Remote CRA – Full-Service Clinical Trials

Syneos Health, Inc.; Town of Texas (WI); Hybrid; USD 70,000 - 110,000; Full time

Job summary

Syneos Health is seeking a Clinical Research Associate - Full-Service to support site monitoring, data integrity and regulatory compliance across multiple trial sites. The role emphasizes remote monitoring, ensuring ICH-GCP alignment and accurate data capture, with travel up to 75% as required.

Ideal candidates hold a Bachelor's or RN in a related field, have strong knowledge of GCP/ICH guidelines, excellent communication skills, and proficiency with common computer tools.

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.
• 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.

Responsibilities

• 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 is adequately performed and documented; protects confidentiality and assesses factors affecting subject safety and data integrity.
• Conducts Source Document Review and ensures accurate data in CRFs; drives query resolution to closure within timelines.
• May perform IP inventory, reconciliation and ensure proper labeling, storage, and release.
• Maintains ISF and TMF, archives essential documents, and supports recruitment and tracking activities.

Skills

GCP/ICH knowledge

Excellent communication

Travel up to 75%

Computer skills

Clinical monitoring

Education

Bachelor's degree or RN in related field

Tools

Microsoft Office

Job description

Syneos Health is seeking a Clinical Research Associate - Full-Service to support site monitoring, data integrity and regulatory compliance across multiple trial sites. The role emphasizes remote monitoring, ensuring ICH-GCP alignment and accurate data capture, with travel up to 75% as required.

Ideal candidates hold a Bachelor's or RN in a related field, have strong knowledge of GCP/ICH guidelines, excellent communication skills, and proficiency with common computer tools.