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Alcedis - a HUMA companyCore Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience as a Clinical Research Associate with a focus on Oncology and Alzheimer’s disease studies, proficient in GCP-regulated interventional clinical trials and digital solutions for clinical trials. Capable of conducting Site Initiation Visits and performing both on-site and remote monitoring activities while collaborating effectively across U.S. and European time zones.
Highest-signal resume keywords
Clinical Research Associate ExperienceOncology Clinical TrialsGCP-Regulated TrialsDigital Solutions for Clinical TrialsSite Initiation Visits
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Join Alcedis’s U.S.-based expert network of experienced Clinical Research Associates
- Support current and future clinical studies on a project basis within the Clinical Operations team
- Conduct and support Site Initiation Visits, primarily virtually, in the U.S. and Canada
- Perform on-site and remote monitoring activities
- Collaborate with colleagues across U.S. and European time zones, including Germany
- Discuss study scope, timing, workload, and availability when suitable projects arise
- Work as a part-time W-2 employee for the duration of a matched project
- Support primarily Oncology and Alzheimer’s disease studies, with additional therapeutic areas expected
Requirements
What you’ll need- 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
- 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
- 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
Benefits
Comp & perks- Part-time W-2 employment for the duration of a project when there is a mutual fit
- Flexibility to continue working with other clients outside the agreed assignment, subject to confidentiality and conflict-of-interest requirements
- Compensation for any required project-specific qualification or pre-engagement activities involving actual work beyond the application and selection process
- Access to selected clinical trial projects
- Paid part-time employee engagement for the duration of matched projects
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Research AssociateOncology TrialsGCP ComplianceEPRO SystemsECOA SystemsECRF SystemsOn-Site MonitoringRemote MonitoringFDA Regulations21 CFR Part 11
Soft Skills
Strong Communication SkillsOrganizational SkillsProactive OwnershipCollaboration SkillsFlexibility
Industry Keywords
Clinical TrialsNeurologyAlzheimer's DiseaseHIPAACross-Border Research