Clinical Research Associate – U.S. Expert Network

Alcedis - a HUMA company

. Join Alcedis’s U.S.-based expert network of clinical research professionals .

Posted 9/18/2026part-timeRemote • New York • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core 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, 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

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Research AssociateOncology TrialsGCP RegulationsEPRO 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 Clinical Research

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Join Alcedis’s U.S.-based expert network of clinical research professionals
Support current and future clinical studies based on project needs and mutual availability
Conduct and support Site Initiation Visits, primarily virtually, in the U.S. and Canada
Perform on-site and remote monitoring activities
Work within the Clinical Operations team as a part-time project-based employee
Collaborate with colleagues across U.S. and European time zones, including Germany
Discuss study scope, timing, workload, and availability when a suitable project becomes available
Support projects primarily focused on Oncology and Alzheimer’s disease, 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 employee engagement for the duration of suitable projects
Flexible project-based work
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