Principal Investigator [Part or Full Time]
West Monroe, LAFull-time and Part-time
Behavioral Health Market Context
Apply Nowvia Indeed
Benefits
Health Insurance
Job Description
nships, 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.
Locations:
• Canton, GA
• Atlanta, GA
• Jacksonville, FL
• Miami, FL
• Knoxville, TN
• Jefferson City / Morrisville, TN
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.
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.
Locations:
• Canton, GA
• Atlanta, GA
• Jacksonville, FL
• Miami, FL
• Knoxville, TN
• Jefferson City / Morrisville, TN
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.
Qualifications
- •Transparent communication and rapid study startup cycles - no waiting months to activate
- •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
Benefits
- •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
- •You’ll have a full-time regulatory and coordinator team supporting you
- •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
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