Principal Investigator (Clinical Research Physician) - Charlotte, NC 245987
Medix
240K–270K a year
Behavioral Health Market Context
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Job Description
le and supportive environment.
Job Responsibilities: Key Responsibilities:
Serve as the Principal Investigator on clinical trials across multiple therapeutic areas
Conduct medical evaluations and assessments for study participants
Ensure compliance with FDA, GCP, and other regulatory requirements
Review and approve essential study documents, including informed consent forms and medical histories
Oversee participant safety and manage adverse events with the research team
Collaborate with sponsors, CROs, and internal staff to meet study goals and timelines
Provide medical oversight to coordinators and research personnel
Contribute to identifying and developing new clinical trial opportunities
Qualifications: Qualifications
MD or DO with Board Certification or Eligibility in Internal Medicine, Family Medicine, or a related field
Active North Carolina medical license (or ability to obtain)
Clinical experience in general medicine; clinical research experience is a plus but not required
Solid understanding of clinical diagnostics, pharmacology, and patient care standards
Strong communication and leadership skills
Commitment to ethical research practices and patient safety
Working Hours: Full Time
Mon - Fri 8 AM - 5 PM
Job Responsibilities: Key Responsibilities:
Serve as the Principal Investigator on clinical trials across multiple therapeutic areas
Conduct medical evaluations and assessments for study participants
Ensure compliance with FDA, GCP, and other regulatory requirements
Review and approve essential study documents, including informed consent forms and medical histories
Oversee participant safety and manage adverse events with the research team
Collaborate with sponsors, CROs, and internal staff to meet study goals and timelines
Provide medical oversight to coordinators and research personnel
Contribute to identifying and developing new clinical trial opportunities
Qualifications: Qualifications
MD or DO with Board Certification or Eligibility in Internal Medicine, Family Medicine, or a related field
Active North Carolina medical license (or ability to obtain)
Clinical experience in general medicine; clinical research experience is a plus but not required
Solid understanding of clinical diagnostics, pharmacology, and patient care standards
Strong communication and leadership skills
Commitment to ethical research practices and patient safety
Working Hours: Full Time
Mon - Fri 8 AM - 5 PM
Qualifications
- •MD or DO with Board Certification or Eligibility in Internal Medicine, Family Medicine, or a related field
- •Active North Carolina medical license (or ability to obtain)
- •Solid understanding of clinical diagnostics, pharmacology, and patient care standards
- •Strong communication and leadership skills
- •Commitment to ethical research practices and patient safety
Benefits
Responsibilities
- •Serve as the Principal Investigator on clinical trials across multiple therapeutic areas
- •Conduct medical evaluations and assessments for study participants
- •Ensure compliance with FDA, GCP, and other regulatory requirements
- •Review and approve essential study documents, including informed consent forms and medical histories
- •Oversee participant safety and manage adverse events with the research team
- •Collaborate with sponsors, CROs, and internal staff to meet study goals and timelines
- •Provide medical oversight to coordinators and research personnel
- •Contribute to identifying and developing new clinical trial opportunities
- •Working Hours: Full Time
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