The START Center for Cancer Research · 4 days ago
Director, Clinical Research / Genitourinary (GU) Clinical Investigator
Myrtle Beach, SC
Full-time
Onsite
Director/ExecutiveThe START Center for Cancer Research is the world’s largest early phase site network dedicated to oncology clinical research. The Director, Clinical Research / Genitourinary (GU) Clinical Investigator is responsible for the overall preparation, conduct, and management of GU Oncology clinical trials, ensuring compliance with regulatory requirements and maintaining strong communication with industry sponsors.
BiotechnologyHealth CareLife ScienceMedicalOncologyPharmaceutical
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
Qualification
Required
M.D. or equivalent
Board Certified in Medical Oncology or Urology
Qualified for relevant US 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 entrepreneurial mindset encompassing an aggressive approach to growth and expansion
Preferred
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
Benefits
Comprehensive health coverage: Medical, dental, and vision insurance options provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Company-paid life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Company
The START Center for Cancer Research
The START Center for Cancer Research is a oncology and biotechnology research company.
501-1000 employees
Funding
Current Stage
Late StageLeadership Team
Chris Takimoto
Global Chief Medical Officer
Recent News
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