Assistant Clinical Research Coordinator I

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

Summary:

The Assistant Clinical Research Coordinator I (ACRC I) supports the planning, coordination, and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and institutional policies while protecting participant safety and data integrity. Working closely with Principal Investigators (PIs), research staff, and study participants, the ACRC I assists with participant screening, data collection, and the coordination of study activities to ensure accuracy, efficiency, and high-quality research outcomes.

Essential Duties and Responsibilities:

• Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff.
• Recruit, screen, and enroll study participants in accordance with protocol requirements and ethical guidelines.
• Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams.
• Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards.
• Communicate with study participants to provide education, answer questions, and support adherence to study requirements.
• Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team.
• Support the preparation, maintenance, and submission of regulatory documents; assist with audits and inspections as needed.
• Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
• Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations.
• Scan, upload, file, and maintain organized study records and documentation.
• Apply critical thinking skills to support efficient study operations and problem resolution.
• Perform other duties as assigned.

Qualifications:

• High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred.
• Basic knowledge of clinical research principles, medical terminology, and healthcare environments.
• Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities.
• Ability to communicate clearly and professionally 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 principles, FDA regulations, and IATA guidelines preferred.
• Experience with participant recruitment, screening, and the informed consent process preferred.
• Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.

Certificates, Licenses, and Registrations:

• Medical Assistant (MA) certification preferred.
• Current CPR/BLS certification preferred.
• Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred.

ACN does not provide visa sponsorship for this role.

About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.