Clinical Research Supervisor (Oncology) Position Available In Orange, Florida
Tallo's Job Summary: The Clinical Research Supervisor in Oncology oversees industry-sponsored and investigator-initiated clinical trials, ensuring compliance with protocols and regulations. Responsibilities include supervising the team, coordinating studies, and providing guidance and training. Requirements include a Bachelor's degree in Healthcare Administration, 2 years of clinical research experience, and proficiency in project management.
Job Description
The Clinical Research Supervisor plays a crucial role in overseeing the conduct of industry-sponsored and investigator-initiated clinical trials. This position ensures compliance with trial protocols, FDA regulations, and ICH/GCP guidelines. They may function as a clinical study coordinator when needed and is responsible for training, mentoring, and developing the clinical study coordinators and research staff across various locations. The role involves close collaboration with managers and leaders to facilitate the initiation and completion of clinical research studies. Responsibilities Supervise day-to-day activities of the clinical research team, ensuring productivity and maintaining staffing schedules. Ensure safe care delivery while respecting the dignity and rights of all patients and participants. Act as a service line expert and resource for the research team, addressing operational barriers. Monitor and evaluate the quality and safety of clinical operations in the assigned area. Build and maintain supportive relationships with team members through regular interactions. Collaborate with operations managers, study intake, and external partners for a smooth transition of study coordination. Develop and maintain Standard Operating Procedures and Work Instructions as directed by the Clinical Research Operations Manager. Provide guidance, education, specialized training, and mentorship to promote team member growth. Coordinate clinical research studies, including planning, organizing, and managing all related activities. Support the preceptorship of new team members, monitoring their progress and maintaining open communication with the Operational Manager. Essential Skills Experience in clinical research, particularly in oncology. Proficiency in project management and clinical study coordination. Knowledge of clinical trials and CRC (Clinical Research Coordinator) responsibilities. Additional Skills & Qualifications Bachelor’s Degree in Healthcare Administration, Research, or related field with 2 years of experience in clinical research or an Associate’s degree with 4 years of experience. Basic Life Support (BLS) Certification.
