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Biosimilars Jobs (NOW HIRING)

Guidehouse

Bioassay Researcher

Silver Spring, MD

$85K - $141K/yr

Establish new analytical methods to evaluate the biological activity of biotechnology products, biosimilars, and complex generics. * Collect, process, analyze, and document laboratory data from ...

New

Biosimilar Sciences PR LLC

PR · On-site

Provide strategic leadership for Analytical Sciences across development, tech transfer, validation, and commercial testing activities for biologics, biosimilars, and peptides. * Lead and oversee ...

Guidehouse

Bioassay Researcher

Silver Spring, MD · On-site

$85K - $141K/yr

Establish new analytical methods to evaluate the biological activity of biotechnology products, biosimilars, and complex generics. * Collect, process, analyze, and document laboratory data from ...

New

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Biosimilars information

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$150K

$188.7K

$232.5K

How much do biosimilars jobs pay per year?

As of Jul 17, 2026, the average yearly pay for biosimilars in the United States is $188,749.00, according to ZipRecruiter salary data. Most workers in this role earn between $167,500.00 and $210,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Biosimilars position, and why are they important?

To thrive in a Biosimilars role, you typically need a background in life sciences or pharmacy, in-depth understanding of biologic drug development, and knowledge of regulatory requirements such as those from the FDA or EMA. Familiarity with laboratory techniques, clinical trial management systems, and compliance software is highly valuable, along with certifications in clinical research or regulatory affairs. Excellent analytical skills, attention to detail, and the ability to work collaboratively across multidisciplinary teams set top candidates apart. These skills are crucial to ensure strict adherence to regulatory standards and to bring safe, effective biosimilar therapies to market efficiently.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior executive roles such as Chief Medical Officer, Vice President of Research and Development, or Chief Scientific Officer tend to be the highest paying jobs. These positions require extensive experience, advanced degrees, and leadership skills, often offering compensation packages that include high salaries, bonuses, and stock options.

What are some common challenges faced by professionals working in biosimilars development and how are they addressed?

Professionals in biosimilars development often face challenges such as navigating complex regulatory pathways, demonstrating biosimilarity to reference biologics, and ensuring consistent product quality throughout manufacturing. Teams address these challenges by maintaining close communication with regulatory agencies, applying rigorous analytical methods, and implementing strong quality assurance processes. Collaboration across regulatory, clinical, and manufacturing departments is essential to successfully bring a biosimilar to market. Staying updated on evolving industry standards and regulatory expectations is also key to overcoming obstacles in this fast-paced field.

What biology jobs pay over $100k?

In the field of biosimilars, roles such as senior regulatory affairs managers, clinical development directors, and biopharmaceutical project leaders often have salaries exceeding $100,000. These positions typically require advanced degrees, extensive industry experience, and skills in regulatory compliance, project management, or scientific research.

What is a Biosimilars job?

A Biosimilars job typically involves working in the development, manufacturing, regulation, or commercialization of biosimilar medicines—biological products that are highly similar to approved reference biologics. Professionals in this field may work in areas such as research and development, quality control, clinical trials, regulatory affairs, or marketing. Roles can include scientists, regulatory specialists, project managers, or sales professionals, depending on the company and stage of product development. The goal of a biosimilars job is to ensure these medicines meet rigorous safety, efficacy, and quality standards while providing more affordable treatment options for patients.

Do biosimilars work as well?

Biosimilars are highly similar to original biologic drugs and have been shown through clinical trials to be as effective and safe as their reference products. Regulatory agencies like the FDA and EMA approve biosimilars based on rigorous testing, ensuring they provide comparable therapeutic outcomes. As a biosimilars specialist, understanding these standards is essential for evaluating their efficacy in treatment plans.

What jobs pay 500,000 a year in the US?

In the field of biosimilars, executive roles such as Chief Medical Officers, Vice Presidents, or senior pharmaceutical executives can reach or exceed $500,000 annually, especially with bonuses and stock options. These positions typically require extensive industry experience, advanced degrees, and leadership skills in biotech or pharmaceutical companies.
More about Biosimilars jobs
What are the most commonly searched types of Biosimilars jobs? The most popular types of Biosimilars jobs are:
What states have the most Biosimilars jobs? States with the most job openings for Biosimilars jobs include:
What job categories do people searching Biosimilars jobs look for? The top searched job categories for Biosimilars jobs are:
Biosimilars jobs near you
Infographic showing various Biosimilars job openings in the United States as of July 2026, with employment types broken down into 87% Full Time, and 13% Part Time. Highlights an 100% In-person job distribution, with an average salary of $188,749 per year, or $90.7 per hour.

Clinical Development Scientist - Biosimilars

AdvanzPharma

OR • On-site, Remote

Other

Re-posted 15 days ago

Job description

Job Title:

Lead Clinical Development Scientist - Biosimilars

Location:

  • UK - Remote 
  • Spain - Remote 

About the Role

As ADVANZ PHARMA sharpens its strategic focus towards biosimilars and specialty generics, we have an exciting opportunity for a Clinical Development Scientist to join our Clinical Development team.

This role will focus primarily on supporting biosimilars development programmes, working closely with internal teams and external partners to ensure partners clinical strategies and programmes are aligned with regulatory expectations and delivered at pace.

This is a hands-on role within a small, high-impact team, offering exposure across clinical development strategy, trial execution, partner governance and regulatory deliverables during an exciting period of growth in the biosimilars space.

What You'll Do:

  • Lead clinical development oversight of partner-led biosimilar programmes, including PK comparability, immunogenicity, safety, and efficacy where applicable.
  • Contribute to clinical development strategy, including study design and programme planning
  • Critically review biosimilar clinical development plans and study designs, ensuring they are aligned with current EMA, FDA, UK, and other relevant regulatory expectations. Review, challenge and refine clinical trial documentation and outputs across biosimilar studies (e.g. PK/PD, immunogenicity)
  • Support preparation and review of clinical and regulatory documents, including briefing materials, submission modules, and health authority responses. Collaborate with cross-functional teams including Regulatory Affairs, Medical Affairs,  Clinical Operations and Business Development to support portfolio decisions.
  • Provide scientific input and support to ensure programmes are delivered efficiently and to high quality
  • Contribute to a fast-paced, evolving clinical development environment

About You

We are looking for a Clinical Scientist with direct biosimilar experience who is ready to take ownership of scientific review and partner oversight within a growing, focused development function. .

You will be comfortable working in a fast-moving environment and contributing across both clinical strategy and execution.

Qualifications:

  • Advanced degree (MSc, PhD, PharmD, MD or equivalent) in a scientific discipline

Knowledge, Skills & Experience:

  • Working experience in clinical development, clinical science, medical science, or a related role within pharma, biotech, or CRO, including direct work on biosimilar development programmes (essential).
  • Hands-on biosimilar development experience, including clinical PK comparability, immunogenicity strategy, study conduct, data interpretation, or filing support (essential).
  • Ability to critically assess bioanalytical and immunogenicity outputs, including PK assay suitability, ADA/NAb data interpretation, sensitivity, specificity, and clinical relevance (desirable)
  • Experience reviewing or contributing to biosimilar clinical development plans, protocols, SAP input, CSRs, briefing books, regulatory responses, or submission documents.
  • Practical knowledge of EMA and/or FDA biosimilar expectations, with the ability to stay current with evolving guidance.
  • Strong understanding of clinical trial methodology from design to reporting
  • Experience contributing to clinical and regulatory documentation
  • Good understanding of GCP and inspection readiness
  • Ability to work effectively in a cross-functional, matrix environment

Why ADVANZ PHARMA?

At ADVANZ PHARMA, we believe that our employees are our greatest asset.

That's why we are committed to creating an environment where every individual can thrive, contribute, and grow. Here's what makes ADVANZ PHARMA an exceptional place to build your career:

A Culture of Empowerment and Belonging
We foster a workplace rooted in continuous learning, inclusivity, and collaboration. Every voice matters, and we strive to ensure our employees feel valued, respected, and empowered to make a difference.

Flexibility and Support for Your Wellbeing
Our agile and flexible working arrangements, paired with a comprehensive compensation and benefits package, are designed to support your health, career aspirations, and worklife balance.

Recognition That Inspires
Through our Rewards and Recognition programme, we celebrate the extraordinary contributions of our team members. From outstanding achievements to daytoday excellence, appreciation is a cornerstone of our culture.

Global Benefits
We offer a comprehensive global benefits package designed to support health, wellbeing, and professional growth, including:

  • Global recognition programme
  • Employee Assistance Programme
  • Birthday leave
  • Annual Wellbeing Day leave
  • Two days' volunteer leave
  • Four weeks working from anywhere
  • Compassionate leave
  • Long Service Award

But don't just take our word for it: 89% of employees in our Q1 2025 engagement survey would recommend ADVANZ PHARMA as a great place to work.

Apply