Clinical Research Revenue Cycle Specialist - Remote

Job Description

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 Clinical Research Revenue Cycle Specialist. This role can be hybrid or remote, depending on where the candidate lives.

This role will support the Analyst team by training on creating and approving monthly clinical trial Invoices for active studies at assigned domestic or international sites.

The annual base salary for this role is $55,000 - $75,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.

Essential Responsibilities

• Help to review / approve active study reconciliations to ensure all patient visits are priced correctly per the budget
• Work closely with the domestic and international AR Team to ensure sponsor payments are applied correctly

Perform clinical study analysis for profitability and performance

• Work closely with study budget and contracting team to resolve any billing issues with sponsor
• Assist when needed to help research and resolve any Sponsor inquiries
• Ensure month end deadlines are met timely and accurately
• Serve as Team lead for CTMS (Oncore) implementation / integration

Education & Experience

• Bachelors Degree in Accounting or Finance
• 2+ years of experience working on clinical trials
• Intermediate knowledge of Excel (PIVOT, VLOOKUP)
• CTMS experience required, preferably in OnCore

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.