Clinical Research Associate
Company: Selva Infosys LLC
- Location: Manchester, United States
- Seniority: Entry level
- Employment type: Full-time
- Posted: 14 days ago
- Offer language: English
Job description
Company Description Selva Infosys LLC operates at the intersection of medical practice compliance and automation-driven workflow optimization. The company provides a complete financial lifecycle framework designed to reduce operational friction and accelerate turnaround times. Its solutions help healthcare organizations streamline processes and improve accuracy in capturing financial value for patient care. Team members collaborate with healthcare stakeholders to support compliant, efficient, and technology-enabled clinical and administrative operations. Working at Selva Infosys LLC offers exposure to innovative healthcare automation and a mission focused on enhancing value across care delivery systems.
Role Description The Clinical Research Associate (CRA) is a full-time, on-site role based in Manchester, NJ. This role is responsible for monitoring clinical trial activities to ensure adherence to study protocols, regulatory requirements, and internal quality standards. Day-to-day responsibilities include reviewing source documents, maintaining accurate study records, and verifying data integrity across participating sites. The CRA will coordinate with investigators and site staff, support study start-up and close-out procedures, and assist in training site personnel on protocol-specific procedures. The role also involves preparing reports, tracking study progress, and collaborating with clinical operations and research teams to resolve issues and support timely trial completion.
Qualifications
- Experience with clinical trial protocols and the ability to interpret and apply protocol requirements to site activities.
- Hands-on experience as a Clinical Research Associate and familiarity with industry-standard CRA responsibilities.
- Knowledge of clinical trials processes, including patient enrollment, informed consent, and data collection procedures.
- Background in research methods and clinical operations, with skills in documentation, data review, and site coordination.
- Bachelor’s degree in life sciences, healthcare, or a related field; advanced degree or relevant certification (e.g., ACRP, SOCRA) is a plus.
- Understanding of Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements.
- Strong organizational, time management, and analytical skills, with attention to detail and accuracy.
- Effective written and verbal communication skills and the ability to collaborate with multidisciplinary clinical teams.
- Proficiency with common office and clinical research software tools; experience with electronic data capture (EDC) systems is beneficial.
