Senior Clinical Research Associate - Field-Based, 70% Travel

SRG; Houston (TX); Sur place; USD 90 000 - 120 000; Plein temps

Résumé du poste

SRG is seeking a Clinical Research Associate (CRA) to monitor clinical trial sites, ensure GCP compliance, and support study execution across multiple sites. This field-based role requires extensive site visits and travel, coordinating with cross-functional teams to maintain trial quality and timelines.

The role emphasizes interaction with investigative sites, regulatory compliance, and documentation, offering exposure to a large-scale, multi-region program and potential extension beyond the

Qualifications

• Minimum of 7 years of clinical monitoring experience in pharma, biotech, or CRO environments.
• Bachelor's degree in a scientific or healthcare-related field.
• Strong knowledge of clinical research operations, FDA regulations, ICH-GCP, and trial conduct.
• Excellent organizational, communication, problem-solving, and relationship-management skills.
• Experience with CTMS, eTMF, eCRF platforms, and Microsoft Office applications.
• Ability to manage multiple priorities with minimal supervision in a fast-paced environment.
• Willingness and ability to travel up to 70%, with no travel restrictions.

Responsabilités

• Conduct site monitoring visits including qualification, initiation, interim monitoring, and closeout activities.
• Ensure protocol compliance, data quality, and regulatory adherence.
• Serve as the primary contact for assigned investigative sites, communicating study updates and risks.
• Review and maintain Investigator Site Files and trial records.
• Prepare monitoring reports and escalate significant findings or site issues.
• Track site performance, recruitment progress, and study milestones.
• Support investigator training, study meetings, and other trial activities.
• Collaborate with internal teams, vendors, and site personnel to support study execution.

Connaissances

Organizational skills

Communication

Problem solving

Relationship management

Formation

Bachelor's degree in science/healthcare

Outils

CTMS

eTMF

eCRF

MS Office

Description du poste

SRG is seeking a Clinical Research Associate (CRA) to monitor clinical trial sites, ensure GCP compliance, and support study execution across multiple sites. This field-based role requires extensive site visits and travel, coordinating with cross-functional teams to maintain trial quality and timelines.

The role emphasizes interaction with investigative sites, regulatory compliance, and documentation, offering exposure to a large-scale, multi-region program and potential extension beyond the