Rovia

Rovia

Principal Investigator [Part Time]

Miami, FL · Principal · Part-time

Sponsorship not specifiedDetected 20 days ago
GCPClinical TrialsClinical ResearchPatient CareResearchLeadershipCommunication

About the role

  • It operates a hybrid model of free-standing and physician embedded sites.

Responsibilities

  • Own a private practice within the state of Florida.

Nice to have

  • Our sites operate with streamlined systems, dedicated coordinator teams, and strong sponsor relationships, so our investigators can focus on advancing medicine - not chasing paperwork.
  • Rovia is a clinical research site network with 18+ years of experience.
  • Across its 15 sites and 80+ investigators, Rovia has a proven history of enrolling patients with best-in class retention, rapid study-start up and high-quality data.
  • People First - Humility - Integrity - One Team - Results Accountability
  • PI or Sub-I experience preferred.

Benefits

  • A strong compensation package including sign-on bonus and performance bonuses.
  • Provide medical oversight during all trial phases, including patient eligibility review, safety assessments, and data validation.

Company info

  • At Rovia Clinical Research, we practice Research with Kindness!
  • We eliminate the administrative roadblocks, delayed study startups, and under-resourced support that keep great researchers from focusing on what truly matters - scientific leadership, patient impact, and clinical innovation.
  • The network is a preferred partner to leading global pharma and biotech customers.
  • We are seeking a motivated and experienced physician to join our clinical research team as a Principal Investigator.
  • Rovia is offering: A strong compensation package including sign-on bonus and performance bonuses.
  • Operational autonomy and empowerment to focus on patient care and medical decision-making - corporate resources behind you - no underfunded sites or bureaucratic micromanagement. < 10 hours per week to accommodate work/life balance.
  • What Makes This Different: You'll have a full-time regulatory and coordinator team supporting you.
  • Transparent communication and rapid study startup cycles - no waiting months to activate.
  • A patient recruitment infrastructure that delivers enrolled participants on time.

Visa & Work Authorization

  • Our sites operate with streamlined systems, dedicated coordinator teams, and strong sponsor relationships, so our investigators can focus on advancing medicine - not chasing paperwork.

This listing is sourced directly from Rovia's careers page and normalized into a canonical job model.