Remote Regional Clinical Research Associate

Syneos Health, Inc.; Texas; In loco; USD 80.000 - 110.000; Tempo pieno

Vantaggi offerti da questo lavoro

Company car or car allowance

Health benefits (medical, dental, and视

401k with company match

Employee stock purchase plan

Bonuses based on performance

Paid time off (PTO) and sick leave

Descrizione del lavoro

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate regionally aligned across the US. The CRA will perform site qualification, initiation, monitoring, and close-out visits, on-site or remotely, ensuring ICH-GCP compliance and proper documentation.

The role requires travel up to 75% and involves coordinating with site staff, keeping ISF/TMF up to date, and ensuring data integrity across multiple sites. Strong communication and regulatory knowledge are essential.

Competenze

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.

Mansioni

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
• Verifies the process of obtaining informed consent and protects confidentiality.
• Reviews Investigator Site File and trial master file to ensure accuracy and archiving requirements.

Conoscenze

Excellent communication

Interpersonal skills

Travel ability

Formazione

Bachelor’s degree or RN in a related field

Descrizione del lavoro

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate regionally aligned across the US. The CRA will perform site qualification, initiation, monitoring, and close-out visits, on-site or remotely, ensuring ICH-GCP compliance and proper documentation.

The role requires travel up to 75% and involves coordinating with site staff, keeping ISF/TMF up to date, and ensuring data integrity across multiple sites. Strong communication and regulatory knowledge are essential.