Clinical Research Associate (CRA) – U.S. Expert Network | Project Opportunities | Remote
About The Position
Alcedis is a clinical research organization headquartered in Germany with over 30 years of experience. We are expanding our presence in the United States and are building a network of experienced clinical research professionals to support our current and future clinical studies, primarily focusing on Oncology and Alzheimer’s disease. We are seeking experienced Clinical Research Associates (CRAs) to join our U.S.-based expert network. Opportunities may arise to support Alcedis as part-time W-2 employees on a project basis within our Clinical Operations team, offering flexibility to network members. Joining the expert network does not guarantee a project or minimum hours. Any project-specific qualification or pre-engagement activities beyond the application and selection process will be compensated if required.
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 solutions for clinical trials, such as ePRO, eCOA, and eCRF systems
- Ability to work independently and proactively with a high degree of ownership
- 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
Nice To Haves
- Experience in Neurology and/or Alzheimer’s disease is a strong plus
- Experience working in international or cross-border clinical research teams
- Ability and flexibility to collaborate effectively across U.S. and European time zones, including regular interaction with colleagues based in Germany
- Experience with U.S. and Canadian clinical trial requirements
- Familiarity with FDA regulations, HIPAA, and 21 CFR Part 11
Responsibilities
- Conduct on-site monitoring and remote monitoring activities.
- Conduct and support Site Initiation Visits (primarily virtually) in the U.S. and Canada.
Benefits
- Keep your flexibility
- Access to selected clinical trial projects
- Work as a paid part-time employee for the duration of the project
- Compensation for project-specific qualification or pre-engagement activities if required
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Education Level
No Education Listed
