TransPerfect is hiring a
Principal Investigator

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TransPerfect

πŸ’΅ ~$30k
πŸ“Remote - United States

Summary

The job is for a Principal Investigator with a medical degree (preferably cardiology or internal medicine specializing in hypertension or cardiovascular disease) to manage the IRB process for a high blood pressure data collection study. The position is remote and on an independent contractor basis, with a total estimated workload of 108 hours.

Requirements

  • Doctor of Medicine (MD) - cardiology or internal medicine with a specialization in hypertension or cardiovascular disease
  • Proven research experience in managing the IRB submission and approval process for clinical studies
  • In-depth understanding of ethical and regulatory requirements governing clinical research
  • Excellent communication skills, with the ability to convey complex regulatory concepts to diverse audiences
  • Strong interpersonal skills and the ability to work effectively in a collaborative team environment

Responsibilities

  • Manage the entire IRB submission process, ensuring timely and accurate completion of all required documentation
  • Collaborate with regulatory affairs specialists to address any queries or modifications requested by the IRB
  • Work closely with multidisciplinary teams to conceptualize and design research studies, ensuring alignment with ethical and regulatory guidelines
  • Stay abreast of relevant regulations and guidelines, ensuring the study's compliance throughout its lifecycle
  • Provide guidance to the research team on ethical conduct and regulatory adherence
  • Facilitate communication between the research team, regulatory authorities, and IRB members
  • Work collaboratively with external partners, ensuring a smooth regulatory process
  • Maintain accurate and organized records related to the IRB submission and approval process
  • Ensure that all study documentation is in accordance with regulatory standards
  • Provide support and guidance to on-site investigators and clinical staff regarding ethical and regulatory policies
  • Collaborate with the research team to address any regulatory challenges that may arise during the study

Preferred Qualifications

Previous involvement in research related to hypertension or cardiovascular disease is highly desirable

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