Clinical Research Coordinator I — Patient-Focused Trials

Alliance Clinical Network; Houston (TX); Sur place; USD 52 000 - 76 000; Plein temps

Résumé du poste

Alliance Clinical Network seeks a Clinical Research Coordinator I to support clinical trials by coordinating visits, collecting data, and ensuring protocol and regulatory compliance. The CRC will interact with participants, monitor health, and collaborate with the PI to uphold Good Clinical Practice (GCP) standards.

The role includes EKGs, data entry into EDC systems, and coordination with laboratories to ensure timely testing and reporting, while maintaining strict confidentiality and

Qualifications

• 2 years of phlebotomy and EKG procedures; CPT license preferred.
• Associate’s degree in healthcare or related field, or equivalent experience.
• Minimum 2 years of healthcare experience.
• Minimum 2 years of FDA regulations and Good Clinical Practice (GCP).
• Demonstrated analytical reasoning skills.
• Exceptional attention to detail and strong organizational skills.
• Excellent verbal and written communication abilities.
• Proven customer service skills with internal and external stakeholders.
• Ability to effectively manage multiple priorities in a fast-paced environment.

Responsabilités

• Coordinate study visits and data collection.
• Monitor participant health throughout the trial.
• Obtain informed consent and document patient history.
• Maintain regulatory files and ensure protocol compliance.
• Enter data into EDC and resolve data queries.
• Assist with monitoring visits and site readiness.

Connaissances

Phlebotomy

EKG

Analytical reasoning

Attention to detail

Organizational skills

Verbal communication

Written communication

Customer service

Multitasking

Formation

Associate’s degree in healthcare or related field

Description du poste

Alliance Clinical Network seeks a Clinical Research Coordinator I to support clinical trials by coordinating visits, collecting data, and ensuring protocol and regulatory compliance. The CRC will interact with participants, monitor health, and collaborate with the PI to uphold Good Clinical Practice (GCP) standards.

The role includes EKGs, data entry into EDC systems, and coordination with laboratories to ensure timely testing and reporting, while maintaining strict confidentiality and