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 professionals located in the U.S.

• Assist in ongoing and upcoming clinical studies according to project requirements and mutual availability.

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

• Carry out both on-site and remote monitoring activities.

• Engage with the Clinical Operations team as a part-time project-based staff member.

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

• Discuss project scope, timelines, workloads, and availability when a relevant project arises.

• Primarily support projects targeting Oncology and Alzheimer’s disease, with expectations of involvement in additional therapeutic areas.

⛳️ Requirements

• Minimum of 3 years of practical experience as a Clinical Research Associate (CRA) or Clinical Monitor.

• Experience in GCP-compliant interventional clinical trials.

• Proven background in oncology clinical trials.

• Practical experience with digital tools for clinical trials, including ePRO, eCOA, and eCRF systems.

• Capacity to work autonomously and proactively, displaying a strong sense of ownership.

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

• Willingness to conduct and assist with Site Initiation Visits, primarily in a virtual format, in the U.S. and Canada.

• Excellent 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 in working with international or cross-border clinical research teams.

• Flexibility and capability to collaborate efficiently across U.S. and European time zones, particularly with colleagues based in Germany.

• Familiarity with U.S. and Canadian clinical trial regulations.

• Understanding of FDA regulations, HIPAA, and 21 CFR Part 11.

🏝️ Benefits

• Engagement as a part-time W-2 employee for the duration of relevant projects.

• Flexibility in project-based work arrangements.

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

• Compensation for necessary project-specific qualification or pre-engagement tasks that involve actual work beyond the application and selection phase.

• Access to select clinical trial projects.