
Assistant CRA supporting remote site management, monitoring, documentation, and payments for pharmaceutical and biotech clinical trials. German-speaking role within a global clinical research team.
🗣️🇩🇪 German Required
🕒 4 days ago
Senior Clinical Research Associate monitoring pharmaceutical trials for Thermo Fisher Scientific. Managing investigator sites, compliance, data quality, and trial documentation across remote and on-site visits.
⛰️ Colorado – Remote
💵 $90k - $113k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 0%
🕒 5 days ago
Clinical Research Associate monitoring investigative sites and supporting clinical trial compliance for AbbVie. Advancing innovative medicines through recruitment, data integrity, safety, and site partnerships.
🕒 5 days ago
Senior Clinical Research Associate training junior CRAs and monitoring Phase II/III clinical trials. Supporting sites, investigators, audits, regulatory documents, and study tracking.
🗣️🇪🇸 Spanish Required
🕒 5 days ago
Clinical Research Associate conducting onsite monitoring and study startup activities for PSI, a contract research organization. Managing sites, reviewing clinical data, and supporting regulatory submissions.
🗣️🇪🇸 Spanish Required
+400 More Clinical Research Assistant Jobs Available!

We analyzed 5 job listings in the last year and found it takes about 40 days for employers to close a job opening.
We reviewed 6 job postings and found the top 10 skills employers are asking for most often are:
You need strong analytical skills, attention to detail, excellent communication abilities, and proficiency in data management software. Knowledge of clinical trial processes and regulations is also important.
Typically, a degree in life sciences, nursing, or a related field is required. Relevant certifications in clinical research can also enhance your qualifications. Experience in medical or research settings is beneficial.
Responsibilities include assisting with study protocols, collecting and analyzing data, maintaining study documentation, ensuring regulatory compliance, and collaborating with study teams and participants.
Benefits of working as a remote Clinical Research Assistant include flexible work arrangements, reduced commuting, the ability to manage your own schedule, and the opportunity to work with diverse teams across different locations.
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