This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
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.
#J-18808-Ljbffr
Worksite address
norfolk, VA, 23500, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.