Clinical Research Coordinator - 258761

Medix Staffing Solutions, Inc.; Euless (TX); On-site; USD 60,000 - 85,000; Full time

Benefits offered by this job

Job summary

Medix Staffing Solutions, Inc. is seeking a Clinical Research Coordinator in Euless, TX to manage day-to-day coordination of Phase II and III trials. You will oversee participant safety, data integrity, and protocol compliance in a fast-paced setting.

Responsibilities include patient recruitment, informed consent, data entry into EDC and CTMS, and collaboration with cross-functional teams to ensure trial milestones are met.

Qualifications

• Bachelor's degree in life sciences or related field, or equivalent experience.
• 2–5 years coordinating FDA-regulated clinical trials.
• Experience in Phase II/III sponsor-backed trials.

Responsibilities

• Coordinate Phase II and III trial activities from startup to closeout.
• Recruit, screen, enroll, and retain study participants with informed consent.
• Enter data into EDC and CTMS per ALCOA+ principles.
• Manage collection, processing, and storage of specimens; handle investigational products.

Skills

GCP knowledge

ICH guidelines

FDA standards

Data entry

Education

Bachelor's degree in life sciences

Tools

EDC systems

CTMS

eSource platforms

Job description

The Clinical Research Coordinator is responsible for managing day-to-day coordination and execution of clinical trials from startup through closeout. The position oversees participant safety, protocol compliance, data integrity, and cross-functional team collaboration. Operates within a fast-paced environment handling multiple concurrent active and non-active studies.

Responsibilities:

• Execute clinical trial protocols across Phase II and Phase III studies from start-up through study closeout.
• Recruit, screen, enroll, and manage study participants while leading informed consent processes and retention efforts.
• Collect, document, and enter study data accurately into electronic data capture (EDC) and CTMS systems following ALCOA+ principles.
• Manage biological specimen collection, processing, storage, and handling of investigational products.

Requirements:

• Bachelor's degree in life sciences, healthcare, or related field (or equivalent experience)
• 2 to 5 years of experience coordinating clinical research trials within an FDA-regulated site environment.
• Proven experience executing Phase II and Phase III commercial sponsor-backed trials.
• Strong ability to read, interpret, and execute complex clinical research protocols.
• Comprehensive understanding of Good Clinical Practice (GCP), ICH guidelines, and FDA regulatory standards.

Preferred Qualifications:

• Practical skills or certifications in phlebotomy, CPR, or Basic Life Support (BLS).
• Hands-on experience with electronic source (eSource) platforms and electronic data capture systems.
• Familiarity assisting with regulatory binder maintenance, patient recruitment, or registry management.