Principal Investigator

Location:

Rio Grande Valley Area (McAllen, Edinburg, Mission, Brownsville)

Engagement Type:

Independent Contractor | Per-Study /

As-Needed Specialties of Interest:

Internal Medicine, Family Medicine, Metabolic Disease, Geriatrics, Endocrinology, Cardiology, Infectious Disease, Women's Health, Pain Management, or Related Fields About Us We are building a next-generation clinical trials network that transforms community pharmacies into high-performing clinical trial sites. Our model expands patient access, accelerates enrollment, and enables sponsors to run efficient, decentralized and hybrid trials. As we activate pharmacy sites nationwide, we are seeking experienced Principal Investigators (PIs) to support study start-up, regulatory submissions, and trial oversight on a non-full-time, per-study basis. The Opportunity This role is ideal for physicians who: Want to participate in clinical research without full-time site commitments Are interested in innovative, pharmacy-embedded trial models Prefer flexible, study-based engagement PI engagement occurs both during the pre-award submission phase and post-award study execution, with scope and compensation defined per study. Key Responsibilities Serve as Principal Investigator of record for assigned pharmacy-based clinical trials Participate in pre-award study activities, including protocol review, feasibility assessments, and initial study applications and regulatory submissions (e.g., IRB, sponsor, FDA as applicable) Provide medical and scientific input during sponsor and CRO site selection and feasibility reviews Support development and execution of regulatory-ready site documentation prior to trial award Oversee trial conduct post-award, ensuring compliance with

ICH-GCP, FDA

regulations, and sponsor requirements Provide ongoing medical oversight and safety supervision throughout the study lifecycle Collaborate with pharmacists, study coordinators, sponsors, and CRO partners to ensure protocol adherence and data integrity Participate in investigator meetings and study-related reviews (primarily virtual; on-site as needed) Contribute to continuous improvement of pharmacy-embedded clinical research workflows Qualifications MD or DO (required) Active, unrestricted U.S. medical license Prior experience as a Principal Investigator or Sub-Investigator Strong knowledge of GCP and clinical trial regulations Comfortable working with decentralized / hybrid trial models Ability to engage on a per-study, non-full-time basis What We Offer Flexible, per-study compensation No full-time site burden Opportunity to shape an innovative pharmacy-based clinical trials ecosystem Access to a growing pipeline of industry-sponsored and investigator-initiated studies Long-term collaboration as our network scales nationally How to Apply Interested candidates should submit the details below to: contact@zorarxtrials.com CV