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The START Center for Cancer Research (START) is the worlds largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Accesstocutting edgetrials throughout the UnitedStatesand Europe.

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.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 areseekingaClinical Research Budget Analysttoprovide effective development, implementation, and maintenance of START financial guidelines to secureappropriate billingand compliance.The annual base salary for this remote role is $65,000 - $80,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.
Essential Responsibilities:

• Review and interpret clinical trial protocols, proposed budgets, and supporting documents to accurately capture all clinical trial financial activity.

• Utilize coding knowledge for budgeting as needed (CPT, HCPCS).

• Develop and negotiate budgetsofmedium complexityrated initial studies and amendments, perform coverage analysis, and negotiate contract payment terms, andassistwith contract execution in a proactive andtimelymanner.

• Work closely with clinical team and staff to confirm understanding of clinical research protocol,identifystandard of care/ or routine care and research related activities.

• Prepare budget and contract proposals for Quality Control (QC) review prior to presenting documents for negotiation with industry sponsors or clinical research organizations (CROs).

• Assist in specialprojectsassigned by management and perform other related duties as requested.

Required Education and Experience:

• Bachelors degree in financial or businessadministration field(Accounting, Finance, Business Administration, or similar field) or equivalent experience and/or training.
  

• Minimum of three years of budget experience or equal level of education and experience.

• Clinical Trial Management System (CTMS) experience.

• Intermediate to Advanced MS Office Excel and other MS Office programs.

• Experiencein Adobe,DocuSign,FileMakerand other technical platforms.

• Comprehensive critical thinking skills,and attention to detail.

• Strong interpersonal skills with peers,and excellent communication skill

Preferred Education and Experience:

• Experiencein a healthcare or clinical research setting.

• Oncology experience.

• Coding knowledge (CPT, HCPCS).

Physical & TravelRequirements:

• Approximately 80% oftimeis spent sitting.

• Very fast-paced and ever-changing healthcare environment.

• Demanding deadlines andtime frames.

• Frequent use ofcomputer,keyboard, andmouse.
  

Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to yourwell-beingand growth is reflected in a competitive compensation packagebased on experiencealong with comprehensive benefits designed to support you both personally and professionally:

• 401(k) retirement savings plan with employer match

• Eligibility for an annual performance bonus, based on role and company results

• Generous paid time off and paid holidays

• Comprehensive medical, dental, and vision coverageand optional insuranceoptions

• Companypaidlife and disability insurance for added financial protection

• Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one

• Flexible FSA and HSA plans to support your financial wellness

• Commitment to a supportive environment that values balance, wellbeing, and flexibility

• Werecommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,youlljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe worlds largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of Hope Through Access.As an example, in San Antonio, where START was founded, STARTtreated the first patient ever with Keytruda one ofthe most effective cancerdrugsin medical history.

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. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminateon the basis ofrace, 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.