Medix™ · 3 weeks ago
Principal Investigator (MD/DO) Clinical Research - 245752
Medix™ is a multi-site clinical research organization specializing in Phase I–IV clinical trials across various therapeutic areas. The Principal Investigator is responsible for the overall conduct and oversight of clinical trials, ensuring subject safety, data integrity, and regulatory compliance while collaborating with clinical research staff and sponsors.
Responsibilities
Serve as Principal Investigator for assigned clinical trials throughout the study lifecycle
Ensure compliance with study protocols, GCP/ICH guidelines, FDA regulations, and institutional policies
Maintain active medical licensure and applicable board certification
Demonstrate thorough understanding of study protocols and target patient populations
Evaluate and ensure subject eligibility based on inclusion/exclusion criteria
Perform medical assessments and evaluations required by the protocol
Oversee informed consent process to ensure ethical and regulatory standards are met
Monitor subject safety, assess adverse events, and ensure appropriate reporting
Collaborate with Medical Director and site leadership on study oversight and medical decisions
Provide training, delegation, and ongoing oversight of clinical research staff
Ensure adequate recruitment planning and feasibility for assigned trials
Conduct protocol-required testing, rating scales, and documentation (paper and electronic)
Attend investigator meetings, sponsor trainings, and educational sessions as required
Support budgetary input and study feasibility assessments as needed
Fulfill all responsibilities outlined on the FDA Form 1572 (or equivalent Statement of Investigator)
Qualification
Required
M.D. or D.O. required
Active, unrestricted medical license in the New Jersey (or ability to obtain)
Board Certified or Board Eligible (Psychiatry, Internal Medicine, Family Medicine, or Emergency Medicine)
Active DEA license (or ability to obtain)
Prior clinical research experience highly preferred (PI or Sub-Investigator experience a plus, but not required)
Strong knowledge of GCP/ICH guidelines and clinical trial regulations
Ability to interpret and implement study protocols accurately
Excellent verbal and written communication skills
Strong organizational skills with attention to detail
Ability to work independently while collaborating effectively within a multidisciplinary team
Calm, professional judgment in urgent or emergent clinical situations
Benefits
Malpractice coverage provided
Comprehensive benefits package including health, dental, vision, disability, life insurance, and retirement plan
Company
Medix™
Medix provides workforce solutions to clients and creates opportunity for contract employees.
Funding
Current Stage
Late StageTotal Funding
unknown2022-09-16Acquired
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