Job Description
ABOUT USWe are an independent clinical research site dedicated to advancing medicine through high-quality clinical trials. With a hands-on approach and a commitment to long-term success, we provide full operational support to ensure seamless trial executionallowing physicians to focus on patient care and innovation. We are seeking to partner with physicians to serve as Principal Investigators on clinical trials.POSITION OVERVIEWAs 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.OPPORTUNITY HIGHLIGHTSExpand 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 neededour 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.KEY RESPONSIBILITIESProvide Medical Oversight & Ensure Patient SafetyServe 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 GuidelinesMaintain 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 TeamsWork 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 PracticePlay a role in advancing medicine while maintaining your regular clinical duties.Provide patients with access to cutting-edge treatments without adding extra administrative burden.What you DON'T have to worry about as a PI working with us:We take care of the operational and administrative tasks so you can focus on patient care and medical oversight. As a Principal Investigator, you wont need to worry about:Regulatory & Compliance Paperwork Our team handles IRB approvals, submissions, and reporting.Recruitment & Enrollment We provide dedicated recruitment and retention support to ensure a smooth patient enrollment process.Study Logistics & Data Management Our trained research coordinators manage study flow, patient visits, and data collection.This is a low-burden, high-reward opportunity to expand your professional experience, contribute to groundbreaking research, and increase your earnings potentialall while maintaining your existing practice.QUALIFICATIONSEducation: MD or DO (any specialty)experience with clinical trials/research is strongly preferred.Certification: A board certification is requiredExperience: Minimum of 2 years in clinical research (as a PI or Sub-Investigator) strongly preferred. Experience in psychiatry, CNS, metabolic disorders, infectious disease, immunology, or other relevant areas is a plus.Skills: Strong knowledge of clinical research methodologies, regulatory requirements, and GCP. Excellent analytical, organizational, and communication skills.Attributes: Detail-oriented, able to work independently and as part of a collaborative team, strong leadership skills, and a commitment to advancing medical research.WHAT WE OFFERCompetitive compensation and revenue-sharing opportunities.Full operational and administrative support for clinical trials.The opportunity to expand your practice and professional expertise with usProfessional development and career growth opportunities.Flexible work scheduleJob Type: Part-timePay: $50,000.00 - $200,000.00 per yearBenefits:Flexible scheduleExperience:Clinical research: 2 years (Preferred)License/Certification:Medical License (Required)Ability to Commute:Stamford, CTWork Location: In person
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ALSA Research
Job Tags
Remote work, Flexible hours, 10 hours per week,