Remote Senior CRA - Contract, Clinical Trials Expert

Evolution Research Group

Maryland

Remoto

USD 90.000 - 130.000

Tempo pieno

6 giorni fa
Candidati tra i primi
Generatore di candidature

Trasforma questo annuncio in un colloquio — un curriculum e una lettera di presentazione creati in base a ciò questo datore di lavoro sta cercando.

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Descrizione del lavoro

Evolution Research Group is seeking a Contract Senior Clinical Research Associate to monitor clinical sites for multiple studies. Location: Maryland; remote options for US contract; travel up to 100%.

The CRA will ensure protocol adherence, maintain study documentation, train site staff, and manage investigator site files, with emphasis on quality data and regulatory compliance. A Bachelor's in life sciences and 5 years CRA experience are required.

Competenze

  • Bachelor's degree in life sciences or healthcare with at least 5 years of field CRA experience.
  • Valid driver’s license and ability to travel up to 100%.
  • Legally authorized to work in the US as an independent contractor (LLC or INC.) or through an agency.
  • Proficiency with electronic CRF platforms and data capture systems.

Mansioni

  • Manage and monitor site activities for assigned clinical studies.
  • Ensure protocol adherence and compliance with FDA regulations and ICH-GCP.
  • Coordinate communication with investigative sites and data management teams.
  • Maintain audit-ready Investigator Site File and Trial Master File documentation.
  • Perform study initiation and close-out activities and train site staff.

Conoscenze

GCP compliance
ICH guidelines
Clinical trials
Electronic CRF
Interpersonal skills
Organizational skills
Attention to detail
Independent work
Travel readiness

Formazione

Bachelor's degree in life sciences/healthcare

Descrizione del lavoro

Evolution Research Group is seeking a Contract Senior Clinical Research Associate to monitor clinical sites for multiple studies. Location: Maryland; remote options for US contract; travel up to 100%.

The CRA will ensure protocol adherence, maintain study documentation, train site staff, and manage investigator site files, with emphasis on quality data and regulatory compliance. A Bachelor's in life sciences and 5 years CRA experience are required.

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