Job Description
XenoSTART, the preclinical division of START is a translational research organization focused on creating relevant preclinical cancer models. Our xenograft models represent each cancer type and disease stage and are established from patients at our domestic and international cancer centers. The XenoSTART Patient-Derived Xenograft (XPDX) platform includes over 2,500 models annotated with each donor patients cancer treatment and outcome data and characterized using IHC, DNA/RNA sequencing, and relevant in vivo drug efficacy.
Our XPDX models are clinically annotated and include patient treatment history and outcome and are characterized through genomic profiling, histologic analysis, and in vivo drug sensitivity to relevant standards of care. These models may be utilized in the following manner:
- In vivo PK/PD and efficacy studies
- In vivo efficacy panel screens (indication or target focused)
- In licensing of models for internal studies
- Custom model development
- Orthotopic and radiotherapy studies
- Ex vivo and organoid studies
We are hiring Biorepository Research Assistant at our XenoSTART location in San Antonio, TX. This role role is responsible for the organization and management of aspects related to biorepositories housed at XenoSTART including clinical and nonclinical samples and associated data sent to and generated by XenoSTART and collaborators. This position is responsible for documentation and preparation of samples for shipment and for direct interactions with third party providers that process, test and/or characterize samples and management of deliverables and other responsibilities as needed in day-to-day operations.
Essential Responsibilities - Organize and manage clinical and nonclinical samples generated by or sent to XenoSTART; this includes but is not restricted to fresh, frozen, and fixed paraffin-embedded samples.
- Maintain and update XenoSTART models list, IHC and characterization results, and data results as needed for internal studies.
- Compile patient, model and other data related to past, current or future biobank samples, models and other data as needed.
- Assist in organization, documentation, and preparation for internal and sponsor sample shipments including application, submission, and upkeep of all pertinent documentation.
- Interact with pathology group regarding FFPE, IHC, TMA prep, slides, photos, OCT, antibodies, and other tasks as needed.
- Prepare and ship environmental monitoring and pathogen testing samples.
Education & Experience - Bachelors degree in a natural science preferred
- Knowledge of oncology preclinical research preferred
- Must be proficient with Microsoft Office applications; experienced in Excel
- Good record keeping and ability to work in a fast-paced team environment a must.
- Must be computer keyboard knowledgeable and literate (typing 45-50 words per minute).
- Must accurately spell and type information onto manual and computer records.
Best-in-Class Benefits and Perks We value our employees time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
- Comprehensive health coverage: Medical, dental, and vision insurance provided
- Robust retirement planning: 401(k) plan available with employer matching
- Financial security: Life and disability insurance for added protection
- Flexible financial options: Health savings and flexible spending accounts offered
- Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
- Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.
More about The START Center for Cancer Research Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access 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 worlds largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at .
Ready to be part of a team changing the future of cancer treatment? 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 basis of race, color, religion, marital status, age, national origin, ancestry, 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.
Job Tags
Local area, Remote job, Worldwide, Flexible hours,