Principal Investigator

Position: Principal Investigator [Full Time]
About Us
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. 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. It operates a hybrid model of free-standing and physician embedded sites. 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. The network is a preferred partner to leading global pharma and biotech customers.
People First Humility Integrity One Team Results Accountability

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.
What Makes This Different:Youll 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.
Responsibilities:Serve as Principal Investigator across high-quality clinical trials in major therapeutic indications (including diabetes, hypertension, COPD, obesity, depression, pain, Alzheimers, and infectious diseases).Ensure adherence to GCP and study protocols while collaborating with cross-functional research teams.

Provide medical oversight during all trial phases, including patient eligibility review, safety assessments, and data validation.

Contribute to internal scientific discussions, quality improvement, and site expansion opportunities.
Location:Jacksonville, FL
Qualifications:MD or DO with active medical license in relevant state(s), Internist strongly preferred.
2+ years of experience as a PI or Sub-Investigator in FDA-regulated clinical trials.

Strong clinical judgment and leadership presence.

Passion for advancing clinical science without the red tape.

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