Remote & On-Site Clinical Research Associate (CRA II)

Syneos Health, Inc.; South Dakota; Hybrid; USD 75.000 - 105.000; Vollzeit

Benefits dieser Stelle

Company car/allowance

Health benefits

401k matching

Employee stock purchase plan

Bonus eligibility

Paid time off

Zusammenfassung

Syneos Health is seeking an Experienced Clinical Research Associate, regionally aligned across the United States. You will perform site qualification, initiation, monitoring, and close-out visits, remotely or on-site, ensuring regulatory and protocol compliance.

This role requires up to 75% travel, strong communication skills, and knowledge of ICH/GCP guidelines. You will collaborate with site staff to drive data integrity and patient safety.

Qualifikationen

• Bachelor's degree or RN in a related field.
• Knowledge of Good Clinical Practice/ICH guidelines and other regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage travel up to 75% on a regular basis.

Aufgaben

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote).
• Verifies informed consent documentation and protects patient confidentiality.
• Reviews site processes, conducts source data review, and ensures CRF data accuracy.
• Manages IP inventory, labeling, and storage per protocol.
• Maintains ISF and TMF, archiving essential documents per guidelines.
• Documents activities and supports recruitment and retention efforts.
• Participates in sponsor meetings and training sessions; supports audit readiness.

Kenntnisse

Communication skills

GCP knowledge

Computer literacy

Travel readiness

Ausbildung

Bachelor's degree or RN in related field

Jobbeschreibung

Syneos Health is seeking an Experienced Clinical Research Associate, regionally aligned across the United States. You will perform site qualification, initiation, monitoring, and close-out visits, remotely or on-site, ensuring regulatory and protocol compliance.

This role requires up to 75% travel, strong communication skills, and knowledge of ICH/GCP guidelines. You will collaborate with site staff to drive data integrity and patient safety.