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 - only 2-3 partial days per week!
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.
Location:
Canton, GA
Qualifications:
MD or DO with active medical license in relevant state(s), Primary Care Physician/Internist strongly preferred.
Experience as a PI or Sub-Investigator in FDA-regulated clinical trials required.
Strong clinical judgment and leadership presence.
Passion for advancing clinical science without the red tape.