Bilingual Clinical Operations Supervisor

Jcct; Houston, Northern (TX, KY); Hybrid; USD 70,000 - 90,000; Full time

Job summary

JCCT in Houston seeks a bilingual Site Supervisor to lead clinical operations, ensure regulatory and GCP compliance, and coordinate with CROs, sponsors, and investigators to deliver studies on time and within budget.

You will mentor CRCs, oversee Start-Up activities, and drive KPIs with the leadership team. Strong relationship skills, attention to detail, and a working knowledge of eClinical systems are required; travel to other sites may be needed.

Qualifications

• Minimum 4 years of experience in clinical research.
• Strong regulatory knowledge and ICH/GCP familiarity.
• Ability to lead a multifunctional team and manage timelines.
• Proficient in MS Office and eClinical systems.

Responsibilities

• Oversees clinical trial coordination and site leadership.
• Ensures protocol adherence, SOP compliance, and regulatory readiness.
• Develops relationships with investigators and CROs.
• Prepares reports and drives KPIs for leadership.
• Mentors CRCs and conducts performance reviews.

Skills

Relationship building

Team leadership

Regulatory compliance

GCP/FDA knowledge

Documentation

Attention to detail

MS Office

Travel readiness

Communication

Study coordination

Education

BS/BA Life Science

Tools

Medidata Rave

Inform

TrialKit

MS Office Suite

Job description

JCCT in Houston seeks a bilingual Site Supervisor to lead clinical operations, ensure regulatory and GCP compliance, and coordinate with CROs, sponsors, and investigators to deliver studies on time and within budget.

You will mentor CRCs, oversee Start-Up activities, and drive KPIs with the leadership team. Strong relationship skills, attention to detail, and a working knowledge of eClinical systems are required; travel to other sites may be needed.