Job Description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population – leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many – by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.

 
START represents the world’s 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. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – the most effective cancer drug in medical history.

We are hiring a motivated Biorepository Research Assistant I who 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, store and manage clinical and nonclinical samples generated by or sent to XenoSTART; this includes but is not restricted to fresh, frozen, slides and fixed paraffin-embedded samples. Monthly updates of logs for samples and associated consents, collections, and model statues to include capacity/inventory updates.
• Maintain and update XenoSTART models list, IHC and characterization results, and data results as needed for internal studies.
• Compile 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.
• Selecting, pulling and fulfilling sample requests for models that are included in agreements/ projects such as MTA/MTAS, per availability of said selections or alternate selections .
• Select and pull samples as needed for In Vivo Research Assistants and Collaborations.
• Communications between external vendors and internal departments for all requests, issues and concerns relating to agreements, projects or workorder and related requests where applicable.

Education & Experience

• High school diploma/GED.
• Must be proficient with Microsoft Office applications.
• Good record keeping and ability to work in a fast-paced team environment.
• Must be computer keyboard knowledgeable and literate (typing 45-50 words per minute).
• Must accurately spell and type information onto manual and computer records.

Preferred Education and Experience:

• Bachelor’s degree.
• Knowledge of oncology preclinical research.

Physical and Travel Requirements:

• Ability to stand for extended periods of time.
• Ability to perform daily tasks requiring fine motor skills.
• Ability to utilize full range of motion (reaching, bending, etc.).
• Ability to lift 40 pounds.

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 world’s 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  STARTresearch.com .

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

Full time, Work at office, Local area, Worldwide, Flexible hours,

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