
Clinical Research Associate, U.S. Expert Network
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in New York.
• Become a part of Alcedis’s U.S.-based network of skilled Clinical Research Associates.
• Assist with current and upcoming clinical studies according to project requirements and mutual schedules.
• Carry out and assist with Site Initiation Visits, primarily conducted virtually, across the U.S. and Canada.
• Execute both on-site and remote clinical trial monitoring tasks.
• Collaborate with the Clinical Operations team and peers across U.S. and European time zones.
• Support projects that mainly focus on oncology and Alzheimer’s disease, with the expectation of additional therapeutic areas in the future.
• Serve as a part-time W-2 employee throughout the duration of the assigned project.
• A minimum of 3 years of practical experience as a Clinical Research Associate (CRA) / Clinical Monitor.
• Proficient experience in GCP-regulated interventional clinical trials.
• Proven experience in oncology clinical trials.
• Practical knowledge of digital clinical trial solutions, including ePRO, eCOA, and eCRF systems.
• Capacity to work independently and proactively with a strong sense of ownership.
• Experience conducting both on-site and remote monitoring activities.
• Willingness to perform and assist with Site Initiation Visits, primarily conducted virtually, within the U.S. and Canada.
• Strong communication and organizational abilities.
• Exceptional written and verbal English skills.
• Must be located in the United States.
• Experience in Neurology and/or Alzheimer’s disease is a significant advantage.
• Experience collaborating within international or cross-border clinical research teams.
• Flexibility and ability to work across U.S. and European time zones, including regular communication with colleagues based in Germany.
• Knowledge of U.S. and Canadian clinical trial requirements.
• Familiarity with FDA regulations, HIPAA, and 21 CFR Part 11.
• Part-time W-2 employee engagement during suitable projects.
• Flexible work arrangements based on project needs.
• Opportunity to continue working with other clients outside of the agreed assignment, subject to confidentiality and conflict-of-interest regulations.
• Compensation for project-specific qualification or pre-engagement activities that involve actual work beyond the application and selection process.
Mercor
Center for Social Dynamics
Karius
CTI Clinical Trial and Consulting Services
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