Research Assistant

CARE

Research Assistant at Care Access facilitating decentralized clinical trials and engaging with patients. Responsible for study delivery and support under the guidance of the Principal Investigator.

Posted 7/10/2026full-timeRemote • 🇺🇸 United StatesJuniorMid-Level💰 $65,000 - $75,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research processes, including patient recruitment, regulatory documentation, and adherence to GCP and ALCOA-C standards. Proficient in utilizing clinical trial software and maintaining effective communication with stakeholders.

Highest-signal resume keywords

Clinical Research ExperienceGCP CompliancePatient Recruitment PlatformsMicrosoft Office ProficiencyRegulatory Document Preparation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ExperienceGCP ComplianceALCOA-C KnowledgePatient RecruitmentRegulatory Document PreparationResearch TerminologyMedical TerminologyTime ManagementAttention to DetailCritical Thinking

Soft Skills

Strong CommunicationCustomer Service AbilitiesProblem SolvingOrganization Skills

Tools & Technologies

Recruitment PlatformsIWRSEDCClinical Trial SoftwareMicrosoft WordMicrosoft OutlookMicrosoft TeamsMicrosoft Excel

Industry Keywords

Clinical Development ParadigmGovernment RegulationsPatient InteractionStudy ProtocolSite Teams

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Identify, recruit, educate, and pre-screen potential patients for a study
Analyze, understand, and be knowledgeable of the study protocol and the associated disease(s) in combination to educate patients and their families
Document all patient interaction appropriately and in accordance with GCP and ALCOA-C
Maintain up-to-date information across multiple study portals
Attend regularly scheduled meetings with PIs and their site teams
Negotiate contracts with potential facilities
Support the preparation of regulatory documents, obtain signatures from required personnel

Requirements

What you’ll need

A minimum of 2 years of relevant clinical research experience
Highly proficient at using a variety of technologies used for clinical research including recruitment platforms, IWRS, EDC, and other clinical trial software
Skillful with Microsoft Office applications (Word, Outlook, Teams, and Excel)
Strong communication customer service abilities
Proficient in research terminology and basic medical terminology
Understand the overall clinical development paradigm and excellent working knowledge of government regulations, GCP, and ALCOA-C
Strong organization and time management skills
High attention to detail
Critical thinker and problem solver
Proper home office set-up including a private space for participant communication and high-speed internet (at minimum: 100MB up and 15 MB down, 5 GHz router)
Spanish fluency is a bonus

Benefits

Comp & perks

Paid Time Off (PTO) and Company Paid Holidays
100% Employer paid medical, dental, and vision insurance plan options
Health Savings Account and Flexible Spending Accounts
Bi-weekly HSA employer contribution
Company paid Short-Term Disability and Long-Term Disability
401(k) Retirement Plan, with Company Match