Senior Clinical Research Associate - Remote (US)

Syneos Health/ inVentiv Health Commercial LLC

Arizona

Remote

USD 70,000 - 110,000

Full time

11 days ago

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Job summary

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) with at least one year of independent monitoring experience for a homebased role in the United States. You will perform site qualification, initiation, interim monitoring and close-out visits, ensuring regulatory compliance and high data quality while supporting study deliverables.

This position requires strong communication, computer literacy, and the ability to travel as needed.

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 travel up to 75% on a regular basis.

Responsibilities

  • 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 subject confidentiality; assesses safety and data integrity at investigator sites.
  • Reconciles ISF with TMF, ensures archiving of essential documents; supports audit readiness and site training.
  • Manages IP inventory, labeling, storage, and release according to protocol; monitors IP dispatch and administration.
  • Maintains data capture quality; conducts source data verification and query resolution within timelines.

Skills

GCP/ICH Guidelines
Communication skills
Interpersonal skills
Computer skills

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) with at least one year of independent monitoring experience for a homebased role in the United States. You will perform site qualification, initiation, interim monitoring and close-out visits, ensuring regulatory compliance and high data quality while supporting study deliverables.

This position requires strong communication, computer literacy, and the ability to travel as needed.

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