Senior Clinical Research Associate - Remote & Regional Lead

Syneos Health, Inc.

Salem (OR)

Remote

USD 65,000 - 95,000

Full time

8 days ago

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Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to be regionally aligned across the US. The CRA will monitor sites, ensure ICH-GCP compliance, manage essential documents, and support data integrity across trials.

The role requires a Bachelor's degree or RN, strong communication skills, and the ability to travel up to 75% to site locations. You will collaborate with sponsors and cross-functional teams to deliver high-quality clinical research outcomes.

Qualifications

  • Bachelor's degree or RN in a related field or equivalent combination of education, training and experience.
  • Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
  • Strong computer skills and ability to adapt to new technologies.
  • Excellent communication, presentation and interpersonal skills.
  • Ability to travel up to 75% on a regular basis.

Responsibilities

  • Performs site qualification, initiation, monitoring, management and close-out visits (on-site or remote) ensuring regulatory and protocol compliance.
  • Verifies informed consent and protects subject confidentiality and data integrity.
  • Conducts source data review and ensures accurate data entry and timely query resolution.
  • Manages IP inventory, reconciliation, and storage per protocol.
  • Maintains ISF/TMF accuracy and supports audit readiness and site training.

Skills

Communication skills
Computer skills
GCP knowledge
Travel readiness
Regulatory awareness

Education

Bachelor's degree or RN

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to be regionally aligned across the US. The CRA will monitor sites, ensure ICH-GCP compliance, manage essential documents, and support data integrity across trials.

The role requires a Bachelor's degree or RN, strong communication skills, and the ability to travel up to 75% to site locations. You will collaborate with sponsors and cross-functional teams to deliver high-quality clinical research outcomes.

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