Clinical Research Associate, U.S. Expert Network
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Job Description
Clinical Research Associate joining Alcedis, a Germany-based clinical research organization expanding in the United States. Supporting oncology and Alzheimer’s clinical trials through flexible, project-based monitoring assignments.
Responsibilities:
- 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
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