Job 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