Clinical Research Specialist: Data, Safety & Coordination

Houston Methodist; Houston (TX); Sur place; USD 55 000 - 85 000; Plein temps

Résumé du poste

Houston Methodist seeks a Clinical Research Specialist to support multiple projects under supervision of the Clinical Trial Manager. You will gather patient data per study protocol, ensure accurate data collection, and maintain documentation while prioritizing participant safety and regulatory compliance.

Responsibilities include data abstraction, coordinating with investigators and staff, and assisting with study reports.

Qualifications

• Bachelor's degree in a related field required.
• Health-Science related field preferred for enhanced eligibility.

Responsabilités

• Supports inter-professional team of investigators, nurses and coordinators.
• Performs data abstraction and recording in case report forms (CRFs).
• Requests and tracks informed consent for studies as needed.
• Coordinates data collection and documentation to ensure study integrity.

Connaissances

Data collection

Communication

Independent work

Patient safety

Time management

Interpersonal skills

Analytical thinking

Attention to detail

Formation

Bachelor's degree in related field

Bachelor's Degree in Health-Science related field preferred

Description du poste

Houston Methodist seeks a Clinical Research Specialist to support multiple projects under supervision of the Clinical Trial Manager. You will gather patient data per study protocol, ensure accurate data collection, and maintain documentation while prioritizing participant safety and regulatory compliance.

Responsibilities include data abstraction, coordinating with investigators and staff, and assisting with study reports.