Principal Investigator (Physician) at ALLIANCE CLINICAL LLC – Houston, Texas

About Company:

We’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research, diligent patient care and strong executive management. Our hands-on management team and medical staff are committed to rapid, efficient trials that bring life-changing drugs to market faster; our research staff brings years and years of “in the trenches” experience conducting Phase 1-4 clinical studies. And each one is dedicated to curing disease and improving individual quality of life.

MISSION STATEMENT

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.

About the Role:

The Principal Investigator (Physician) will lead and oversee clinical research projects aimed at advancing medical knowledge and improving patient care within the healthcare and social assistance sector. This part-time role involves designing, implementing, and managing clinical trials and studies, ensuring compliance with regulatory standards and ethical guidelines. The Principal Investigator will collaborate with multidisciplinary teams, including research staff, healthcare professionals, and external partners, to drive scientific innovation and translate research findings into clinical practice. They will be responsible for securing funding, managing budgets, and disseminating research outcomes through publications and presentations. Ultimately, this position plays a critical role in shaping the future of healthcare by contributing to evidence-based medicine and improving health outcomes for diverse patient populations across the United States.

Minimum Qualifications:

• Medical degree (MD or DO) from an accredited institution.
• Board certification in a relevant medical specialty.
• Active and unrestricted medical license to practice in the United States.
• Demonstrated experience in clinical research, including protocol development and clinical trial management.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.

Preferred Qualifications:

• Advanced degree or training in clinical research, public health, or related fields (e.g., MPH, PhD).
• Experience leading multi-center clinical trials or large-scale research projects.
• Proven track record of successful grant writing and securing research funding.
• Familiarity with electronic data capture systems and clinical trial management software.
• Publication history in peer-reviewed medical or scientific journals.

Responsibilities:

• Design and develop clinical research protocols and study plans in accordance with regulatory and ethical standards.
• Lead and coordinate multidisciplinary research teams to ensure effective execution of clinical trials and studies.
• Oversee patient recruitment, informed consent processes, and data collection to maintain study integrity and compliance.
• Manage budgets, secure funding through grant applications, and ensure efficient resource allocation for research projects.
• Analyze and interpret research data, prepare scientific reports, and present findings at conferences and in peer-reviewed journals.
• Ensure adherence to all applicable laws, regulations, and institutional policies governing clinical research.
• Collaborate with institutional review boards (IRBs), sponsors, and regulatory agencies to facilitate study approvals and monitoring.

Skills:

The Principal Investigator will utilize their clinical expertise and research skills daily to design scientifically rigorous studies that address critical healthcare questions. Strong leadership and communication skills are essential for managing research teams, coordinating with stakeholders, and effectively disseminating findings. Analytical skills are applied to interpret complex data sets and ensure accurate reporting of results. Knowledge of regulatory frameworks and ethical standards guides compliance and patient safety throughout the research process. Additionally, grant writing and project management skills support the sustainability and success of ongoing and future research initiatives.