Regional Clinical Research Associate — Remote/Onsite

Syneos Health, Inc.

Kentucky

Vor Ort

USD 90.000 - 130.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Company car or car allowance
Medical, Dental and Vision benefits
401k match
Employee Stock Purchase Plan
Bonus eligibility
Flexible PTO and sick time

Zusammenfassung

Syneos Health is seeking an Experienced Clinical Research Associate focused on regionally aligned monitoring across the US. The role emphasizes site qualification, initiation, monitoring, and close-out with a strong emphasis on regulatory compliance and patient safety.

You will collaborate with study teams, ensure data integrity, support site training, and coordinate with sponsor meetings. Travel up to 75% is required, with a dynamic field-based environment and ongoing professional development.

Qualifikationen

  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
  • Excellent communication, presentation and interpersonal skills.
  • Ability to manage required travel of up to 75% on a regular basis.

Aufgaben

  • Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely).
  • Verifies informed consent, protects confidentiality and assesses factors affecting subject safety and data integrity.
  • Reconciles site documents, monitors ISF vs TMF and ensures audit readiness.
  • Supports subject recruitment and data tracking; ensures adherence to CMP/SMP and regulatory requirements.

Kenntnisse

Good Clinical Practice knowledge
Excellent communication
Adaptability to travel

Ausbildung

Bachelor's degree or RN in a related field or equivalent

Jobbeschreibung

Syneos Health is seeking an Experienced Clinical Research Associate focused on regionally aligned monitoring across the US. The role emphasizes site qualification, initiation, monitoring, and close-out with a strong emphasis on regulatory compliance and patient safety.

You will collaborate with study teams, ensure data integrity, support site training, and coordinate with sponsor meetings. Travel up to 75% is required, with a dynamic field-based environment and ongoing professional development.

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