Clinical Research Assistant: Impactful Trial Coordination

Alliance Clinical; Houston (TX); On-site; USD 42,000 - 65,000; Full time

Job summary

Alliance Clinical is seeking a Clinical Research Assistant to support clinical trials, coordinate study activities, and collect and document data. The role involves obtaining informed consent, managing investigational product accountability, processing samples, and maintaining regulatory documentation.

You will ensure protocol adherence, meet timelines, and deliver high-quality support to patients, investigators, and internal teams. Strong communication and organizational skills are essential.

Qualifications

• Bachelor’s degree in Biology or related field preferred or equivalent clinical experience.
• Proficiency in Microsoft Office and electronic data systems required.
• Strong knowledge of medical terminology.
• Ability to work independently with minimal supervision.
• Excellent verbal and written communication skills.
• Strong problem-solving abilities and adaptability in a dynamic environment.
• Outstanding customer service skills with internal teams and external stakeholders.

Responsibilities

• Coordinate protocol procedures and collect data per study protocol.
• Engage directly with study participants and obtain informed consent.
• Dispense and track study drug accountability as required.
• Perform protocol-specific procedures such as EKGs, vitals, and phlebotomy.
• Collect, process, and ship biological samples (blood, urine, tissue).
• Verify data accuracy and ensure timely documentation.
• Support IP storage and temperature monitoring.
• Interact with COVID-19-positive patients as needed.
• Assist with study startup documentation and timelines.
• Ensure compliance with regulatory standards and company policies.
• Maintain patient confidentiality and regulatory compliance.

Skills

Microsoft Office

Electronic data systems

Medical terminology

Communication skills

Independent work

Problem solving

Customer service

Education

Bachelor’s degree in Biology or related field

Tools

Electronic data capture systems

Job description

Alliance Clinical is seeking a Clinical Research Assistant to support clinical trials, coordinate study activities, and collect and document data. The role involves obtaining informed consent, managing investigational product accountability, processing samples, and maintaining regulatory documentation.

You will ensure protocol adherence, meet timelines, and deliver high-quality support to patients, investigators, and internal teams. Strong communication and organizational skills are essential.