Clinical Research Coordinator II

BioTalent; DeSoto (TX); On-site; USD 32,000 - 39,000; Full time

Job summary

BioTalent is seeking a Clinical Research Coordinator II in Desoto, TX to independently manage complex or high-enrolling clinical trials and ensure studies are conducted efficiently and in compliance with regulatory and protocol requirements.

The role involves coordinating with investigators, sponsors, and CRO partners, performing participant visits, and overseeing study performance metrics to drive quality and timely outcomes.

Qualifications

• Minimum 1 year of clinical research experience, preferably in industry-sponsored trials.
• Previous experience working on depression, psychedelic, or GLP-1 studies is highly preferred.
• Experience managing or supporting complex clinical studies.
• Strong organizational and communication skills.

Responsibilities

• Independently manage one or more complex or high-volume clinical trials.
• Conduct participant visits, eligibility assessments, and study procedures according to protocol.
• Oversee screening, enrollment progress, and study performance metrics.
• Serve as the primary point of contact for sponsors, monitors, and CROs.
• Support study start-up activities including regulatory preparation and site initiation visits.
• Maintain investigational product accountability and ensure proper documentation.
• Oversee data entry, resolve queries, and maintain inspection readiness.
• Train or support junior research staff assisting on assigned studies.

Skills

Strong organizational skills

Excellent communication skills

Clinical research experience

Job description

Clinical Research Coordinator II (CRC II)

Location: Desoto, TX

Compensation: $23-$28/Hourly

Hourly rate will be determined based on experience.

Overview

Our client is a growing clinical research site network focused on conducting industry-sponsored clinical trials to support the development of innovative treatments. They are seeking a Clinical Research Coordinator II to independently manage complex or high-enrolling clinical trials and ensure studies are conducted efficiently and in compliance with regulatory and protocol requirements.

This role is ideal for coordinators who have experience managing trials and want to take greater ownership of study execution while working closely with investigators, sponsors, and CRO partners.

Key Responsibilities

• Independently manage one or more complex or high-volume clinical trials.
• Conduct participant visits, eligibility assessments, and study procedures according to protocol.
• Oversee screening, enrollment progress, and study performance metrics.
• Serve as the primary point of contact for sponsors, monitors, and CROs.
• Support study start-up activities including regulatory preparation and site initiation visits.
• Maintain investigational product accountability and ensure proper documentation.
• Oversee data entry, resolve queries, and maintain inspection readiness.
• Train or support junior research staff assisting on assigned studies.

Qualifications

• Minimum 1 year of clinical research experience, preferably in industry-sponsored trials.
• Previous experience working on depression, psychedelic, or GLP-1 studies is highly preferred.
• Experience managing or supporting complex clinical studies.
• Strong organizational and communication skills.