Genitourinary Physician Investigator/Director

The START Center for Cancer Research; Norfolk (VA); On-site; USD 200,000 - 300,000; Full time

Job summary

The START Center for Cancer Research is seeking a Genitourinary (GU) Physician Investigator in Norfolk, Virginia. This physician-scientist role involves leading GU Oncology clinical trials, managing protocols, and ensuring compliance with regulatory requirements. Candidates should have an M.D. and be Board Certified in Medical Oncology or Urology, with a strong background in clinical trials and drug development. Excellent communication and leadership skills are essential. Opportunities for patient engagement and team collaboration are emphasized.

Qualifications

• M.D. or equivalent required.
• Board Certified in Medical Oncology or Urology.
• Clinical trials experience with a strong interest in drug development.

Responsibilities

• Oversee GU clinical trials providing medical direction.
• Collaborate with healthcare providers across disciplines.
• Ensure safety and accuracy of trial data.

Skills

Leadership skills

Clinical trials experience

Understanding of GCP principles

Ability to analyze clinical data

Excellent communication skills

Education

M.D. or equivalent

Board Certified in Medical Oncology or Urology

Job description

We are seeking a Genitourinary (GU) Physician Investigator (PI).

The Genitourinary (GU) Physician Investigator (PI) is a physician-scientist with demonstrated clinical research team leadership skills responsible for the overall preparation, conduct, and management of GU Oncology clinical trials including Phase 1 studies. This role will manage the development and execution of clinical trial protocols, contribute to data analysis, and maintain strong communication and alignment with industry sponsors while maintaining compliance with all regulatory requirements and institutional policies.

Essential Responsibilities

• Strong leadership skills to oversee early and late phase GU clinical trials by providing overarching medical direction and comprehensive medical reviews of protocols in conformance with the investigational plan and good clinical practice
• Work collaboratively across healthcare provider disciplines with urologic oncologists, radiation oncologists, nuclear medicine radiologists, pathologists and medical oncology physicians
• Provide medical and scientific feasibility of all new sponsor inquiries driving growth through strategic partnerships
• Lead and manage a matrix team responsible for the conduct of GU oncology trials
• Ensure the safety and well-being of all trial site participants are protected
• Ensure data collected at the study site is credible and accurate
• Ensure the ethical rights, integrity, and confidentiality of all participants at the trial site are protected
• Develop professional working relationships with sponsors and clinical research organizations involved in study conduct
• Provide expert guidance and support to clinical operations research staff and sponsor client
• Lead continuous quality improvement efforts for clinical research services, integrating best practices and fostering a culture of research excellence and multidisciplinary collaboration
• Develop and implement strategies to enhance patient recruitment and retention in clinical trials
• Strong collaborative skills working with START co-investigator physicians and across the START network

Required Education and Experience

• M.D. or equivalent
• Board Certified in Medical Oncology or Urology
• Qualified for relevant U.S. state medical licensing
• Clinical trials experience with a strong interest in drug development and publications
• Ability to critically analyze clinical scientific data and literature
• Understanding of Good Clinical Practice (GCP) principles, safety and adverse event reporting, FDA regulations, and biomedical research ethics
• Passion for providing excellence of clinical care and for working in a collaborative/ team-oriented environment
• Strong leadership skills with an entrepreneurial mindset encompassing an aggressive approach to growth and expansion

Preferred Education and Experience

• Previous experience with industry-sponsored clinical trials
• Excellent communication skills, with experience in publishing and presenting at scientific meetings
• Translational research experience and familiarity with early and late stage clinical trials

Travel Requirements

• Travel expectations of at least 15% of time

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.