Clinical Research Associate, U.S. Expert Network

This is a fully remote position, open to applicants in New York.

📋 Description

• Become a member of Alcedis’s U.S.-based network of skilled Clinical Research Associates.

• Provide support for ongoing and upcoming clinical studies on a project basis within the Clinical Operations team.

• Conduct and assist with Site Initiation Visits, mainly virtually, across the U.S. and Canada.

• Execute both on-site and remote monitoring activities.

• Collaborate with team members across U.S. and European time zones, including Germany.

• Engage in discussions regarding study scope, timelines, workload, and availability for suitable projects.

• Work as a part-time W-2 employee for the duration of a matched project.

• Primarily support studies focused on Oncology and Alzheimer’s disease, with additional therapeutic areas anticipated.

⛳️ Requirements

• A minimum of 3 years of practical experience as a Clinical Research Associate (CRA) / Clinical Monitor.

• Experience in GCP-regulated interventional clinical trials.

• Proven expertise in oncology clinical trials.

• Hands-on familiarity with digital solutions for clinical trials, such as ePRO, eCOA, and eCRF systems.

• Capability to work autonomously and proactively with a strong sense of ownership.

• Experience in both on-site monitoring and remote monitoring activities.

• Willingness to conduct and support Site Initiation Visits (mainly virtually) in the U.S. and Canada.

• Strong communication and organizational abilities.

• Excellent proficiency in written and spoken English.

• Must be based in the United States.

• Experience in Neurology and/or Alzheimer’s disease is a significant advantage.

• Background in international or cross-border clinical research teams.

• Ability and flexibility to collaborate efficiently across U.S. and European time zones, including regular interactions with colleagues in Germany.

• Knowledge of 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, adhering to confidentiality and conflict-of-interest regulations.

• 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 throughout the duration of matched projects.