Senior CRA: Oncology Site Monitoring & Study Leadership

Parexel

Atlanta (GA)

In loco

USD 95.000 - 130.000

Tempo pieno

5 giorni fa
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Descrizione del lavoro

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in the United States (Atlanta area). The Sr.

CRA will oversee site management, monitoring, and close-out across assigned trials to ensure patient safety and quality of study execution in line with GCP and sponsor standards. Travel and collaboration with SCP and study team are essential. The role emphasizes monitoring, data integrity, and investigator site engagement, with responsibilities spanning site activation to close-out and

Competenze

  • Minimum 3 years monitoring experience in clinical research at CRO or pharma
  • Preferred Oncology therapeutic area experience
  • Global clinical trial experience preferred
  • Extensive knowledge of ICH/GCP, FDA regulations and local country rules
  • Must be fluent in English and local country language(s)
  • Travel 60-80% within area required
  • Valid driver’s license and passport required

Mansioni

  • Ensure proper conduct of clinical trials per SMP, laws, GCP and sponsor standards
  • Manage site activation through database lock with timelines and quality
  • Be primary contact for investigator sites; coordinate with SCP
  • Facilitate information flow between study team, vendors and sites
  • Coach and train site personnel to ensure protocol compliance and patient safety
  • Attend investigator meetings and provide enrollment support for site activation

Conoscenze

Monitoring experience
Oncology experience
Global trials
GCP/I CH knowledge
English fluency
Travel readiness
Driver’s license

Formazione

Bachelor’s degree in life sciences

Descrizione del lavoro

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in the United States (Atlanta area). The Sr.

CRA will oversee site management, monitoring, and close-out across assigned trials to ensure patient safety and quality of study execution in line with GCP and sponsor standards. Travel and collaboration with SCP and study team are essential. The role emphasizes monitoring, data integrity, and investigator site engagement, with responsibilities spanning site activation to close-out and

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