Principal Investigator - Houston

Only for registered members Houston, United States

2 days ago

Default job background
$180,000 - $260,000 (USD) per year *
* This salary range is an estimation made by beBee
Company Description · Clear Path Clinical Research is a community-based clinical research site dedicated to conducting ethical, high-quality, and patient-centered clinical trials. Collaborating with sponsors, CROs, and investigators, we specialize in Phase II–IV studies while ens ...
Job description
Company Description
Clear Path Clinical Research is a community-based clinical research site dedicated to conducting ethical, high-quality, and patient-centered clinical trials.

Collaborating with sponsors, CROs, and investigators, we specialize in Phase II–IV studies while ensuring regulatory compliance, data integrity, and participant safety.

Our team strives for efficiency in study execution and fostering strong partnerships, aiming to deliver reliable results. Committed to inclusivity, we focus on enhancing access to research opportunities within diverse communities.
Role Description

This is a full-time hybrid role for a Principal Investigator based in Houston, TX, with the flexibility of partial work-from-home options.

The Principal Investigator will oversee the planning, execution, and monitoring of clinical trials while ensuring adherence to regulatory standards and ethical guidelines.

Responsibilities include supervising research staff, maintaining study documentation, managing participant safety, monitoring protocol compliance, and serving as the primary point of contact for sponsors and regulatory entities.

Qualifications
Strong knowledge of clinical research, regulatory requirements, and ethical practices related to Phase II–IV trials
Proven ability in leadership, team management, and collaboration with diverse stakeholders
Exceptional analytical, problem-solving, and critical thinking skills
Outstanding written and verbal communication skills, including preparation of study documentation and sponsor/partner engagement
Advanced degree in Medicine, Pharmacy, or a related field (e.g., MD, DO, PharmD, or PhD preferred)
Proficiency in managing study protocols, data integrity, and patient safety monitoring
Experience with community-based or diverse population clinical trials is a plus
Demonstrated commitment to ethical research practices and improving healthcare outcomes


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