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Principal Investigator [Part or Full Time]

Rovia Clinical Research
Posted 4 months ago, valid for 15 days
Location

Morristown, Hamblen 37815, TN

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Rovia is seeking a motivated and experienced physician to join their clinical research team as a Principal Investigator with a strong compensation package, including a sign-on bonus and performance bonuses.
  • The position offers operational autonomy, allowing the physician to focus on patient care and medical decision-making without bureaucratic micromanagement.
  • Candidates should have at least 2 years of experience as a Principal Investigator or Sub-Investigator in FDA-regulated clinical trials.
  • The role involves serving as Principal Investigator across high-quality clinical trials in major therapeutic indications, ensuring adherence to GCP and study protocols.
  • An MD or DO with an active medical license is required, and the position is located in Jefferson City, TN.

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.

Location:

  • Jefferson City, TN

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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