Remote Clinical Research Associate – Global Site Monitor

Syneos Health, Inc.; Michigan; Sur place; USD 70 000 - 110 000; Plein temps

Avantages offerts par ce poste

Company car or car allowance

Health benefits (medical, dental, and视

401k match

Stock Purchase Plan

Bonuses based on performance

Flexible PTO

Résumé du poste

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) to be regionally aligned across the US. The role focuses on site qualification, initiation, monitoring, and close-out visits, either on-site or remote, ensuring ICH-GCP and protocol compliance.

You will verify informed consent, protect patient confidentiality, and assess factors impacting safety and data integrity throughout the study.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Must demonstrate good computer skills and be able to embrace new technologies.

Responsabilités

• Performs site qualification, initiation, monitoring, site management and close-out visits (on-site or remote) ensuring regulatory and protocol compliance.
• Verifies informed consent processes and protects confidentiality; assesses safety and data integrity factors.
• Reviews ISF, TMF reconciliation, and ensures archiving of essential documents per local guidelines.
• Maintains site processes per CMP/SMP; conducts source data review and data query resolution to closure.
• Supports subject recruitment, retention and data tracking; adapts to changing priorities to meet timelines.
• Acts as liaison with site personnel and participates in investigator meetings and sponsor meetings.

Connaissances

GCP/ICH knowledge

Strong communication

Computer skills

Willingness to travel

US work eligibility

Formation

Bachelor's degree or RN

Description du poste

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) to be regionally aligned across the US. The role focuses on site qualification, initiation, monitoring, and close-out visits, either on-site or remote, ensuring ICH-GCP and protocol compliance.

You will verify informed consent, protect patient confidentiality, and assess factors impacting safety and data integrity throughout the study.