Clinical Research Associate – MedTech Trials & Monitoring

Regulatory Jobs; Lower Providence Township (PA); Sur place; USD 65 000 - 95 000; Plein temps

Résumé du poste

Globus Medical in Pennsylvania seeks a Clinical Research Associate to monitor study sites, ensure the rights and safety of participants, and maintain data integrity across trials in compliance with GCP and SOPs.

The CRA conducts site qualification, initiation, interim monitoring, and closeout activities, reviews source data, and collaborates with cross-functional teams to support study objectives and regulatory requirements. Willingness to travel up to 70% is required.

Qualifications

• Bachelor’s degree in science, healthcare, engineering, or related field with clinical research experience.
• Working knowledge of GCP and applicable regulations governing clinical studies.
• Ability to travel up to 70% of the time.

Responsabilités

• Conducts remote and on-site monitoring activities in compliance with SOPs and regulatory requirements.
• Reviews source documentation, verifies study data, and escalates issues including adverse events.
• Monitors site enrollment, data quality, and protocol compliance across multiple sites.
• Supports development and maintenance of study documents and monitoring plans.

Connaissances

Communication

Teamwork

Attention to detail

Formation

Bachelor's degree in science or healthcare

Outils

EDC

CTMS

MS Office

Description du poste

Globus Medical in Pennsylvania seeks a Clinical Research Associate to monitor study sites, ensure the rights and safety of participants, and maintain data integrity across trials in compliance with GCP and SOPs.

The CRA conducts site qualification, initiation, interim monitoring, and closeout activities, reviews source data, and collaborates with cross-functional teams to support study objectives and regulatory requirements. Willingness to travel up to 70% is required.