Principal Investigator
alsaresearch
healthcare

research

Job Description:

Daily Responsibilities:

As a Principal Investigator, you will lead and oversee clinical research studies across various therapeutic areas. This role offers the unique opportunity to generate additional revenue and increase your earning potential by conducting clinical research, with full operational and administrative support provided by our organization. The PI will play a critical role in leading studies, ensuring regulatory compliance, and overseeing patient safety. Expand Your Career � Diversify your professional experience while maintaining your medical practice. Play a key role in bringing new treatments to market and provide patients with access to cutting-edge therapies. Earn Additional Revenue � Generate additional revenue while maintaining your existing clinical practice. Serving as a PI allows you to maximize income with minimal disruption to your schedule. We offer competitive compensation based on a profit-sharing model from each clinical research study you participate in as a Principal or Sub Investigator. Full Support Provided � No prior research experience needed�our team manages the logistics. We handle regulatory compliance, patient recruitment, study coordination, and administrative tasks so you can focus on the research itself. Work Flexibility � Typical demand is 5-10 hours per week, per study. Study activities can often be completed in a single day with additional scheduling options available. Some tasks can be done remotely. Location � We are seeking candidates in the Southwestern Connecticut area.

Job Requirements:

KEY RESPONSIBILITIES Provide Medical Oversight & Ensure Patient Safety Serve as the lead physician for clinical trials, ensuring patient safety and ethical study conduct. Review study protocols and monitor patient health, while our experienced research team handles day-to-day operations. Ensure Compliance with Regulatory & Ethical Guidelines Maintain Good Clinical Practice (GCP) standards and oversee informed consent. Work with our regulatory team, which manages all paperwork, IRB approvals, and reporting. Collaborate with Sponsors & Research Teams Work with pharmaceutical companies and CROs to oversee study progress and outcomes. Provide medical expertise while our research coordinators handle patient recruitment, scheduling, and data collection. Engage in Groundbreaking Research with Minimal Disruption to Your Practice Play a role in advancing medicine while maintaining your regular clinical duties. Provide patients with access to cutting-edge treatments without adding extra administrative burden.

Compensation:

Competitive compensation and revenue-sharing opportunities. Full operational and administrative support for clinical trials. The opportunity to expand your practice and professional expertise with us Professional development and career growth opportunities. Flexible work schedule Job Type: Part-time Pay: $50,000.00 - $200,000.00 per year Benefits: Flexible schedule Experience: Clinical research: 2 years (Preferred) License/Certification: Medical License (Required) $50,000 - $200,000 per year

Job Location(s):

Stamford, Connecticut

Source:

Company Career Section

Competition:

N/A

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Yes

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