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Principal Investigator
2 months ago
Principal Investigator (MD/DO)
The Principal Investigator will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes.
Responsibilities
- Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies.
- Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site.
- Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
- Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
- Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies.
- Ensures and protects the welfare and safety of participants through ethical conduct.
- Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
- Exercises meticulous attention to detail in documentation and patient care.
Requirements
- Medical license (MD, DO) - New Jersey
- 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator)
- Bilingual Spanish a plus
Flexible hours - schedule can be tailored as required.
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