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.