
In-House Clinical Research Associate
Alira Health
full-time
Posted on:
Location Type: Remote
Location: Massachusetts • United States
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Salary
💰 $85,000 - $100,000 per year
Tech Stack
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