Clinical Research Associate, U.S. Expert Network

🔥 1 minute ago

🗽 New York – Remote

🗽 New York – Remote

⏱ Part Time

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 12%

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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 on a project basis within the Clinical Operations team • Conduct and support Site Initiation Visits, primarily virtually, in the U.S. and Canada • Perform on-site and remote monitoring activities • Collaborate with colleagues across U.S. and European time zones, including Germany • Discuss study scope, timing, workload, and availability when suitable projects arise • Work as a part-time W-2 employee for the duration of a matched project • Support primarily Oncology and Alzheimer’s disease studies, with additional therapeutic areas expected

🎯 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 solutions for clinical trials, 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 • Experience in Neurology and/or Alzheimer’s disease is a strong plus • Experience working in international or cross-border clinical research teams • Ability and flexibility to collaborate effectively across U.S. and European time zones, including regular interaction with colleagues based in Germany • Experience with U.S. and Canadian clinical trial requirements • Familiarity with FDA regulations, HIPAA, and 21 CFR Part 11

🏖️ Benefits

• Part-time W-2 employment for the duration of a project when there is a mutual fit • Flexibility to continue working with other clients outside the agreed assignment, subject to confidentiality and conflict-of-interest requirements • Compensation for any required project-specific qualification or pre-engagement activities involving actual work beyond the application and selection process • Access to selected clinical trial projects • Paid part-time employee engagement for the duration of matched projects