Job Title: Principal Investigator (PI) Family/Internal Medicine

Location: Homestead, FL

Position Overview:

CRO Strategies is seeking an experienced and dedicated Principal Investigator (PI) specializing in Family or Internal Medicine to join our Homestead site. The PI will play a crucial role in leading and overseeing clinical research studies, ensuring they are conducted in accordance with all regulatory requirements and high ethical standards. This role demands a seasoned professional with a strong background in clinical trials, patient care, and a commitment to advancing medical research.

Key Responsibilities:

• Lead and manage clinical research studies from inception to completion, ensuring compliance with all regulatory and ethical guidelines.
• Oversee patient recruitment, enrollment, and retention, ensuring the safety and well-being of study participants.
• Collaborate with cross-functional teams, including research coordinators, sub-investigators, and administrative staff, to ensure smooth and efficient study operations.
• Develop and implement study protocols, informed consent documents, and other essential study documentation.
• Monitor and report on study progress, including data collection, adverse events, and study outcomes.
• Maintain accurate and complete study records in accordance with Good Clinical Practice (GCP) and other relevant guidelines.
• Communicate effectively with sponsors, regulatory agencies, and institutional review boards (IRBs).
• Stay current with developments in the field of Family/Internal Medicine and clinical research methodologies.

Qualifications:

• Medical degree (MD or DO) with board certification in Family Medicine or Internal Medicine.
• Minimum of 5 years of experience as a Principal Investigator or Sub-Investigator in clinical research.
• Strong knowledge of GCP, FDA regulations, and other relevant regulatory requirements.
• Proven track record of successfully conducting clinical trials and managing research teams.
• Excellent interpersonal and communication skills, with the ability to engage and motivate study participants and staff.
• Strong organizational skills and attention to detail.
• Ability to work collaboratively in a fast-paced, dynamic research environment.

Preferred Qualifications:

• Experience in conducting Phase I-IV clinical trials.
• Additional certifications in clinical research (e.g., CCRP, CCRC) are a plus.
• Bilingual proficiency in English and Spanish.