Clinical Research Associate, U.S. Expert Network

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

📋 Description

• Become a part of Alcedis’s expert network of Clinical Research Associates based in the U.S.

• Assist with current and upcoming clinical studies as a member of the Clinical Operations team.

• Conduct and facilitate Site Initiation Visits, primarily through virtual means, across the U.S. and Canada.

• Execute both on-site and remote monitoring tasks.

• Discuss the scope, timing, workload, and availability for suitable projects as they arise.

• Work collaboratively with clinical research professionals and colleagues across U.S. and European time zones.

• Engage on a project basis as a part-time W-2 employee for the length of an assignment.

⛳️ 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 experience in oncology clinical trials.

• Practical experience with digital clinical trial solutions, including ePRO, eCOA, and eCRF systems.

• Ability to work independently and proactively, demonstrating a high level of ownership.

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

• Willingness to conduct and support Site Initiation Visits, mainly through virtual means, in the U.S. and Canada.

• Strong communication and organizational abilities.

• Proficient in written and spoken English.

• Must be based in the United States.

• Experience in Neurology and/or Alzheimer’s disease is highly advantageous.

• Background working within international or cross-border clinical research teams.

• Flexibility and ability to collaborate across U.S. and European time zones, including regular communication 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 throughout the duration of a project.

• Flexible work arrangements based on project needs.

• Opportunity to continue working with other clients outside the designated assignment, adhering to confidentiality and conflict-of-interest guidelines.

• Compensation for necessary project-specific qualification or pre-engagement activities involving actual work beyond the application and selection process.

• Access to select clinical trial projects.