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.
- Work hours 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.
Responsibilities:
- Serve as Principal Investigator across high-quality clinical trials in major therapeutic indications (including diabetes, hypertension, COPD, obesity, depression, pain, Alzheimer’s, 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.
We are seeking a dedicated PI to launch a clinical research site in any of the following locations:
- Georgia - Columbus, Augusta, Savannah
- North Carolina - Charlotte, Raleigh, Greensboro, Durham, Winston-Salem, Cary
- South Carolina - Charleston, Columbia
- Tennessee - Memphis, Knoxville, Chattanooga, Clarksville, Murfreesboro
- Virginia - Virginia Beach, Chesapeake, Arlington, Richmond, Norfolk, Newport News, Alexandria
- Louisiana - New Orleans, Baton Rouge
- Alabama - Huntsville, Mobile, Birmingham, Montgomery
- Arkansas - Little Rock
- Mississippi - Jackson
Qualifications:
- MD or DO with active medical license in relevant state(s).
- 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.
