Clinical Trials Site Lead — Operations & Team Growth

Iterative Scopes; Tyler (TX); On-site; USD 90,000 - 130,000; Full time

Job summary

Iterative Health is seeking a Research Site Manager to oversee day-to-day operations across clinical research sites, lead staff, and drive enrollment performance. You will implement standardized workflows, manage budgets, and ensure high-quality, compliant study execution.

The role requires clinical research leadership experience, strong communication, and the ability to travel across facility sites. You will collaborate with CROs, sponsors, and investigators to optimize site health and study

Qualifications

• Bachelor’s degree in a science discipline or equivalent experience.
• Minimum 3 years as a senior Clinical Research Coordinator; some management experience preferred.
• Strong written and verbal communication skills.
• Read, interpret, and apply clinic policies and research protocols.
• Proficiency with standard office software; EMR/CTMS experience preferred.

Responsibilities

• Manage day-to-day activities across research site(s) including staff management and operations.
• Create and implement standardized clinic workflows to drive operational excellence.
• Attend site selection visits and site initiation visits (SIVs).
• Oversee inventory and ensure adequate stock levels.
• Manage site-level purchasing and expenses to meet profitability goals.
• Serve as backup CRC as needed to balance workloads.
• Oversee employee lifecycle for site staff (hiring, onboarding, reviews, offboarding).
• Ensure timely completion of tasks in EMR and CTMS by CRCs and RAs.

Skills

Staff management

Enrollment growth

Operational planning

EMR/CTMS proficiency

Team leadership

Problem solving

Communication

Travel readiness

Education

Bachelor’s degree in science

Tools

EMR

CTMS

Salesforce

Job description

Iterative Health is seeking a Research Site Manager to oversee day-to-day operations across clinical research sites, lead staff, and drive enrollment performance. You will implement standardized workflows, manage budgets, and ensure high-quality, compliant study execution.

The role requires clinical research leadership experience, strong communication, and the ability to travel across facility sites. You will collaborate with CROs, sponsors, and investigators to optimize site health and study