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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!
At St. Jude Children’s Research Hospital, we know what can be achieved when the brightest minds face the fewest barriers. That’s why we provide world-class facilities, state-of-the-art technologies, and extraordinary support to ensure scientific and clinical progress is never halted from a lack of resources. You will be part of a collaborative environment where you can see, firsthand, the rewards of your hard work.
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 or Clinical Research Associate- RN I to join our team.
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.
The role of Clinical Research Quality Compliance Analyst (CRQCA) (CRQ) will consist of promoting Clinical Research Quality Management and Education by ensuring adherence to local, state, and federal regulations, and institutional policies and procedures for the responsible conduct of research and providing the day to day management and support of the operations of the Internal Monitoring Committee (IMC).The Analyst is responsible for:
- Preparation of meeting agendas, drafts of meeting proceedings, official IMC memoranda and provides other support for the committee.
- Ensures that the IMC files and database are complete and appropriately maintained to assure appropriate oversight and protections for human subjects.
- Performs Quality Assurance reviews of IMC Reports prior to Agenda assignment to discern unusual or inconsistent documentation, to ensure compliance of research and research related administrative activities of St. Jude studies.
- Performs quality assurance reviews/audits of clinical research practices and processes.
- May also advise on educational offerings based on trends.
St. Jude is anticipating the need for a Clinical Research Scientist in the department of Epidemiology and Cancer Control. This position offers you the opportunity to coordinate the largest cancer survivorship studyin North America. As a Clinical Research Scientist, you will lead a team in their daily activities to support participant recruitment, data collection, protocol implementation and quality assurance. We are looking for someone who can work autonomously, be a servant leader, and look for ways to continuously improve the study management process.
The Clinical Research Associate III acts as a project manager for institutional as well as St. Jude sponsored, multi-center trials, including regulatory, financial, and administrative aspects of the study. This person will also act as site study coordinator for complex, large multi-site and/or multidisciplinary clinical trials. Much of the work will be project based while new studies are coming down the pipeline. This opportunity is an exciting part of our growth, allowing you to work directly with collaborating sites and the faculty sponsor. If you are ready to join our team, then apply now!*This is a grant funded position*
St. Jude is anticipating the need to hire a Manager - Clinical Research Operations in the coming months. As a Manager - Clinical Research Operations team, you provide overall coordination of personnel and research efforts for key projects in the Epidemiology and Cancer Control department including the largest survivorship studyin North America. Entering this role, you are expected to establish relationships with key stakeholders and evaluate the efficiency of current processes. This job exists in a highly visible, highly productive, and fast-paced environment with passionate clinicians and researchers. Some primary responsibilities are as follows:
- Supervise staff and ensure they are equipped to do their job
- Assist with the development of new protocols
- Coordinate the implementation of multiple concurrent survivorship-based research projects
- Oversee participation of collaborating sites
- Provide progress reports for grants and external regulatory agencies or sponsors
- Actively participate in institutional implementation of new clinical trials management and electronic data capture systems
This role is a balancing act to keep complex processes running with minimal interruption, yet we provide you the resources necessary to do your job well. The ideal candidate will learn the challenges of each study assigned to their direct reports and be involved with developing solutions. Take the first step to join our team by applying now!
At St. Jude Children’s Research Hospital, science matters. Our mission is to advance cures, and means of prevention, for pediatric catastrophic diseases through research and treatment. Every one of our professionals shares our commitment to make a difference in the lives of the children we serve.
The Clinical Research Scientist focuses on one or more specific scientific endeavors of clinically-based research as directed by the principal investigator. This position utilizes unique, advanced skills in clinical/population-based methodology to achieve the highest research goals. In this role, you will develop and/or implement research procedures and publish research results. You will also be responsible for initiating and conducting independent research without direct supervision along with assisting with the management of large, multidisciplinary research operations.
We are looking for talented and motivated individuals to fill the position of Clinical Research Scientist. Top candidates are expected to have completed PhD or equivalent doctoral degree, in a related scientific area. Candidates who have a background in social science, public health, epidemiology, and in hospital/medical research, skills in analytical and computational techniques, and excellent written and spoken communication are additional preferred skills. Candidates with demonstration of peer-reviewed journal publications, patents and conference presentations, regulatory experience, and study design are preferred.
The Clinical Research Associate III operates independently with limited supervision and performs activities consistent with those of a study coordinator role. This position also performs data abstraction, collection, and entry to support clinical research and prepares submission for all reportable events, modifications and continuing reviews. 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!
As a Clinical Research Associate-RN III reporting to the Director of the Division of Anesthesiology, you will provide support to our faculty-initiated studies. When a faculty member has new project ideas, you are there to assist with research and proposals while also attending stakeholder meetings. Research has been focused on pain management, yet the scope of projects is about to expand with your help. Other responsibilities include enrolling and educating participants on active studies, updating databases, reviewing research findings, and developing patient safety initiatives. You will enjoy this job if you have a passion for quality and safety as well as a desire to drive studies forward in the clinical research arena. Take the first step to join our team by applying now!
The goal of the Department of Infectious Diseases at St. Jude Children’s Research Hospital is to study devastating diseases of childhood through a comprehensive approach including basic science research, translational trials, and bedside care, and we’re seeking a strategic thought partner and leader to help guide the trajectory of our HIV prevention and treatment program as we grow.
Here at St. Jude, our mission is at the center of all we do, and we’re honored to lead HIV prevention and treatment research for children and youth on a national stage: managing a multimillion-dollar, grant-funded portfolio, designing and implementing ground-breaking new protocols, and leading high-profile clinical trials. In this unique role, you’ll lead a tight-knit, high-performing team of clinical research associates, managing the ebb and flow of cases and protocols while collaborating across departments to drive our mission forward.
St. Jude is leading the way the world understands, treats and defeats childhood cancer and other potentially life-threatening diseases such as HIV infection, and we encourage applicants whose aspirations match the caliber of our work. If you're passionate about research, thrive in collaborative environments, and are a strategic leader with a heart for bold, mission-driven work, we’d love to have you apply.
As a Clinical Research Associate II you will be responsible for the following:
- Operates under general supervision
- Performs activities consistent with those of a Study Coordinator role such as maintenance of protocol portfolio(s), informed consent(s), and preparation/submission of complex study documents
- 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 complex data reports. Serves as a mentor and preceptor to staff