Clinical Research Coordinator I: Start in Trials & Care

Socket.dev; Dallas (TX); On-site; USD 50,000 - 70,000; Full time

Job summary

Alliance Clinical Network seeks an Assistant Clinical Research Coordinator I to support planning, coordination, and execution of clinical studies in a healthcare setting. You will work with Principal Investigators, staff, and participants to ensure protocol compliance and data integrity.

The role involves participant screening, data collection, scheduling visits, and maintaining regulatory documents while adhering to SOPs and GCP guidelines.

Qualifications

• High school diploma or equivalent; associate’s degree preferred in health-related field.
• Basic knowledge of clinical research principles, medical terminology, and healthcare environments.
• Strong organizational, time management, and attention to detail with ability to manage multiple priorities.
• Clear and professional communication with diverse populations.
• Ability to work collaboratively in a fast-paced, team-oriented environment.
• Experience in clinical research or healthcare settings preferred.
• Knowledge of GCP, HIPAA, ALCOA, FDA regulations, and IATA guidelines preferred.
• Experience with participant recruitment, screening, and informed consent preferred.
• Proficiency with electronic data capture systems and trial management software preferred.

Responsibilities

• Assist in coordination and execution of clinical research protocols under PI and senior staff.
• Recruit, screen, and enroll study participants per protocol and ethics guidelines.
• Coordinate and schedule study visits, procedures, and follow-up with participants and clinical teams.
• Collect, record, and maintain accurate clinical research data and source documentation.
• Communicate with participants to educate, answer questions, and support adherence.
• Monitor progress and report adverse events, deviations, and issues to the team.
• Assist with regulatory documents, audits, and inspections as needed.
• Adhere to SOPs and Good Clinical Practice (GCP) guidelines.
• Draw, process, and ship laboratory specimens per regulations.
• Scan, upload, and maintain study records and documentation.
• Apply critical thinking to support efficient study operations.
• Perform other duties as assigned.

Skills

Clinical research knowledge

Data management

Communication

Teamwork

Attention to detail

Time management

Regulatory awareness

GCP knowledge

Microsoft Office

EDC systems

Education

Associate degree in health-related field

Bachelor’s degree preferred

Tools

Microsoft Office

Electronic Data Capture (EDC)

Clinical Trial Management Software

Job description

Alliance Clinical Network seeks an Assistant Clinical Research Coordinator I to support planning, coordination, and execution of clinical studies in a healthcare setting. You will work with Principal Investigators, staff, and participants to ensure protocol compliance and data integrity.

The role involves participant screening, data collection, scheduling visits, and maintaining regulatory documents while adhering to SOPs and GCP guidelines.