Remote Clinical Research Associate: Site Monitoring

Syneos Health, Inc.

Maryland

On-site

USD 85,000 - 125,000

Full time

3 days ago
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Benefits offered by this job

Company car or car allowance
Health benefits
401k match
Employee stock purchase plan
Bonus opportunities
Paid time off

Job summary

Syneos Health, Inc. seeks an Experienced Clinical Research Associate to support regionally aligned monitoring across the US. The role involves site qualification, initiation, monitoring, and close-out visits, ensuring regulatory and protocol compliance while maintaining data integrity.

The position emphasizes collaboration with investigators and cross-functional teams. You will support site management, IP inventory, and trial master file reconciliation, with extensive travel and a focus on audit

Qualifications

  • Bachelor's degree or RN in related field.
  • Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements.
  • Good computer skills and ability to learn new technologies.
  • Excellent communication, presentation and interpersonal skills.
  • Ability to travel up to 75%.

Responsibilities

  • Performs site qualification, initiation, interim monitoring and close-out visits on-site or remotely.
  • Verifies informed consent and protects confidentiality; assesses patient safety and data integrity.
  • Reviews ISF and TMF, tracks documentation and supports recruitment strategies.
  • Manages site processes per CMP/SMP, drives query resolution and data quality.
  • Coordinates IP inventory, labeling, storage and distribution per protocol.
  • Attends investigator meetings and supports audit readiness and training.

Skills

Excellent communication
Presentation skills
Interpersonal skills
Good computer skills
Travel up to 75%

Education

Bachelor's degree or RN

Job description

Syneos Health, Inc. seeks an Experienced Clinical Research Associate to support regionally aligned monitoring across the US. The role involves site qualification, initiation, monitoring, and close-out visits, ensuring regulatory and protocol compliance while maintaining data integrity.

The position emphasizes collaboration with investigators and cross-functional teams. You will support site management, IP inventory, and trial master file reconciliation, with extensive travel and a focus on audit

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