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 Sr. Clinical Analyst.

This is a remote role. The annual base salary for this role is $100,000 - $125,000 + Bonus. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 

Essential Responsibilities

·       Analyze medical oncology clinical workflows to improve efficiency and patient outcomes.

·       Implement and maintain oncology-specific EHR systems (Aria, OncoEMR).

·       Implement and maintain ancillary systems (Cardiology, Radiology, etc).

·       Develop, test, and maintain HL7 interfaces to ensure seamless data exchange between oncology systems.

·       Troubleshoot HL7 messaging issues and optimize interoperability between EHRs and third-party applications.

·       Provide technical support and training to oncologists, nurses, and research teams.

·       Participate in project management for the implementation of new technologies.

·       Conduct audits and quality assurance checks on oncology clinical data systems.

·       Develop reports and dashboards for cancer treatment outcomes and research analytics.

·       Manage tickets to track system enhancements, bug fixes, and workflow optimizations.

·       Work with cross-functional teams to prioritize and resolve reported issues.

·       Conduct user testing and feedback analysis to refine systems functionality

·       Ensure compliance with HIPAA, FDA, and oncology clinical trial regulations.

Education & Experience

·       Bachelor’s or Master’s degree in Health Informatics, Computer science or related field

·       Previous experience in a clinical setting.

·       Previous experience with administration of electronic health records (EHR) systems

·       Experience with HL7 messaging standards, interface engines (e.g., Cloverleaf, Mirth, Ensemble), and interoperability protocols.

·       Strong analytical and problem-solving skills.

·       Excellent communication and interpersonal skills.

·       Experience with data visualization and reporting tools.

·       Knowledge of healthcare regulations and compliance.

·       Proficiency in SQL and other database management tools.

·       Project management experience.

·       Excellent organizational and multitasking abilities.

·       Ability to work collaboratively in a team environment.

·       Attention to detail and high level of accuracy.

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.