Clinical Research Associate, U.S. Expert Network

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🔥 0 minutes ago

🗽 New York – Remote

🗽 New York – Remote

⏱ Part Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

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Alcedis - a HUMA company

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1992

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Alcedis - a HUMA company is a global contract research organization (CRO) that organizes and executes data-driven clinical studies and advances digital clinical research through proprietary technologies. It combines end-to-end clinical services — including project management, data management, monitoring, regulatory affairs, biostatistics, medical writing and pharmacovigilance — with software platforms (adaptive eCRFs, mobile apps, integrations) and AI/data-science capabilities to support biotech and pharmaceutical development from early-phase trials through regulatory approval and real-world evidence. Alcedis emphasizes technology-first, SaaS-style platforms to improve efficiency, data quality and patient-centric outcomes.

📋 Description

• Join Alcedis’s U.S.-based expert network of experienced Clinical Research Associates • Support current and future clinical studies within the Clinical Operations team as projects become available • Conduct and support Site Initiation Visits, primarily virtually, in the U.S. and Canada • Perform on-site and remote clinical trial monitoring activities • Collaborate with clinical research professionals and colleagues across U.S. and European time zones • Work on a part-time project basis for the duration of mutually agreed assignments • Discuss study scope, timing, workload, and availability when a suitable project becomes available

🎯 Requirements

• 3+ years of hands-on experience working as a Clinical Research Associate (CRA) / Clinical Monitor • Experience in GCP-regulated interventional clinical trials • Demonstrated experience in oncology clinical trials • Hands-on experience with digital clinical-trial solutions, such as ePRO, eCOA, and eCRF systems • Ability to work independently and proactively with a high degree of ownership • Experience with on-site monitoring and remote monitoring activities • Willingness to conduct and support Site Initiation Visits, primarily virtually, in the U.S. and Canada • Strong communication and organizational skills • Excellent written and spoken English • Based in the United States • Preferred: experience in Neurology and/or Alzheimer’s disease • Preferred: experience working in international or cross-border clinical research teams • Preferred: ability and flexibility to collaborate across U.S. and European time zones, including regular interaction with colleagues based in Germany • Preferred: experience with U.S. and Canadian clinical trial requirements • Preferred: familiarity with FDA regulations, HIPAA, and 21 CFR Part 11

🏖️ Benefits

• Part-time W-2 employment on a project basis for the duration of a project • Flexible participation based on project needs and mutual availability • Ability to continue working with other clients outside the agreed assignment, subject to confidentiality and conflict-of-interest requirements • Compensation for required project-specific qualification or pre-engagement activities involving actual work beyond the application and selection process • Access to selected clinical trial projects through the expert network