Clinical Research Associate

Alira Health is a global team dedicated to innovation and collaboration. The Clinical Research Associate will conduct site monitoring responsibilities for clinical trials, ensuring protocol compliance and assisting with site-related issues.

Responsibilities

Performs qualification, initiation, interim, and close-out visits and ensures proper documentation of site visits

Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status

Facilitates adverse event reporting and ensures the reconciliation of SAE reports with source documentation and CRFs

Ensures integrity of CRF data through meticulous and thorough source document review and verification

Conducts investigational product accountability

Reviews regulatory binder for required documents

Works closely with in-house CRAs and data management to resolve queries on discrepant data

Proactively identifies site issues and develops problem-solving strategies for sites

Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests

Conducts audit preparation at study sites as needed

Works with other CRAs to maintain consistency and promote a collaborative team atmosphere

Manages and resolves conflicting priorities to deliver on commitments

Complies with ICH GCP guidelines, FDA regulations, and company SOPs

Participates in industry and client meetings

Performs additional duties as assigned

Company

Patient-centric healthcare consultancy and CRO for life sciences

Paris, Ile-de-France, FRA

https://www.alirahealth.com/

Founded in 1999

501-1000 employees

Qualifications

BS/BA from an undergraduate program or equivalent experience

2 years of clinical research experience

Ability to travel

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

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 country where you are applying

Patient-centric healthcare consultancy and CRO for life sciences.

Paris, Ile-de-France, FRA

https://www.alirahealth.com

Late Stage

Total Funding

$233M

Key Investors

Symbiotic Capital

Creadev

2024-12-17

Debt Financing· $100M

2023-01-09

Series Unknown· $58M

2022-01-13

Series Unknown· $40M

Leadership Team

Gabriele Brambilla

CEO

Annabel de Maria

Chief Patient Officer

Recent News

GlobeNewswire

Alira Health Joins PFMD Effort to Advance Patient-Centered Evidence Generation

2026-04-30

BioSpace

Alira Health and Autoimmune Neurology Alliance (AiNA) Launch AXIS Registry, Advancing Real-World and Patient-Centered Research in Autoimmune Neurology

2026-04-16

Global Medtech CDMO Market Grows to $96.5B in 2025 as Pharma-Medtech Convergence Emerges as a Defining Accelerator

2026-03-31

Required skills

Clinical Research, GCP Compliance, MS Office Suite, Site Monitoring, Adverse Event Reporting

Experience

2+ years