Remote Clinical Research Associate – Site Monitoring

Syneos Health, Inc.; Louisiana; À distance; USD 90 000 - 120 000; Plein temps

Avantages offerts par ce poste

Company car or car allowance

Medical, Dental and Vision benefits

401k matching

Employee Stock Purchase Plan

Bonus eligibility

Paid time off

Résumé du poste

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to regionally support trials across the US, with focus on Louisiana-based sites.

The role includes monitoring, site qualification, initiation visits, and ongoing data verification, ensuring ICH-GCP compliance and sponsor expectations. You will work remotely with on-site visits as needed, travel up to 75% nationwide, and collaborate with cross-functional teams to drive study timelines, data integrity, and patient safety.

Qualifications

• 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 computer skills and be able to embrace new technologies.

Responsabilités

• 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 of subjects/patients; assesses safety and data integrity factors at sites.
• Assesses site processes, conducts Source Document Review, verifies CRF data accuracy, and drives query resolution to closure within timelines.

Connaissances

Communication skills

Interpersonal skills

Presentation skills

Travel up to 75%

Formation

Bachelor's degree or RN

Description du poste

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to regionally support trials across the US, with focus on Louisiana-based sites.

The role includes monitoring, site qualification, initiation visits, and ongoing data verification, ensuring ICH-GCP compliance and sponsor expectations. You will work remotely with on-site visits as needed, travel up to 75% nationwide, and collaborate with cross-functional teams to drive study timelines, data integrity, and patient safety.