Selected: ✨ Clinical Trial Assistant.
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🔥 2 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.
🔥 9 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%
🔥 14 hours ago
Remote Clinical Research Associate monitoring clinical trials for ICON’s sponsor partners. Ensuring protocol compliance, site performance, data integrity, and regulatory standards.
🔥 17 hours ago
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%
🔥 17 hours ago
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%
🔥 18 hours ago
Clinical Research Associate II monitoring clinical trials for ICON’s sponsor-dedicated research programs. Ensuring site compliance, data integrity, and patient safety across Galicia.
🕒 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
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
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
Clinical trial prescreening specialist reviewing EHR charts for a healthcare technology company. Screening patients for specialty-medicine trials and documenting eligibility findings.
🇵🇭 Philippines – Remote
💵 $7 / hour
⏳ Contract/Temporary
🟡 Mid-level
🟠 Senior
✨ Clinical Specialist
👻 Ghost score 0%
🕒 4 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
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
🕒 5 days ago
Clinical Operations Associate supporting NavDx HPV-driven cancer diagnostics for healthcare providers. Managing customer operations, testing workflows, surveillance adherence, and patient access across North and South Carolina.
🌲 North Carolina, South Carolina – Remote
💵 $65k - $75k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🏥 Clinical Operations
👻 Ghost score 0%
🕒 5 days ago
Clinical Operations Associate supporting NavDx cancer diagnostics for CareDx. Managing provider workflows, customer support, testing operations, and surveillance adherence across New York and New Jersey.
🏖️ New Jersey, New York – Remote
💵 $65k - $75k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🏥 Clinical Operations
👻 Ghost score 0%
🕒 5 days ago
Clinical Operations Associate supporting NavDx, CareDx’s blood-based cancer diagnostic test. Supporting healthcare providers, customer operations, testing workflows, and patient access across California.
🏄 California – Remote
💵 $65k - $75k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🏥 Clinical Operations
👻 Ghost score 0%
🕒 5 days ago
Clinical Research Associate monitoring Phase I–III clinical trials for AbbVie, an innovative medicines company. Ensuring site compliance, data quality, subject safety, and regulatory readiness.
🇨🇦 Canada – Remote
💵 CAD81k - CAD131k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🚫👨🎓 No degree required
👻 Ghost score 0%
🕒 5 days ago
Clinical Research Associate monitoring AbbVie’s Phase I–III clinical trials and investigative sites. Ensuring protocol compliance, data quality, subject safety, and regulatory readiness across Canada.
🇨🇦 Canada – Remote
💵 $81k - $131k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🚫👨🎓 No degree required
👻 Ghost score 0%
🕒 5 days ago
Clinical Research Associate monitoring investigator sites for Parexel’s clinical trials. Ensuring patient safety, GCP compliance, recruitment, and study quality across the Western US.
🇺🇸 United States – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 5 days ago
Clinical Research Associate conducting site monitoring for oncology and gastroenterology clinical trials. Supporting sponsors and sites through visits, compliance, data verification, and study documentation.
+250 More Clinical Trial Assistant Jobs Available!
We analyzed 10 job listings in the last year and found it takes about 17 days for employers to close a job opening.
We reviewed 13 job postings and found the top 10 skills employers are asking for most often are:
You need strong organizational skills, attention to detail, knowledge of clinical trial processes, proficiency in data entry and management, and familiarity with regulatory requirements. Good communication and teamwork skills are also important for remote collaboration.
Typically, a bachelor's degree in life sciences, nursing, or a related field is required. Relevant certifications in clinical research, such as ACRP or SOCRA, can be advantageous. Experience in clinical trials or research may also be beneficial.
Responsibilities include assisting with study documentation, managing trial databases, coordinating communications between stakeholders, monitoring study progress, and ensuring compliance with protocols and regulations. You'll also help prepare reports and maintain study files.
Benefits include flexible work hours, the opportunity to work from any location, reduced commuting costs, and improved work-life balance. Remote work allows for collaboration with diverse teams and access to a broader range of clinical projects.
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