Sub-Investigator/Principal Investigator

Overview

• Serve as a Sub-Investigator/Principal Investigator in clinical research, ensuring compliance with protocols and federal regulations.
• Conduct clinical trials with a focus on patient safety and data integrity.
• Collaborate with multidisciplinary teams to oversee trial activities and patient care.
• Perform physical examinations and evaluate patient eligibility for trials.
• Provide guidance and training to clinical staff on trial protocols.
• Maintain accurate documentation and ensure adherence to Good Clinical Practice (GCP).
• Evaluate adverse events and ensure proper reporting and documentation.
• Participate in site visits, training sessions, and monthly staff meetings.
• Support recruitment efforts and patient counseling for clinical trials.

Key Responsibilities & Duties

• Attend site initiation visits and protocol training sessions.
• Perform delegated study tasks under Principal Investigator oversight.
• Conduct informed consent processes and ensure protocol adherence.
• Evaluate patient eligibility and document medical histories.
• Review lab results and assess clinical significance of findings.
• Collaborate with clinical staff to ensure study compliance and data accuracy.
• Address adverse events and drug reactions with thorough documentation.
• Participate in investigator meetings and company events as needed.
• Provide clinical oversight and support for research activities.

Job Requirements

• Doctor of Medicine (MD) degree with active accreditation.
• Minimum of 3 years of experience in clinical research.
• Credentialed with Davita and Fresenius Kidney Centers.
• In-depth knowledge of FDA-GCP regulations and ethical research practices.
• Strong analytical, organizational, and communication skills.
• Ability to work collaboratively in a fast-paced research environment.
• Bilingual proficiency is highly preferred.
• Availability for 10-15 hours per week on-site in Hollywood, FL.
• Commitment to protecting human subjects and ensuring data integrity.