In-House Clinical Research Associate

Alira Health; Framingham (MA); Hybrid; USD 50,000 - 70,000; Full time

Job summary

Alira Health is seeking an In-House Clinical Research Associate to support clinical sites from approval through close-out, with minimal travel and strong collaboration with field CRAs and PMs. This role emphasizes site regulatory management and data integrity in a fast-paced environment.

Ideal candidates hold a BA/BS and 1–2 years in clinical research, with excellent English communication, meticulous attention to detail, and the ability to multi-task across studies using MS Office tools.

Qualifications

• BS/BA from an undergraduate program or equivalent experience.
• 1-2 years of experience in clinical research.

Responsibilities

• Develops study documents and tools, including Informed Consent Form (ICF) templates for local and central IRBs.
• 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.
• Ensures all regulatory documents are collected and filed appropriately at both the site and in the Trial Master File (TMF); conducts routine file reviews.
• Analyzes site performance problems (protocol adherence) and identifies solutions; provides ongoing training for study sites.
• Maintains regular communication with study sites to ensure protocol/GCP compliance, assesses subject accrual rates, and responds to sponsor requests.
• Conducts remote review of data entered on electronic Case Report Forms (eCRFs).
• Works closely with field CRAs and data management to resolve queries on discrepant data.
• Assists with efforts to recruit investigative sites to participate in clinical studies.
• Complies with ICH GCP guidelines, FDA regulations, and company SOPs.
• Participates in internal, client/sponsor, scientific, and other meetings as required.
• Manages and resolves conflicting priorities to deliver on commitments.
• Performs additional duties as assigned.

Skills

Attention to detail

Organizational skills

Analytical thinking

Cross-functional collaboration

Communication skills

Problem-solving

English proficiency

Customer service orientation

Leadership potential

Education

BA/BS degree

Equivalent experience

Tools

MS Office

Excel

Word

Job description

In-House Clinical Research Associate page is loaded## In-House Clinical Research Associateremote type: Remotelocations: Framinghamtime type: Full timeposted on: Posted Todayjob requisition id: JR000624If so, please apply using the referral link emailed to you.Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.**Job Description Summary****Job Description**## ROLEThe In-house CRA is an important member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site approval through close-out. In-house CRAs work closely with field CRAs and Clinical Project Managers to ensure the integrity of the trial data without the need for frequent travel.## KEY RESPONSABILITIES* Develops study documents and tools, including Informed Consent Form (ICF) templates (for both local and central IRBs), site binder contents, etc.* 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* Ensures all regulatory documents are collected and filed appropriately at both the site and in the Trial Master File (TMF); conducts routine file reviews* Analyzes site performance problems (protocol adherence) and identifies solutions; provides ongoing training for study sites* Maintains regular communication with study sites to ensure protocol/GCP compliance, assesses subject accrual rates, and responds to sponsor requests* Conducts remote review of data entered on electronic Case Report Forms (eCRFs)* Works closely with field CRAs and data management to resolve queries on discrepant data* Assists with efforts to recruit investigative sites to participate in clinical studies* Complies with ICH GCP guidelines, FDA regulations, and company SOPs* Participates in internal, client/sponsor, scientific, and other meetings as required* Manages and resolves conflicting priorities to deliver on commitments* Performs additional duties as assigned## DESIRED QUALIFICATION & EXPERIENCE* BS/BA from an undergraduate program or equivalent experience* 1-2 years of experience in clinical research## TECHNICAL COMPETENCES & SOFT SKILLS* 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, yet less structured team environment* Ability to problem-solve unstructured or ambiguous challenges* 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.**Languages**English**Education**Bachelor of Arts (BA), Bachelor of Science (BS)**Contract Type**Regular**Salary Range**The final offer will be determined within the applicable location-specific range and will depend on the candidate's confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.$50,000 - $70,000 AnnuallyWith offices around the world, Alira Health provides a vibrant and creative environment with benefits that include professional development, global travel, flexible work programs and more. We welcome your passion and drive, talent and entrepreneurial spirit, sense of service and teamwork.We are an integrated team of over 800 scientists, strategists, economists, clinicians, and biostatisticians representing over 30 nationalities. This broad global perspective and cultural richness has a direct impact on providing innovative solutions for our clients that lead to higher standards of care and an improved patient experience.