Principal Investigator Overview • The Principal Investigator oversees clinical trial activities, ensuring adherence to FDA, ICH, GCP, and HIPAA guidelines. • Collaborates with local and central teams to enhance clinical oversight and study quality at the site. • Evaluates participant eligibility, ensuring safe and ethical trial execution. • Provides leadership to ensure compliance with protocols and regulatory standards. • Engages in participant recruitment, retention, and successful study delivery. • Participates in training sessions and investigator meetings to maintain current knowledge. • Handles sensitive information confidentially, adhering to HIPAA guidelines. • Supports the team with protocol training and operational efficiency improvements. Principal Investigator Key Responsibilities & Duties • Ensure participant safety and ethical conduct of clinical trials. • Lead site operations, focusing on efficiency and regulatory compliance. • Evaluate participant eligibility and oversee enrollment processes. • Collaborate with sponsors, clients, and team members for trial success. • Maintain accurate records and adhere to protocol guidelines. • Conduct staff training on protocols and procedures. • Participate in investigator meetings and continuing education activities. • Adapt to workload changes and prioritize tasks effectively. Principal Investigator Job Requirements • Doctor of Medicine (MD) degree and active physician license in good standing. • Minimum of 2 years of experience; 3 years preferred. • Board certification in area of specialty required. • Proficiency with MS Office, EHR systems, and web applications. • Strong organizational skills, attention to detail, and communication abilities. • Bilingual proficiency in English and Spanish highly preferred. • CPR certification required; ACLS preferred. • Ability to handle sensitive information confidentially and professionally.