In House Clinical Research Associate

Alira Health

In-house Clinical Research Associate managing clinical sites for Alira Health. Supporting trials from approval through close-out with a focus on compliance and data integrity.

Posted 5/20/2026full-timeRemote • Massachusetts • 🇺🇸 United StatesJuniorMid-Level💰 $55,000 - $70,000 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage and support clinical sites from site approval through close-out
Develop study documents and tools, including Informed Consent Form (ICF) templates
Support sites in obtaining IRB approval and developing submission materials
Respond to sites’ regulatory board requests for protocol and ICF clarification
Ensure all required site regulatory documents are in place prior to investigational product shipment
Conduct routine file reviews and analyze site performance problems
Maintain regular communication with study sites to ensure compliance
Conduct remote review of data entered on electronic Case Report Forms (eCRFs)
Assist with efforts to recruit investigative sites to participate in clinical studies
Comply with ICH GCP guidelines and FDA regulations
Participate in internal, client/sponsor, scientific, and other meetings as required
Manage and resolve conflicting priorities to deliver on commitments

Requirements

What you’ll need

BS/BA from an undergraduate program or equivalent experience
1-2 years of experience in clinical research
Proven ability to be careful, thorough, and detail-oriented
Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment
Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills
Self-starter who thrives in a collaborative environment
Strong command of English, both written and verbal
Excellent communication and interpersonal skills with customer service orientation
Proficient with MS Office Suite, particularly Word and Excel
Permanent authorization to work in the U.S.

Benefits

Comp & perks

Professional development
Global travel
Flexible work programs

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical researchregulatory compliancedata analysisprotocol developmentInformed Consent Form (ICF) developmenteCRF reviewsite performance analysisIRB approval processstudy document developmentinvestigational product management

Soft Skills

detail-orientedorganizational skillsmulti-taskinganalytical skillsnegotiation skillsmeeting managementleadership skillscollaborativecommunication skillsinterpersonal skills