Senior Site Identification Analyst (Contractor) (Clinical Trials)

Location: United States of America

Company

hirify.global supports biotech, medtech, and specialty pharmaceutical companies in developing medicines, medical devices, and diagnostics through clinical research services.

What you will do

• Build and maintain internal and external relationships to gather business intelligence for financial and operational activities.
• Oversee site outreach for post-award site identification, standalone paid feasibility, and pre-award blinded outreach activities.
• Track site identification activities in CTMS, manage study timelines and project requirements, and coordinate with customers and vendors.
• Distribute, track, and review site request questionnaires for completeness, site capability, and availability.
• Update investigator and site databases, identify potential sites using performance metrics and medical informatics data, and review entries for duplicates.
• Review and tier sites for contact and support proposals, budgets, business development activities, and client meetings.

Requirements

• Undergraduate degree or international equivalent, preferably in science or a related field.
• 4+ years of experience in data management, clinical operations, or study start-up within the pharmaceutical, biotech, or medical device industry.
• 4+ years of experience supporting clinical trials, managing site partnerships, identifying or selecting sites, or working in the pharmaceutical industry.
• Strong analytical and problem-solving skills.
• Working knowledge of clinical database applications, including EDC and CTMS.
• Must be based in the United States of America.

Culture & Benefits

• Full-time 1099 contractor opportunity.
• Flexibility and balance to support professional and personal needs.
• Opportunities to develop skills and grow within clinical research operations.
• Equal opportunity employment compliant with applicable federal guidelines.