Alira Health

In-House Clinical Research Associate

Alira Health

full-time

Posted on:

Location Type: Remote

Location: MassachusettsUnited States

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Salary

💰 $85,000 - $100,000 per year

About the role

  • Manage and support clinical sites from site approval through close-out
  • Develops study documents and tools, including Informed Consent Form (ICF) templates
  • Supports sites in obtaining IRB approval, developing submission materials, and creating site-specific ICFs
  • Responds to sites’ regulatory board requests for protocol and ICF clarification as needed
  • Ensures all required site regulatory documents and approvals are in place prior to investigational product shipment
  • Analyzes site performance problems (protocol adherence) and identifies solutions
  • Maintains regular communication with study sites to ensure protocol/GCP compliance
  • Conducts remote review of data entered on electronic Case Report Forms (eCRFs)
  • Assists with efforts to recruit investigative sites to participate in clinical studies
  • Complies with ICH GCP guidelines, FDA regulations, and company SOPs

Requirements

  • 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 skills
  • Self-starter who thrives in a collaborative, yet less structured team 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
  • Professional development
  • Global travel
  • Flexible work programs
Applicant Tracking System Keywords

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

Hard Skills & Tools
clinical researchprotocol adherenceInformed Consent Form (ICF) developmentregulatory document managementdata analysiseCRF reviewIRB approval processGCP complianceFDA regulationsICH GCP guidelines
Soft Skills
detail-orientedorganizational skillsmulti-taskinganalytical skillsself-startercollaborativecommunication skillsinterpersonal skillscustomer service orientationthoroughness