Clinical Research Assistant: Trials Data & Site Monitoring

BioTecNika Global; Austin (TX); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

Retirement savings plan

Paid time off

Job summary

DiaSorin in Austin, Texas, invites applications for a Clinical Research Assistant. This full-time, on-site role places you at the center of clinical study execution, site qualification, and IVDr data verification within a premier diagnostics environment.

You will support analytical method validation, monitor CRFs and EDCs, manage investigational site activities, ensure ICH/GCP compliance, and contribute to the drafting of study protocols and reports.

Qualifications

• Bachelor of Science in Biology, Molecular Biology, or related subject.
• DoE and data interpretation knowledge.
• Strong written and verbal communication.
• Experience in regulated GLP/GMP environments is a plus.

Responsibilities

• In-house & external study execution for analytical method validation and clinical trials.
• Monitor CRFs and EDC frameworks; identify and resolve discrepancies.
• Coordinate investigational site management and regulatory alignment.
• Support drafting of study protocols, DMRs, and BPRs.

Job description

DiaSorin in Austin, Texas, invites applications for a Clinical Research Assistant. This full-time, on-site role places you at the center of clinical study execution, site qualification, and IVDr data verification within a premier diagnostics environment.

You will support analytical method validation, monitor CRFs and EDCs, manage investigational site activities, ensure ICH/GCP compliance, and contribute to the drafting of study protocols and reports.