Clinical Trial Principal Investigator - Onsite Lead

Care Access

Houston (TX)

On-site

USD 200,000 - 400,000

Full time

9 days ago

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Benefits offered by this job

PTO and holidays
Medical, dental, vision insurance
Health Savings Account
Short-Term & Long-Term Disability
401(k) with company match

Job summary

Care Access seeks a Principal Investigator in Houston, TX to oversee all clinical trials per study protocols, company processes, and GCP. This on-site role requires medical licensure, PI experience, and ability to train staff and ensure participant safety.

You will lead medical review, oversee monitoring visits, and collaborate with sponsors to ensure adherence to regulatory standards and trial integrity.

Qualifications

  • Excellent written and verbal communication skills.
  • Ability to effectively prioritize tasks in a fast-paced environment.
  • Attention to detail and ability to maintain confidentiality when handling sensitive information.
  • Critical thinking and dynamic problem-solving skills.

Responsibilities

  • Provide overall medical oversight and review of protocols in conformance with good clinical practice.
  • Ensure safety and well-being of all participants at the trial site; assess responses and address adverse events.
  • Perform physical assessments, examinations and study procedures per protocols.
  • Train Sub-Investigators and staff on protocol procedures and provide medical support.
  • Review inclusion/exclusion criteria and endpoints with the research team.
  • Comply with GCP and regulatory requirements; participate in monitoring visits and sponsor meetings.

Skills

Communication
Prioritization
Attention to detail
Critical thinking

Education

MD or DO

Job description

Care Access seeks a Principal Investigator in Houston, TX to oversee all clinical trials per study protocols, company processes, and GCP. This on-site role requires medical licensure, PI experience, and ability to train staff and ensure participant safety.

You will lead medical review, oversee monitoring visits, and collaborate with sponsors to ensure adherence to regulatory standards and trial integrity.

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