Jobs at Study Hotels

The Clinical Trial Support Assistant role is an onsite, full-time position based in Indianapolis, IN, providing operational support to teams managing investigation materials and clinical supply workflows. Key responsibilities include inputting and updating study supply data with high accuracy, reviewing and organizing material-related documents, tracking communications, and generating reports to monitor study activity. The position also involves maintaining electronic records, assisting with study closeout tasks, and supporting system troubleshooting. This role appeals to detail-oriented professionals seeking to develop expertise in clinical supply systems within a collaborative environment. The company offers comprehensive benefits including medical, dental, vision, paid time off, and a 401(k) plan with employer matching. The work arrangement requires on-site presence during standard business hours with occasional overtime.

The Family Planning Research Assistant 1 role supports clinical and translational research projects within Yale's Division of Family Planning in the Department of Obstetrics, Gynecology, and Reproductive Sciences. Key responsibilities include recruiting study participants, obtaining informed consent, collecting physical measurements and biospecimens, and managing research data with strict adherence to ethical guidelines. The position offers a collaborative environment where the assistant works alongside principal investigators and trainees to advance reproductive health science. This opportunity is appealing for individuals seeking to develop expertise in clinical trials and data analysis while contributing to meaningful medical research. The role operates on a hybrid work model and requires a strong work ethic with the ability to perform self-directed tasks.

This senior principal pathologist role within AbbVie's research and development team focuses on assessing the safety of experimental compounds and devices through the evaluation of animal body fluids and tissues. Key responsibilities include designing and directing toxicology studies, interpreting complex pathological data from necropsy and microscopy, and preparing comprehensive reports for regulatory submissions. The position also involves providing scientific consultation to other departments and leading multidisciplinary teams to identify potential toxicities early in the drug discovery process. The role is appealing for its opportunity to serve as a critical safety representative in advancing new therapies, offering significant professional growth and the chance to work within a collaborative, science-driven environment.

The Clinical Trial Assistant role supports the execution of clinical studies within Scout Clinical, a leader in patient reimbursement and trial logistics. This position collaborates closely with project management teams to ensure operational excellence throughout the study lifecycle. Key responsibilities include coordinating study activities, maintaining project calendars, managing documentation, and configuring user access within the company portal. The role also involves handling client communications, processing invoices, and distributing virtual payments. The position appeals to candidates seeking a fast-paced environment with a culture focused on innovation and making complex processes easier. It offers opportunities for professional growth within a rapidly expanding team and requires strong organizational skills and attention to detail.

This post-doctoral research role is based in the Laboratory of Kathleen M. Caron within the Department of Cell Biology & Physiology at the University of North Carolina at Chapel Hill. The position focuses on investigating G protein-coupled receptor interactions with receptor activity modifying proteins using in vitro biochemical and pharmacological methods. Key responsibilities include characterizing novel receptors in native cells, elucidating receptor mechanisms, and identifying new interacting partners. The role appeals to candidates seeking a collaborative environment within the Research Triangle, offering access to resources at nearby Duke and NC State universities. The position provides exceptional career development opportunities through the university's Office of Postdoctoral Affairs and is situated in a region consistently rated for high quality of life and biotechnology growth.

This full-time Senior Clinical Research Associate role focuses on oncology clinical trials within a Fast-paced FSP team based in Northern California. The position involves managing all aspects of site monitoring, including pre-study visits, routine oversight, and close-out procedures to ensure protocol adherence and patient safety. Key responsibilities include verifying informed consent, reviewing data integrity on Case Report Forms, managing Serious Adverse Event reporting, and coordinating with vendors and study staff. The role appeals to candidates seeking a dynamic environment where adaptability and teamwork are essential for success. While the position is designated as remote, it requires significant travel, estimated at 40-50% of the time, to visit clinical sites across the region.

This Research Fellow position supports the dermatology department in advancing clinical trials and investigator-initiated studies. The role involves assisting with patient enrollment, protocol development, IRB documentation, and data collection for sub-specialty clinics such as contact dermatitis and immunobullous diseases. Key responsibilities include presenting research findings to faculty and leadership, contributing to publications, and analyzing data related to various skin disorders. The position is ideal for an MD or DO candidate with strong analytical abilities and a passion for dermatological research. It offers a collaborative environment to work closely with faculty and residents while developing expertise in clinical research methodologies and patient recruitment.

This post-doctoral research associate role is based at the Center for Animal MRI within the University of North Carolina at Chapel Hill, affiliated with the Biomedical Research Imaging Center and the Department of Neurology. The position focuses on developing and applying novel functional magnetic resonance imaging techniques, specifically enhancing zero echo time and ultra-short echo time methods to map brain function during active behaviors. Key responsibilities include designing MRI protocols, acquiring and analyzing complex imaging data, and potentially editing MRI sequences on Bruker platforms. The role offers the opportunity to work with cutting-edge neuromodulation and recording technologies in a collaborative academic environment dedicated to advancing silent and artifact-resistant imaging capabilities for neuroscience research.

This full-time teacher role focuses on exceptional education within a school district, aiming to foster student development into mature and responsible individuals. The position involves planning individualized study programs, employing diverse instructional techniques to meet unique student needs, and maintaining accurate records of student progress. Key responsibilities include creating a supportive classroom environment, supervising teacher aides, and implementing district literacy initiatives. The role offers a collaborative professional setting with opportunities for continuous growth and committee participation. The position is based on-site for 190 days per year and requires appropriate teaching credentials and a degree in the relevant field.

This full-time Grade 4 teaching position for the 2025-2026 school year focuses on fostering student development into responsible individuals through a structured curriculum. The role involves planning engaging lessons tailored to diverse student needs, implementing the district's CORE Literacy initiative, and maintaining a positive, safe classroom environment. Key responsibilities include assessing student progress, managing classroom behavior, and collaborating with staff and parents to support learning goals. The position offers the opportunity to work within a supportive educational community that values professional growth and student well-being. The role is based on-site for 190 days per year.

The Senior Director, Clinical Science, Alzheimer's Disease role leads the strategic development and delivery of endpoint management and quality assurance for global clinical trials in neurodegenerative disorders. Key responsibilities include defining study scopes, creating data quality strategies, managing rater training programs, and serving as a subject matter expert for scientific communications and publications. The position also involves supporting business development by collaborating with pharmaceutical clients on proposals and consultative sales. This opportunity appeals to professionals seeking to advance brain health science within a virtual-first company that offers remote flexibility, a collaborative culture, and robust professional development resources.

The Biostatistician II role supports clinical research programs by independently leading studies and delivering high-quality statistical analyses. Key responsibilities include developing Statistical Analysis Plans, generating randomization schedules, and creating tables, figures, and listings using SAS. The position requires reviewing protocols, validating programming outputs, and ensuring compliance with regulatory guidelines such as FDA and ICH standards. This opportunity is appealing for professionals seeking to work on Phase 1 trials and early safety endpoints within a collaborative, client-focused environment. The role involves cross-functional teamwork and offers the chance to mentor junior staff while maintaining flexibility in work assignments.

The Clinical Research Assistant role supports the Endocrinology, Diabetes and Metabolism department within the Medicine division at The Ohio State University. Key responsibilities include managing participant recruitment and retention, conducting phone screenings and study visits, obtaining informed consent, and utilizing platforms like RedCap and IRB systems for data management. The position offers a stable full-time schedule with a focus on advancing medical research in a specialized field. This opportunity is appealing for individuals seeking to contribute to meaningful health studies within a collaborative academic medical center environment.

This full-time Clinical Research Coordinator role supports Phase I through IV trials within CenExel's specialized research centers, focusing on areas such as psychiatry, dermatology, and neurology. The position involves coordinating patient involvement from study initiation to completion, organizing research data, and ensuring strict adherence to ICH and GCP regulations. Key duties include observing subjects, performing safety assessments like vital signs and blood draws, reporting adverse events, and assisting with protocol development and staff training. The role offers a collaborative work environment that emphasizes teamwork, positive leadership, and work-life balance, with opportunities for professional growth in a respected facility. The position is based on-site in an office setting with a standard Monday through Friday schedule, though occasional overnight travel for training may be required.

This full-time Research Assistant role supports the mission of Pregnancy Justice by documenting pregnancy-related criminalization across the United States. Reporting to the Senior Research Manager, the position involves identifying relevant legal cases, collecting and coding data for a major interdisciplinary study, and assisting with data visualization and report creation. The role requires maintaining strict confidentiality and collaborating with a team of scholars and advocates. The position offers a hybrid work arrangement with two days required in the New York City office and provides the opportunity to contribute to impactful human rights research. The organization fosters a collaborative, inclusive culture with flexible Friday schedules and a commitment to professional growth within a unionized environment.

The Associate Director, Preclinical Partnerships role at IAVI leads the oversight and execution of R&D studies within the Vaccine Design and Development Laboratory in Brooklyn. Key responsibilities include managing sub-awardees and external partners, directing study design and data analysis, and supporting grant proposals and fundraising strategies to advance vaccine candidates. This position appeals to candidates seeking to translate scientific discoveries into global public health impact by fostering unique collaborations across academia, industry, and governments. The role offers the opportunity to work on critical missions addressing HIV and tuberculosis while contributing to a culture of innovation, integrity, and global teamwork.

This full-time special education teaching role is based at Thomas Jefferson High School within the Arlington Public Schools system. The position focuses on supporting students with high-functioning Autism Spectrum Disorder and Asperger's Syndrome through direct instruction in social skills, study habits, and organizational strategies. Key responsibilities include designing and evaluating individual behavior management plans, co-teaching with general education staff, and leading lessons in both small and large group settings. The role requires Virginia licensure and certification in Special Education. The position offers the opportunity to work within a supportive educational environment that values inclusive practices and collaboration. The job is located on-site at the school.

This full-time elementary teaching role is based at Rashkis Elementary School within the Chapel Hill-Carrboro City Schools district. The position focuses on delivering Spanish language instruction to students using the North Carolina Standard Course of Study. Key responsibilities include developing engaging lesson plans, adapting curriculum for diverse learning needs, managing classroom behavior, and communicating regularly with parents and staff. The role offers the opportunity to foster a supportive learning environment that encourages student growth and cultural appreciation. The position is scheduled for ten months and requires a valid North Carolina teaching license and a bachelor's degree.

This Specified Term role within the Pediatric Oncology Research Team at the University of Iowa supports the planning and execution of clinical studies for children with cancer. Key responsibilities include coordinating patient recruitment and visits, managing data entry and electronic databases to ensure regulatory compliance, and handling laboratory specimen processing. The position also involves liaising with external hospitals and preparing documentation for sponsor monitoring. The role appeals to candidates seeking to contribute to a national leader in pediatric medicine and cutting-edge cancer research. It offers a hybrid work arrangement combining on-campus and remote duties within Iowa, providing a collaborative environment focused on advancing treatments for childhood illnesses.

The Clinical Research Coordinator role at Huntsman Cancer Institute supports the Principal Investigator in managing the implementation and quality control of cancer research studies across the Intermountain West region. Key responsibilities include ensuring regulatory compliance with FDA and IRB guidelines, managing study budgets and participant enrollment, and coordinating all aspects of patient interactions from screening to informed consent. The position also involves supervising junior staff and maintaining detailed research documentation. This opportunity appeals to professionals seeking to contribute to a mission-driven organization dedicated to reducing the global cancer burden. The role offers a collaborative environment with opportunities for professional growth, requiring a blend of administrative precision and patient-centered care within a hybrid work setting.

This full-time Clinical Trials Assistant role supports the Shockwave Reducer project within Johnson & Johnson's R&D Operations team in New Brighton, Minnesota. The position involves managing study payments and invoice processing, coordinating the shipment of clinical study supplies, and maintaining the Trial Master File to ensure regulatory compliance. Key responsibilities also include handling project communications, updating clinical databases, and assisting with meeting logistics. The role offers the opportunity to contribute to innovative cardiovascular treatments while working in a fast-paced, inclusive environment that values professional growth and collaboration.

The Clinical Trial Associate role at Crinetics supports the development of therapies for endocrine diseases within a patient-centric, team-oriented culture. Key responsibilities include executing study activities according to protocols, managing regulatory documents and Trial Master Files, and coordinating study start-up, conduct, and closeout phases. The position requires collaboration with cross-functional teams and external vendors to ensure high-quality outcomes and compliance with Good Clinical Practice guidelines. This opportunity appeals to candidates seeking to contribute to meaningful medical innovation in an inclusive, dog-friendly environment. The role is based in San Diego with minimal travel requirements of up to 5%.