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🔥 8 hours ago
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Clinical Research Associate II at Thermo Fisher Scientific managing clinical monitoring and site management processes. Ensures compliance with protocols and develops collaborative relationships with investigational sites.
🔥 13 hours ago
Clinical Research Associate I/II managing trial conduct and site relationships in Chengdu, China. Ensuring compliance with study protocol and assisting in site management tasks.
🕒 Yesterday
Clinical Trials Associate providing administrative and project tracking support for clinical trial teams. Responsibilities include maintaining documentation, coordinating system access, and supporting project related information.
🕒 Yesterday
Clinical Trial Associate at ICON overseeing and supporting clinical trials execution with compliance and efficiency focus. Collaborating with teams to ensure high standards and address trial challenges.
🕒 6 days ago
Senior Clinical Research Associate overseeing clinical trials ensuring compliance with protocols and regulatory standards for ICON. Collaborating with teams and site personnel to maintain data integrity and participant safety.
🕒 Yesterday
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Clinical Trial Assistant facilitating clinical trial activities for Iovance Biotherapeutics. Providing administrative support and managing study materials within clinical operations.
🕒 2 days ago
Clinical Research Associate monitoring clinical studies and ensuring compliance. Engaging with investigative sites and managing study setup activities.
🇹🇷 Turkey – Remote
💰 $75M Private Equity Round on 2015-12
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🗣️🇹🇷 Turkish Required
🕒 2 days ago
Clinical Research Associate conducting clinical trial monitoring at ICON. Ensuring compliance and maintaining strong stakeholder relationships in clinical programs for better patient outcomes.
🕒 2 days ago
Clinical Research Associate II managing clinical trials for ICON, a global healthcare intelligence organization. Collaborating on trial monitoring and data management with investigators and site staff.
🕒 2 days ago
Clinical Research Associate designing and analyzing clinical trials at ICON. Monitoring obesity and cardio studies and ensuring high-quality clinical data throughout the trial process.
🕒 2 days ago
CRA I at ICON delivering clinical trial monitoring work and coordinating clinical trial operations in Buenos Aires. Ensuring compliance with procedures, protocols, and regulatory requirements while building relationships with stakeholders.
🕒 2 days ago
201 - 500
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
Clinical Research Associate monitoring oncology trials for TRIO. Performing site visits, data verification, and ensuring compliance with regulations in a remote role.
🗣️🇫🇷 French Required
🕒 3 days ago
Clinical Research Associate II or Sr responsible for monitoring clinical trials and building site relationships. Collaborating with teams to ensure study compliance and integrity within a remote setting.
🗣️🇧🇷🇵🇹 Portuguese Required
🕒 4 days ago
Clinical Research Associate role at ICON focused on clinical trial monitoring and compliance. Collaborating with stakeholders to ensure study efficiency and patient safety in Italy.
🕒 4 days ago
Clinical Research Associate managing clinical trial monitoring. Working collaboratively to ensure high-quality outcomes across clinical programmes at ICON.
🕒 6 days ago
Job not on LinkedIn
Clinical Research Associate managing clinical trials at Emerald Clinical, a leader in clinical research. Performing monitoring activities and site management with a focus on quality and compliance.
🕒 6 days ago
Clinical Research Associate at ICON responsible for high-quality clinical trial monitoring and compliance. Collaborating with stakeholders to ensure patient safety and adherence to protocols in clinical research.
🕒 6 days ago
Clinical Research Associate at ICON responsible for high-quality clinical trial monitoring and compliance. Collaborating with stakeholders to ensure patient safety and adherence to protocols in clinical research.
+103 More Medical Research Assistant Jobs Available!
Strong analytical and research skills, attention to detail, proficiency in data analysis software, and excellent communication skills. A good understanding of medical terminology and research methodologies is also important.
A degree in life sciences, health sciences, or a related field is typically required. Relevant certifications in research methods or data analysis, along with experience in clinical settings, can be advantageous.
Responsibilities include conducting literature reviews, collecting and analyzing data, assisting in writing research proposals and reports, maintaining research databases, and ensuring compliance with ethical standards and regulations.
Benefits include flexible work hours, the ability to work from various locations, reduced commuting expenses, and improved work-life balance. Remote positions also often provide exposure to diverse research projects and collaboration with professionals across the globe.
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