Clinical Research Associate – Remote Across US

Syneos Health, Inc.; Vermont; On-site; USD 75,000 - 100,000; Full time

Benefits offered by this job

Health benefits

Company car or car allowance

401k matching

Job summary

Syneos Health, Inc. seeks an Experienced Clinical Research Associate to support site qualification, initiation, monitoring and close-out visits across the US. You will verify consent, protect patient data, review source documents and ensure data accuracy in CRFs while maintaining regulatory compliance.

You'll collaborate with sponsor teams, attend investigator meetings and help ensure audits readiness. A strong background in GCP/ICH and travel readiness up to 75% is essential.

Qualifications

• Bachelor's degree or RN in a related field or equivalent experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements.
• Strong computer skills and ability 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, initiation, interim monitoring and close-out visits.
• Verifies informed consent and protects subject confidentiality.
• Assesses site processes and conducts source data review.
• Ensures accurate data entry in CRF and resolves queries.
• May manage IP inventory and ensure proper labeling and release.
• Maintains ISF and TMF reconciliation; supports audit readiness.
• Communicates with sites, sponsors and team members to meet timelines.
• Participates in investigator meetings and training sessions.

Skills

GCP knowledge

Computer skills

Communication skills

Travel up to 75%

Education

Bachelor's degree or RN in a related field

Job description

Syneos Health, Inc. seeks an Experienced Clinical Research Associate to support site qualification, initiation, monitoring and close-out visits across the US. You will verify consent, protect patient data, review source documents and ensure data accuracy in CRFs while maintaining regulatory compliance.

You'll collaborate with sponsor teams, attend investigator meetings and help ensure audits readiness. A strong background in GCP/ICH and travel readiness up to 75% is essential.