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Codify Therapeutics Jobs in Florida (NOW HIRING)

Codify Therapeutics information

What is the difference between Codify Therapeutics vs Clinical Research Associate?

AspectCodify TherapeuticsClinical Research Associate
Required CredentialsTypically requires a background in life sciences, biology, or pharmacy; degrees such as BS or MS often preferredRequires a degree in life sciences, nursing, or related fields; certifications like CCRA can be advantageous
Work EnvironmentResearch labs, biotech companies, or pharmaceutical firms focused on drug developmentClinical trial sites, hospitals, or research organizations overseeing patient studies
Employer & Industry UsageBiotech and pharmaceutical companies involved in innovative drug researchContract research organizations, pharmaceutical companies, and clinical trial sites

While Codify Therapeutics focuses on drug discovery and development within biotech settings, Clinical Research Associates primarily manage and monitor clinical trials at research sites. Both roles require a background in life sciences but differ in daily responsibilities and work environments.

What are the key skills and qualifications needed to thrive as a therapeutic coder, and why are they important?

To thrive as a Therapeutic Coder, you need a strong understanding of medical terminology, anatomy, and coding systems such as ICD-10 and CPT, usually supported by a relevant certification like CPC or CCS. Familiarity with electronic health records (EHR) systems and coding software is essential for efficient and accurate documentation. Attention to detail, analytical thinking, and effective communication are valuable soft skills that help ensure coding accuracy and collaboration with healthcare teams. These skills are crucial for maintaining compliance, optimizing reimbursement, and supporting patient care quality within healthcare organizations.

What typical collaborations can a professional at Codify Therapeutics expect, and how do these impact daily workflows?

At Codify Therapeutics, professionals often work closely with multidisciplinary teams, including researchers, data scientists, clinicians, and regulatory experts. Collaboration is essential for integrating scientific discoveries with data-driven solutions to accelerate drug development. Daily workflows involve regular cross-functional meetings, project updates, and shared problem-solving, which foster innovation and ensure alignment with project goals. This collaborative environment helps employees build a broad skill set and deepen industry knowledge by working alongside experts from various fields.

What is Codify Therapeutics?

Codify Therapeutics is a biotechnology company focused on developing gene therapy solutions for rare and complex diseases. They use advanced gene editing and delivery technologies to create innovative treatments that address unmet medical needs. The company's research often involves collaborations with academic institutions and pharmaceutical partners to accelerate the development of new therapies. Their mission is to improve patient outcomes by translating cutting-edge science into effective medicines.

What job categories do people searching Codify Therapeutics jobs in Florida look for?

The top searched job categories for Codify Therapeutics jobs in Florida are:

What cities in Florida are hiring for Codify Therapeutics jobs?

Cities in Florida with the most Codify Therapeutics job openings:

Infographic showing various Codify Therapeutics job openings in Florida as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Cell & Gene Therapy Benefits Specialist

Shields Advanced Therapies

Tampa, FL • On-site

$65K - $80K/yr

Full-time

Re-posted 22 days ago


Job description

About Shields Advanced TherapiesShields Advanced Therapies partners with health systems to accelerate advanced therapy access and operations, ensuring life-changing breakthroughs reach more patients. Our management services and technology solutions serve as a horizontal support hub to empower health system- led, world-class advanced therapy care across 50+ disease states. Launched in September 2024, Shields Advanced Therapies is anchored by partnerships with five of the Top 20 Academic Medical Centers in the United States. Additionally, Shields' track record partnering with over 1,000 hospitals across 43 states in prior ventures provides a national channel for expansion.Role OverviewThe Cell & Gene Therapy Benefits Specialist will play a crucial role in managing and coordinating patient financial services, ensuring that patients understand and can access available financial resources from payers, manufacturers, and foundations. The role will report to the Director, Clinical Operations.Core Responsibilities:Benefits Investigation & Verification: Work with all payers (Government, Commercial, and otherwise, including out-of-state Medicaid agencies), pharmacy benefit managers (PBMs) and third-party administrators (TPAs) to identify, investigate and verify patient insurance coverage and benefits as early as possible within the care journey to ensure timely access to care, accurate billing, and minimal claim denials. This involves confirming eligibility and understanding the specifics of various insurance plans, including site-of-care considerations.Prior Authorization Facilitation: Work with patient, Cell & Gene Therapy Clinical Coordinators, clinical staff, payer, and others to secure prior authorizations for each component of the treatment plan as applicable/required.Benefit Enrollment Assistance (if applicable): Guide patients through the process of enrolling in appropriate benefit programs, such as Medicaid, Medicare, or other financial assistance options. This may involve helping patients complete necessary applications and providing information on program requirements.Patient Financial Counseling: Assist patients in understanding their insurance benefits, out-of-pocket costs, and available financial assistance programs. This includes explaining coverage details and guiding patients through the complexities of healthcare billing, including site-of-care considerations.Collaboration with Departments: Work closely with clinical staff, patient accounting, billing & collections, and other hospital departments (e.g., research) to communicate benefits considerations and serve as point of contact during financial clearance process, ensure accuracy, and enhance patient satisfaction. This collaboration ensures that financial considerations are integrated into patient care planning.Collaboration with Manufacturers: In partnership with the Cell & Gene Therapy Clinical Coordinators, work with manufacturers to attempt securing additional financial assistance as applicable/appropriate.Compliance and Documentation: Maintain accurate records of patient interactions, financial agreements, and assistance provided, ensuring compliance with healthcare regulations and privacy laws. This includes documenting all financial counseling sessions and maintaining confidentiality of patient information.Development and Execution of Financial Pathways: Codify and execute benefits investigation and prior authorization pathways tailored to each product covered by advanced therapy programs across Health System Partner's service lines and therapeutic programs.Programmatic Expansion: Contribute to development of centralized Benefits Specialist function that will augment dedicated teams at our Health System Partners and other future partners.Experience:The ideal candidate will have 5+ years of experience in healthcare billing, insurance coordination, or patient financial counseling, and familiarity with healthcare financial systems and the insurance verification process.Strong communication and interpersonal skills are crucial for effectively assisting patients, and attention to detail, organizational abilities, and proficiency with healthcare information systems are also important.Prior experience/familiarity with payer navigation specifically related to cellular therapy (CAR T, TIL, etc.), gene therapy, and/or bone marrow transplant patient journeys and applicable prior authorizations required to enable is preferred.Prior exposure with both inpatient & outpatient site-of-care also preferred but not required. 
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