Remote Senior Clinical Research Associate - Sponsor Focus

Syneos Health, Inc.

North Carolina

Hybrid

USD 85,000 - 120,000

Full time

14 days+
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Job summary

Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated work. The role operates remotely within the United States and supports site qualification, initiation, monitoring, and close-out activities in accordance with ICH-GCP and study protocol.

You will verify informed consent, protect patient confidentiality, and assess safety and data integrity. The job involves CMP/SMP adherence, source document review, CRF data checks, and IP inventory management to ensure

Qualifications

  • Experience with clinical monitoring and site management activities.
  • Familiarity with ICH-GCP guidelines and regulatory requirements.
  • Ability to review source documents and ensure data accuracy.

Responsibilities

  • Performs site qualification, initiation, interim monitoring, management and close-out visits (on-site or remote) with regulatory and protocol compliance.
  • Verifies informed consent processes and protects subject confidentiality; assesses safety and data integrity implications.
  • Conducts CMP/SMP-based assessments, source document review, CRF data accuracy checks, and supports query resolution remotely and on-site.
  • Manages IP inventory, labeling, storage, and reconciliation per protocol requirements.
  • Routinely reviews ISF accuracy and reconciles with Trial Master File.

Skills

ICH-GCP knowledge
Regulatory compliance
Site management
Data review
Source Document Review
IP inventory

Job description

Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated work. The role operates remotely within the United States and supports site qualification, initiation, monitoring, and close-out activities in accordance with ICH-GCP and study protocol.

You will verify informed consent, protect patient confidentiality, and assess safety and data integrity. The job involves CMP/SMP adherence, source document review, CRF data checks, and IP inventory management to ensure

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