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There’s a reason St. Jude Children’s Research Hospital is consistently ranked on Fortune Magazine’s “100 Best Places to Work For” list. At our world-class pediatric research hospital, every one of our professionals shares our commitment to make a difference in the lives of the children we serve. There’s a unique bond when you are part of a team that gives their all to advance the treatments and cures of pediatric catastrophic diseases. The result is a collaborative, positive environment where everyone, regardless of their role, receives the resources, support, and encouragement to advance and grow their careers and be the force behind the cures.
As a member of the Epidemiology & Cancer Control clinical research team, you will serve as the protocol expert for assigned clinical trials. Our goal is to improve the lives of pediatric cancer survivors through clinical research related to late effects of cancer treatment. Your primary responsibilities will include consenting and enrolling study participants as well as coordinating with other patient care teams throughout the hospital. Great attention to detail, good organization and interpersonal skills are important for this position. Take the first step to join our team by applying now! This is a Grant Funded position.
As a member of the Epidemiology & Cancer Control clinical research team, you will serve as the protocol expert for assigned clinical trials. Our goal is to improve the lives of pediatric cancer survivors through clinical research related to late effects of cancer treatment. Your primary responsibilities will include consenting and enrolling study participants as well as coordinating with other patient care teams throughout the hospital. Clinical Trials and Drug Studies skills are important for this position. Other key skills to possess are attention to detail, organization and interpersonal Take the first step to join our team by applying now!
Overview
There is a reason St. Jude Children’s Research Hospital is consistently ranked on Fortune Magazine’s “100 Best Places to Work For” list. At our world-class pediatric research hospital, every one of our professionals share our commitment to make a difference in the lives of the children we serve. There is a unique bond when you’re part of a team that gives their all to advance the treatments and cures of pediatric catastrophic diseases. The result is a collaborative, positive environment where everyone, regardless of their role, receives the resources, support and encouragement to advance and grow their careers.
About the position
St. Jude is anticipating hiring a Clinical Research Associate I or Clinical Research Associate II who will operate under general supervision and perform activities consistent with those of a Study Coordinator role, namely maintenance of protocol portfolio(s), informed consent(s) and preparation/submission of complex study documents. This position also performs data abstraction, collection, and entry to support clinical research and prepares submission for all reportable events. The selected candidate develops, maintains, and/or monitors case report forms and ensures compliance with prescribed interventions and evaluations of the assigned protocol(s). Provision of data to the collaborating research organization or study sponsor and preparation of complex data reports as well as serving as a mentor and preceptor to staff are also key responsibilities.
About the Department of Radiation Oncology
Known for setting standards in technical delivery of radiotherapy and clinical trials, the Department of Radiation Oncology is a full-service department dedicated to clinical research and treatment of 300 children, adolescents, and young adults each year. With the mission of providing expert and compassionate clinical care, the department is the largest group of experts devoted to pediatric radiation oncology who collectively treat more children than any other cancer center or hospital in the country. The department includes:
- Multidisciplinary team: Pediatric radiation oncologists, physicists, dosimetrists, radiation therapists, registered nurses, nurse practitioners as well as supportive research teams (anesthesia, sedation, social work and child life specialists to name a few).
- World-class resources: This includes the first worldwide installation of detector-based spectral CT and digital PET/CT in a Radiation Oncology Department, state-of-the-art 1.5T and 3T MR scanners (radiotherapy simulators), a dedicated PET/CT and the world’s first proton therapy center with pencil beam scanning technology designated solely for the treatment of pediatric cancer.
- State-of-art facility: The department has 20,000 square feet of clinical space that includes a clinic, treatment planning, therapy, anesthesia and sedation support. There are two linear accelerator systems with image-guidance, a HDR/fluoroscopy suite, and spectral CT and 1.5T MR systems dedicated to treatment planning. The adjacent 25,000 square feet St. Jude Red Frog Events Proton Therapy Center includes two gantry rooms and a fixed beam room; each equipped with high-precision patient positioning, volumetric image-guidance systems, and dedicated scanning nozzles.
About Memphis
This position is based in Memphis, TN; relocation assistance is available. Memphis is a family-friendly metropolitan area that more than a million residents call home. Memphis is recognized for its world-class music, food and hospitality. Cost of living is one of our biggest attractions; in fact, Money listed Memphis as one of the least expensive cities in which to raise a child. Mild winters and beautiful green spaces make the city a magnet for outdoor enthusiasts – there are over 200 miles of bike-friendly lanes with more being added. Forbes recently named Memphis the 4th happiest city in which to work. Why live anywhere else?
Work Schedule:
Monday-Friday 8am-5pm
Take the first step to join our team by applying now!
As a member of the Division of Cancer Survivorship, you will be instrumental in advancing childhood cancer survivorship. Much of your time will be spent working with the task force leaders to coordinate development, updates, and optimization of the Children’s Oncology Group Long-Term Follow-Up Guidelines for Survivors of Childhood, Adolescent, and Young Adult Cancers, which will include communication with and coordination of guideline task force leaders and members across multiple institutions and disciplines, copy-editing guideline revisions, and streamlining guideline processes.
In this role, you will be working with the predominantly utilized childhood cancer survivorship guideline in North America, and among one of the foremost childhood cancer survivorship clinical and research groups in the world. This position will allow you to work with a dynamic and collaborative research team, pushing the boundaries to continue to enhance childhood cancer survivorship guideline development and utilization. Take the first step to join our team by applying now!
As a Clinical Research Associate RN II on this team, you will have the unique opportunity to work to improve the quality-of-life of St. Jude patients. The selected candidate will need be very detailed oriented, organized and be able to perform in-depth data abstraction, collection, and entry to support clinical research. The candidate will also ideally be a skilled communicator, as this role also includes working with patients and families enrolled on quality-of-life studies. We are a hard working team who care deeply about our mission, our research, our St. Jude patients and families, and each other as well.
As a Clinical Research Associate III (Regulatory) in Infectious Diseases, you act as project manager for institutional as well as St. Jude sponsored, multi-center trials, including regulatory, financial, and administrative aspects of the study. For complex, large multi-site and/or multidisciplinary clinical trials, will coordinate all aspects of the study. Responsibilities also include data abstraction, collection, and entry; preparing submissions for all reportable events; maintaining case report forms; and ensuring compliance with prescribed interventions and evaluations of the assigned protocol. You may be asked to prepare reports for various stakeholders on any given study. Take the next step to join our team by applying now!
The Department of Epidemiology and Cancer Control housed at St Jude Children’s Research Hospital in Memphis, Tennessee, is seeking applicants for a full-time mobile Health (mHealth) Research Scientist position for a National Cancer Institute-funded project. The candidate will work with senior faculty members, a project coordinator, Clinical Research Associates, and other researchers to improve health outcomes for aging childhood cancer survivors. The scientist will collaborate with an experienced health informatics/IT team to develop, deploy, and maintain mHealth platforms for collecting patient-reported outcomes and digital health markers for research. Under the supervision of lead faculty members, the candidate will be engaged in a variety of research activities related to conducting literature review, data collection and analysis, creating training materials for patient engagement, writing research papers, engaging in mHealth-enabled health interventions, and grant preparations.
Why St. Jude?Precision therapies. Better vaccines. Healthier, happier survivors. We dream big, and build our research programs to match. The engine of discovery at St. Jude is powered by some of the most reputable minds in science and medicine, equipped with world-class resources and driven by the shared mission of advancing cures. We understand that fundamental science builds the foundation for clinical impact. We are committed to supporting hypothesis-driven and exploratory research that asks daring questions to drive innovation.To support this pursuit, we need a Director of Neuropsychology Research Operations to lead our team. For more on what's happening in neuropsychology and at St. Jude, please watch this lecture by our very own Kevin Krull, PhD, Faculty Member in Epidemiology & Cancer Control.
As a Clinical Research Associate II in the pharmacokinetic (PK) study lab, you are responsible for communicating with collaborating sites to manage shipment of supplies, collection of samples, and obtaining all necessary clinical information. Acting as a study coordinator, you ensure the mandatory PK studies in the brain tumor program are both implemented and performed correctly. The studies are not only growing in complexity, but also they are growing by adding new participating sites. Primary responsibilities include:
- Communicating with study team members about scheduling PK study appointments in the clinic
- Accessioning samples from the clinical lab
- Gathering necessary information about samples and entering data into relevant databases
- Providing data reports to CRO, study sponsors and/or principle investigators
- Develop and monitor PK data collection forms and related documents
Take the first step to join our team by applying now!
The Clinical Research Associate II operates independently with limited supervision. This position also performs data abstraction, collection, and entry to support clinical research and prepares submission for all reportable events. The selected candidate develops, maintains, and/or monitors case report forms and ensures compliance with prescribed interventions and evaluations of the assigned protocol(s). Provision of data to the collaborating research organization or study sponsor and preparation of complex data reports as well as serving as a mentor and preceptor to staff are also key responsibilities. You will learn from some of the best clinicians in the world as part of the Cancer Center Administration clinical research team. The person in this position will also be expected to work with St. Jude sponsored and industry sponsored studies as needed. You will be opening and managing multiple studies while interfacing with a variety of departments. Take the first step to join our team by applying now!
The Clinical Research Associate II operates independently with limited supervision. This position also performs data abstraction, collection, and entry to support clinical research and prepares submission for all reportable events. The selected candidate develops, maintains, and/or monitors case report forms and ensures compliance with prescribed interventions and evaluations of the assigned protocol(s). Provision of data to the collaborating research organization or study sponsor and preparation of complex data reports as well as serving as a mentor and preceptor to staff are also key responsibilities. You will learn from some of the best clinicians in the world as part of the Hospitalist and Bioethics Program clinical research teams. The person in this position will also be expected to work with St. Jude sponsored and industry sponsored studies as needed. You will be opening and managing multiple studies while interfacing with a variety of departments. Take the first step to join our team by applying now!
The St. Jude Comprehensive Cancer Center and the Developmental Biology and the Hematological Malignancies program are excited to announce a new opportunity for a Clinical Project Manager who will report to the Director of Clinical Trials Management, Oncology Programs. You will work with faculty investigators in the Leukemia/Lymphoma Division to develop new St. Jude sponsored clinical trials, expanding the clinical trials portfolio, working with key internal and external stake holders and study related communications. You will collaborates with preclinical project management on assigned translational projects to ensure adequate project coverage on translational projects. You will coordinate with leadership and clinical trial marketing, clinical trial concept development, clinical trial development, and clinical trial start-up activities on assigned St. Jude sponsored clinical trials.
As a Clinical Research Associate on this team, you will have the unique opportunity to work to improve the quality-of-life of St. Jude patients. Currently, we are seeking a Clinical Research Associate - I . The ideal candidate operates under general supervision. Performs data abstraction, collection, and entry to support clinical research. Prepares submission for all reportable events. Develops, maintains, and/or monitors case report forms. Ensures compliance with prescribed interventions and evaluations of the assigned protocol(s). Provides data to the collaborating research organization or study sponsor. Prepares data reports. If you are excited about this role, we look forward to reviewing your application.
Be part of one of the world’s premier research and treatment centers for childhood cancer. As the Clinical Research Associate I, you will review internal and external medical charts, enter abstracted data into research registries, and work with clinical providers to interpret results. These data will be used by researchers at St. Jude and across the world to push cures forward and inform future investigations. St. Jude will act as a leader among both local and national collaborating sites to advance the field of palliative care. You also will spend time in the clinic explaining the study to families, consenting participants, following up with study activities, and participating with the data analysis process. This position presents an exciting challenge of working with patients, families, researchers, and international experts in the fields of pediatric oncology and palliative care.
This is a great opportunity for you to start your career in clinical research, coming in at the beginning of a project. You will have the opportunity to learn how complex collaborations work in the clinical research industry, gaining transferable skills for future growth. Apply now if you are ready to join our team!