Remote Field Senior Clinical Research Associate

North American Science Associates, Inc.; Northern (KY); Teletrabalho; USD 69 000 - 134 000; Tempo integral

Resumo da oferta

North American Science Associates, Inc. (NAMSA) is seeking a Senior Clinical Research Associate for remote USA work. The role focuses on maintaining human subject protection, GCP, and regulatory compliance while coordinating site monitoring across studies.

The candidate should have a higher education degree and 5+ years in clinical trials, with 3+ years in monitoring and 1 year device trial experience. SoCRA/ACRP certification is a plus. Travel up to 80% may be required.

Qualificações

• Fluency in English and local language, if different, required.
• Higher education degree or equivalent education, training, and experience.
• Preferred 5 years clinical trial experience.
• Preferred 3 years monitoring experience.
• Preferred 1 year device trial experience.
• Certifications such as SoCRA or ACRP preferred but not required.

Responsabilidades

• Works on assigned studies to ensure human subject protection, GCP, and regulations.
• Coordinates and manages clinical site monitoring for assigned studies.
• May conduct on-site and remote monitoring visits.
• Serve as primary point of contact for site questions.
• Communicates site performance, trends, and concerns to study team.
• Supports study start-up activities and quality review of documents.
• Performs study-related training and maintains study documents.
• Tracks site and study metrics including enrollment and deviations.
• Participates in meetings with prospective clients and mentors CRAs.

Conhecimentos

Fluency in English

Higher education degree

5 years clinical trial experience

3 years monitoring experience

1 year device trial experience

Certification (SoCRA/ACRP) preferred

Formação académica

Bachelor's degree or equivalent

Descrição da oferta de emprego

North American Science Associates, Inc. (NAMSA) is seeking a Senior Clinical Research Associate for remote USA work. The role focuses on maintaining human subject protection, GCP, and regulatory compliance while coordinating site monitoring across studies.

The candidate should have a higher education degree and 5+ years in clinical trials, with 3+ years in monitoring and 1 year device trial experience. SoCRA/ACRP certification is a plus. Travel up to 80% may be required.