Principal Investigator

Location:TEXAS (Hybrid)Engagement Type: Independent Contractor | Per-Study / As-NeededSpecialties of Interest: Internal Medicine, Family Medicine, Metabolic Disease, Geriatrics, Endocrinology, Cardiology, Infectious Disease, Women's Health, Pain Management, or Related FieldsAbout UsWe 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 OpportunityThis role is ideal for physicians who:Want to participate in clinical research without full-time site commitmentsAre interested in innovative, pharmacy-embedded trial modelsPrefer flexible, study-based engagementPI engagement occurs both during the pre-award submission phase and post-award study execution, with scope and compensation defined per study.Key ResponsibilitiesServe as Principal Investigator of record for assigned pharmacy-based clinical trialsParticipate 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 reviewsSupport development and execution of regulatory-ready site documentation prior to trial awardOversee trial conduct post-award, ensuring compliance with ICH-GCP, FDA regulations, and sponsor requirementsProvide ongoing medical oversight and safety supervision throughout the study lifecycleCollaborate with pharmacists, study coordinators, sponsors, and CRO partners to ensure protocol adherence and data integrityParticipate in investigator meetings and study-related reviews (primarily virtual; on-site as needed)Contribute to continuous improvement of pharmacy-embedded clinical research workflowsQualificationsMD or DO (required)Active, unrestricted U.S. medical licensePrior experience as a Principal Investigator or Sub-InvestigatorStrong knowledge of GCP and clinical trial regulationsComfortable working with decentralized / hybrid trial modelsAbility to engage on a per-study, non-full-time basisWhat We OfferFlexible, per-study compensationNo full-time site burdenOpportunity to shape an innovative pharmacy-based clinical trials ecosystemAccess to a growing pipeline of industry-sponsored and investigator-initiated studiesLong-term collaboration as our network scales nationallyHow to ApplyInterested candidates should submit the details below to: contact@CV

Created: 2026-05-08