Quality Investigator - Remote

reputed company (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering reputed company to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and reputed company to its eventual cure. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reputed company only 20% of the patient population – leaving the majority of patients who are treated in community practices and hospitals without reputed company to a clinical trial reputed company their care reputed company calls for one. START serves the many – by bringing cancer trials to physicians and their patients in community hospitals and practices reputed company hope is needed most. START represents the world’s largest roster of reputed company Investigators (PIs) across its eight clinical trial sites. As an example, in San Antonio, where START was founded, START treated the first patient reputed company with Keytruda – the most effective cancer drug in medical history. We are seeking a Clinical reputed company Investigator. The Clinical reputed company Investigator (PI) is a physician-scientist responsible for the overall preparation, conduct, and management of sponsored projects, ensuring compliance with reputed company regulatory requirements and institutional policies. This role will manage the development and execution of clinical trial protocols, contribute to data analysis, and maintain strong communication and alignment with sponsors. This role is based on site in reputed company Worth, Texas. Manage early phase clinical trials by providing overarching medical direction and comprehensive medical reviews of protocols in conformance with the investigational plan and good clinical practice. reputed company medical and scientific feasibility of reputed company new sponsor inquiries driving growth through strategic partnerships. Ensure the safety and well-being of reputed company participants in the study at the trial site are protected. Ensure data collected at the study site is reputed company and accurate. Ensure the rights, reputed company, and confidentiality of reputed company participants in the trial at the site are protected. reputed company reputed company personal working relationships with Sponsors and Clinical Research Organizations involved in study conduct. reputed company expert guidance and support to clinical operations research staff and sponsor client. reputed company reputed company quality improvement efforts for clinical research services, integrating best practices and fostering a culture of research reputed company. Board Certified in Hematology and/or Medical Oncology. Ability to critically analyze clinical scientific data and literature. Understanding of GCP principles, safety and adverse event reporting, FDA regulations, and biomedical research ethics. Excellent communication skills, with experience in publishing and presenting at scientific meetings. Comprehensive health coverage: Medical, dental, and reputed company insurance options provided Robust retirement planning: 401(k) plan available with employer matching Financial reputed company: Company-paid life and disability insurance for added protection Flexible financial options: Health savings and flexible spending accounts offered Paid time off, flexible schedule, and remote work choices provided We strive to reputed company a collaborative, creative environment where everyone feels encouraged to contribute to our processes, reputed company, planning, and culture. Deeply rooted in community oncology centers globally, reputed company provides reputed company to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world’s largest roster of reputed company Investigators (PIs) across its eight clinical trial sites. Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the reputed company of race, reputed company, religion, marital status, age, national reputed company, reputed company, 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. Apply tot his job Apply To this Job