Principal Investigator (MD)
Cedar Rapids, IAFull-time
Behavioral Health Market Context
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Job Description
ials within a fully supported research environment. The organization conducts Phase I through Phase IV clinical trials across multiple therapeutic areas and provides comprehensive operational, regulatory, and research staff support.
Multiple openings are available nationwide due to continued growth.
Key Responsibilities
• Serve as Principal Investigator on assigned clinical trials in compliance with ICH-GCP, FDA regulations, and sponsor protocols
• Oversee study conduct, subject safety, and data integrity
• Ensure protocol adherence and regulatory compliance
• Collaborate with Sub-Investigators, Study Coordinators, and research staff
• Participate in sponsor, CRO, and monitor visits as required
• Maintain accurate and complete regulatory documentation
Required Qualifications
• MD or DO degree
• Active, unrestricted medical license in the state where you reside and practice
• Board Certified or Board Eligible in Internal Medicine, Family Medicine, Rheumatology, or a related specialty
• No prior Principal Investigator or clinical research experience required
• Strong interest in clinical research and patient care
• Ability to meet required on-site time commitments
Preferred Experience (Not Required)
• Prior experience as a Principal Investigator or Sub-Investigator
• Familiarity with FDA-regulated clinical research environments
Multiple openings are available nationwide due to continued growth.
Key Responsibilities
• Serve as Principal Investigator on assigned clinical trials in compliance with ICH-GCP, FDA regulations, and sponsor protocols
• Oversee study conduct, subject safety, and data integrity
• Ensure protocol adherence and regulatory compliance
• Collaborate with Sub-Investigators, Study Coordinators, and research staff
• Participate in sponsor, CRO, and monitor visits as required
• Maintain accurate and complete regulatory documentation
Required Qualifications
• MD or DO degree
• Active, unrestricted medical license in the state where you reside and practice
• Board Certified or Board Eligible in Internal Medicine, Family Medicine, Rheumatology, or a related specialty
• No prior Principal Investigator or clinical research experience required
• Strong interest in clinical research and patient care
• Ability to meet required on-site time commitments
Preferred Experience (Not Required)
• Prior experience as a Principal Investigator or Sub-Investigator
• Familiarity with FDA-regulated clinical research environments
Qualifications
- •MD or DO degree
- •Active, unrestricted medical license in the state where you reside and practice
- •Board Certified or Board Eligible in Internal Medicine, Family Medicine, Rheumatology, or a related specialty
- •No prior Principal Investigator or clinical research experience required
- •Strong interest in clinical research and patient care
- •Ability to meet required on-site time commitments
Benefits
Responsibilities
- •Serve as Principal Investigator on assigned clinical trials in compliance with ICH-GCP, FDA regulations, and sponsor protocols
- •Oversee study conduct, subject safety, and data integrity
- •Ensure protocol adherence and regulatory compliance
- •Collaborate with Sub-Investigators, Study Coordinators, and research staff
- •Participate in sponsor, CRO, and monitor visits as required
- •Maintain accurate and complete regulatory documentation