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Biosimilar Jobs (NOW HIRING)

Daymark Health

VP of Medical Economics

Boston, MA

Biosimilar opportunity identification: Build utilization analytics to identify biosimilar conversion opportunities across the oncology drug portfolio; quantify per-episode and savings potential and ...

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Biosimilar information

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How much do biosimilar jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for biosimilar in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What are biosimilars?

Biosimilars are biological medicines that are highly similar to already approved reference biologic drugs, with no clinically meaningful differences in terms of safety, purity, or effectiveness. They are developed once the patent for the original biologic has expired, and undergo rigorous regulatory assessment to ensure their quality. Biosimilars are used to treat a range of diseases, such as cancer and autoimmune disorders, often at a lower cost than the original biologics. They help increase patient access to important therapies and encourage competition in the pharmaceutical market.

What is the difference between Biosimilar vs Pharmacist?

AspectBiosimilarPharmacist
Required CredentialsBiotechnology degree, specialized training in biologicsDoctor of Pharmacy (PharmD), licensure
Work EnvironmentPharmaceutical manufacturing, research labsCommunity pharmacies, hospitals, clinics
Industry UsageBiotech, pharmaceutical companiesHealthcare, retail, hospital settings
Common Search/ComparisonBiologics, biosimilar developmentMedication dispensing, patient counseling

While biosimilars are biologic products similar to original biologic drugs, pharmacists are healthcare professionals who dispense medications and advise patients. Both roles are integral to the pharmaceutical industry but differ in focus, credentials, and work environment.

What are some common challenges faced by professionals working in biosimilar development, and how can they be addressed?

Professionals in biosimilar development often encounter challenges such as navigating complex regulatory requirements, ensuring product comparability, and managing cross-functional collaboration between scientific, clinical, and regulatory teams. Staying updated with evolving guidelines from agencies like the FDA and EMA is crucial, as is fostering open communication across departments to streamline data sharing and decision-making. Proactively engaging in continuous professional development and leveraging cross-disciplinary expertise can help address these challenges and contribute to successful biosimilar product development.

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

To thrive as a Biosimilar Scientist, you need a solid background in biochemistry, molecular biology, or related life sciences, often supported by advanced degrees like an MSc or PhD. Familiarity with analytical techniques (e.g., HPLC, mass spectrometry), regulatory guidelines (FDA, EMA), and quality control systems is essential. Strong problem-solving, teamwork, and communication skills help navigate complex development processes and cross-functional collaboration. These competencies ensure successful biosimilar development, regulatory approval, and product safety.
More about Biosimilar jobs
What states have the most Biosimilar jobs? States with the most job openings for Biosimilar jobs include:
What job categories do people searching Biosimilar jobs look for? The top searched job categories for Biosimilar jobs are:
Biosimilar jobs near you
Infographic showing various Biosimilar job openings in the United States as of July 2026, with employment types broken down into 97% Full Time, 1% Part Time, 1% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $54,791 per year, or $26.3 per hour.
Oncology Prior Authorization Specialist

Oncology Prior Authorization Specialist

TRIARQ Health

Royal Oak, MI • On-site

$16.75 - $22.50/hr

Full-time

Posted 2 days ago

Job description

Description:

The Oncology Authorization Specialist acts as the vital bridge between clinical intent and financial execution. This is not a generalist role; it requires a deep understanding of oncology treatment pathways, including chemotherapy infusions. You will serve as a clinical-financial advocate, ensuring that every patient receives life-saving treatment without delay by masterfully navigating the complex landscape of payer medical policies and NCCN guidelines.


Key Responsibilities & Impact


1. Strategic Authorization Management

  • Clinical Alignment: Review of physician orders against NCCN Guidelines and Compendia to ensure medical necessity is clearly demonstrated before submission.
  • Precision Medicine: Manage authorizations for infusions, injections, and biomarker-driven therapies, ensuring the correct ICD-10 and CPT pairings are utilized.
  • Lifecycle Management: Proactively track authorization lifespans to prevent "gap-in-care" scenarios, managing dosage escalations and regimen changes in real-time.

2. Financial Advocacy & Payor Navigation

  • Payer Expertise: Act as the subject matter expert on Medicare Part B vs. Part D coverage, "Buy and Bill" workflows, and site-of-service differentials.
  • Denial Prevention: Analyze payer medical policies to identify potential hurdles (e.g., step therapy with biosimilars) before they result in denial.
  • Appeals Leadership: Lead the "Letter of Medical Necessity" (LMN) process, partnering with physicians to provide evidence-based arguments for peer-to-peer reviews.

3. Patient-Centric Coordination

  • Time-to-Treat Optimization: Minimize the "days to first treatment" by navigating urgent authorization requests with a sense of clinical urgency.
  • Interdisciplinary Collaboration: Serve as a core member of the care team, providing updates to Nursing and Financial Counselors regarding clearance status.


Requirements:


3+ years of dedicated Oncology authorization or billing experience.

Proficiency in NCCN Guidelines, cancer staging, and the distinction between curative and palliative intent.

Advanced knowledge of HCPCS (J-Codes/Q-Codes), CPT administration codes, and Oncology-specific ICD-10 coding.

Expertise in EMR systems, insurance portals, and clearinghouses.


Preferred Skills for High-Level Candidates

  • Biosimilar Strategy: Understanding the financial and clinical shift toward biosimilar utilization and payer-preferred product lists.
  • Specialty Pharmacy Nuance: Experience managing the "White Bagging" vs. "Brown Bagging" workflows and their impact on clinic revenue and patient safety.
  • Resilience: The ability to remain empathetic yet persistent when navigating the bureaucracy of insurance denials.