Remote Clinical Research Associate – Global Site Monitoring

Syneos Health, Inc.; Florida; Remoto; USD 70.000 - 110.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health benefits

401(k) matching

Company car/allowance

Stock Purchase Plan

Flexible PTO

Descrizione del lavoro

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally aligned monitoring across the United States. You will perform site qualification, initiation, monitoring visits, and close-out activities, ensuring regulatory and protocol compliance in collaboration with the project team.

The role requires travel up to 75% and a strong knowledge of GCP/ICH guidelines, with excellent communication and data management skills to support site selection, data integrity, and

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.
• Must demonstrate good computer skills and be able to embrace new technologies.
• 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 (on-site or remotely) ensuring regulatory, ICH-GCP and/or GPP and protocol compliance.
• Verifies informed consent procedures and protects patient confidentiality.
• Reviews ISF and TMF, ensures archiving per guidelines.
• Manages IP inventory, reconciliation, and ensures proper labeling and handling per protocol.
• Documents activities and supports recruitment, retention and data tracking.

Conoscenze

GCP knowledge

Computer skills

Communication skills

Travel readiness

Formazione

Bachelor's degree or RN

Descrizione del lavoro

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally aligned monitoring across the United States. You will perform site qualification, initiation, monitoring visits, and close-out activities, ensuring regulatory and protocol compliance in collaboration with the project team.

The role requires travel up to 75% and a strong knowledge of GCP/ICH guidelines, with excellent communication and data management skills to support site selection, data integrity, and