Clinical Research Associate

Company Description I Verve Inc (i‑verve) is a technology services company that modernizes legacy platforms for regulated industries and integrates AI into existing systems. The organization supports clients in FinTech, banking, insurance, healthtech, and logistics, helping them meet complex compliance and regulatory deadlines such as PCI, ISO 20022/FedNow, FHIR R4, and Cures Act requirements. With headquarters in New Jersey and a delivery center in Ahmedabad, i-verve has a team of 80+ engineers and has operated since 2011. The company holds ISO 27001, ISO 9001, and SOC 2 Type II certifications and is a Microsoft AI Cloud Partner, providing a secure and high-quality environment for advanced technology projects. Team members collaborate on structured, assessment-led engagements that focus on measurable outcomes for clients.
Role Description The Clinical Research Associate (CRA) will support clinical studies that intersect healthcare, technology, and regulatory requirements for i-verve’s healthtech clients. In this remote, contract role, the CRA will oversee study site activities, ensure adherence to clinical protocols, and monitor data quality and regulatory compliance across assigned trials. Day-to-day responsibilities include coordinating clinical operations with site staff, reviewing source documents and case report forms, tracking patient recruitment and retention, and preparing monitoring visit reports and study documentation. The CRA will collaborate with cross-functional teams to align clinical trial execution with project timelines, risk management plans, and industry standards. The role also involves contributing to study start-up activities, assisting in training site personnel on protocol and procedures, and supporting audit readiness throughout the duration of the clinical trials.
Qualifications
Demonstrated experience in clinical research, including working as a Clinical Research Associate and supporting Clinical Trials.
Strong understanding of Clinical Operations and clinical study processes, including site management and data monitoring.
Ability to interpret and apply clinical Protocols and regulatory guidelines in research settings.
Proficiency in Research methodologies, documentation practices, and compliance with Good Clinical Practice (GCP).
Bachelor’s degree in life sciences, nursing, pharmacy, public health, or a related field; advanced degree is an asset.
Experience with healthtech, regulated environments, or technology-enabled clinical studies is beneficial.
Excellent organizational, communication, and stakeholder management skills in remote, cross-functional teams.
Comfort with digital tools for remote monitoring, electronic data capture (EDC), and collaboration platforms.

Work arrangement
No