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) - Pennsylvania
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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Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Other, Information Technology, and Management
Industries
Internet Publishing
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