Clinical Trials Regulatory Lead

Ochsner Health

New Orleans (LA)

Presencial

USD 90 000 - 130 000

Tempo integral

Há 8 dias

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

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Resumo da oferta

Ochsner Health in New Orleans is seeking a skilled professional to independently manage and coordinate all aspects of clinical trials. You will work with research management and the Principal Investigator to ensure regulatory compliance and successful study start-up across departments.

Candidates should have 3 years of trial experience in a clinical setting, or 2 years with ACRP or SOCRA certification, along with strong critical thinking, Epic knowledge, and excellent communication.

Qualificações

  • Strong critical thinking and knowledge of clinical research terminology.
  • Ability to coordinate regulatory processes for trials and audits.
  • Experience with grant and budget development
  • Proficiency with computers, software and Epic
  • Excellent written and verbal communication skills

Responsabilidades

  • Manage research activities for clinical trials and data management and enable successful study start-up.
  • Maintain study compliance and participate in audits and regulatory reviews.
  • Oversee data management and lead special projects and tracking.
  • Maintain strong relationships with study sponsors.
  • Pursue opportunities for ongoing education in research.
  • Perform other related duties as assigned.

Conhecimentos

Critical thinking
Regulatory knowledge
Clinical research terminology
Verbal and written communication
Organization and multitasking
Travel flexibility

Formação académica

High school diploma or equivalent
ACRP or SOCRA certification

Ferramentas

Epic

Descrição da oferta de emprego

Ochsner Health in New Orleans is seeking a skilled professional to independently manage and coordinate all aspects of clinical trials. You will work with research management and the Principal Investigator to ensure regulatory compliance and successful study start-up across departments.

Candidates should have 3 years of trial experience in a clinical setting, or 2 years with ACRP or SOCRA certification, along with strong critical thinking, Epic knowledge, and excellent communication.

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