ZipRecruiter

Log In

1

Drug Development Jobs in Wisconsin (NOW HIRING)

Revvity

Product Applications Specialist

Madison, WI · On-site

... the drug development and therapeutic value chain, particularly in the area of precision medicine. The key focus of the Product Applications Specialist is to deliver on the revenue targets by ...

Uline

Software Development Manager

Pleasant Prairie, WI

$121K - $160K/yr

Software Development Manager Pay from $121,000 to $160,000 per year Corporate Headquarters 12575 ... Uline is a drug-free workplace. All new hires must complete a pre-employment hair follicle drug ...

ULINE

Software Development Manager

Pleasant Prairie, WI · On-site

$121K - $160K/yr

Software Development Manager Pay from $121,000 to $160,000 per year Corporate Headquarters 12575 ... Uline is a drug-free workplace. All new hires must complete a pre-employment hair follicle drug ...

previous page

Showing results 41-60

All JobsDrug Development JobsDrug Development Jobs in Wisconsin

Drug Development information

See Wisconsin salary details

$33.3K

$78.2K

$134.2K

How much do drug development jobs pay per year?

As of Aug 9, 2026, the average yearly pay for drug development in Wisconsin is $78,163.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,000.00 and $91,300.00 per year, depending on experience, location, and employer.

What career develops drugs?

A career in drug development typically involves roles such as pharmacologist, medicinal chemist, clinical researcher, or regulatory affairs specialist. These professionals work in laboratories, research institutions, or pharmaceutical companies to discover, test, and bring new drugs to market, often requiring knowledge of biology, chemistry, and regulatory processes.

What is the difference between Drug Development vs Pharmacologist?

AspectDrug DevelopmentPharmacologist
Required CredentialsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields; often requires experience in clinical trialsDegree in Pharmacology, Pharmacy, or related fields; may require licensing or certification for clinical practice
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial sitesResearch labs, hospitals, academic institutions, regulatory agencies
Industry UsageDeveloping new drugs, overseeing clinical trials, regulatory submissionsStudying drug effects, mechanisms, safety, and efficacy; advising on drug use

While both roles are integral to the pharmaceutical industry, Drug Development focuses on creating and bringing new drugs to market through research, testing, and regulatory processes. Pharmacologists primarily study how drugs interact with biological systems, often working in research or clinical settings to understand drug effects and safety. The two roles often collaborate but differ in their core responsibilities and career focus.

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

To thrive in Drug Development, you need a strong background in pharmaceutical sciences, biology, or chemistry, often supported by an advanced degree (e.g., PhD, PharmD, or MSc). Familiarity with regulatory compliance, clinical trial management systems, and data analysis software such as SAS or R is typically required. Excellent problem-solving, project management, and cross-functional communication skills help professionals excel in this multidisciplinary field. These competencies ensure that new drugs are developed safely, efficiently, and in accordance with regulatory standards.

What is drug development?

Drug development is the process of bringing a new pharmaceutical drug to market. It involves several stages, including drug discovery, preclinical research, clinical trials, and regulatory approval. Each stage is designed to ensure the safety, efficacy, and quality of the drug before it can be made available to patients. The entire process can take several years and requires collaboration between scientists, clinicians, regulatory agencies, and pharmaceutical companies.

How much do drug development professionals make?

Drug development professionals, including roles such as research scientists and clinical trial managers, typically earn between $70,000 and $130,000 annually, depending on experience, education, and location. Entry-level positions may start lower, while senior roles with advanced skills and certifications can exceed this range.

How do you get into drug development?

To enter drug development, individuals typically need a background in life sciences such as biology, chemistry, or pharmacology, often supported by a relevant bachelor's or advanced degree. Gaining experience through internships, research projects, or entry-level roles in pharmaceutical or biotech companies can be valuable, along with developing skills in laboratory techniques, data analysis, and regulatory compliance.

What are the typical stages of collaboration between different teams in a drug development role?

In drug development, professionals regularly collaborate across multidisciplinary teams, including research scientists, clinical trial coordinators, regulatory affairs specialists, and manufacturing experts. Early stages involve close work with research and discovery teams to identify promising compounds, followed by coordination with clinical teams during trial phases, and finally with regulatory and production teams as the drug moves toward approval and commercialization. Effective communication and cross-functional teamwork are essential, as each stage relies on timely data sharing and joint problem-solving to navigate complex challenges.
What job categories do people searching Drug Development jobs in Wisconsin look for? The top searched job categories for Drug Development jobs in Wisconsin are:
What cities in Wisconsin are hiring for Drug Development jobs? Cities in Wisconsin with the most Drug Development job openings:
Drug Development jobs near you
Infographic showing various Drug Development job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $78,163 per year, or $37.6 per hour.

Senior Scientist I, Analytical Development

Arrowhead Pharmaceuticals

Madison, WI

Full-time

Posted 14 hours ago

Posted today

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

This position is within the Analytical Development (AD) group in the CMC Manufacturing organization. The Senior Scientist I, Analytical Development will provide scientific and technical leadership for analytical activities supporting drug substance and drug product development. This role will lead method development and validation activities and support analytical testing for process development, impurity characterization, GLP toxicology studies, and cGMP clinical trial materials.

The Senior Scientist I will work independently and collaboratively across project teams, serve as an analytical lead for assigned programs, and provide technical guidance and mentorship to less experienced scientists. This position reports to Analytical Development management.

Responsibilities

  • Work independently and collaboratively with project teams to deliver accurate, high-quality analytical results in support of new and ongoing development programs.
  • Provide technical leadership, guidance, and mentorship to junior scientists.
  • Serve as Analytical Project Coordinator or Lead for assigned programs, taking ownership of analytical activities, including planning, prioritizing, and coordinating testing to meet project timelines and deliverables.
  • Independently design, develop, optimize, and validate analytical methods supporting all stages of drug substance/API and drug product development.
  • Develop specifications and test methods for raw materials, in-process materials, intermediates, drug substances, and drug products.
  • Lead analytical activities supporting process development, impurity characterization, GLP toxicology studies, and cGMP clinical trial materials.
  • Analyze and interpret complex analytical data, troubleshoot technical challenges, and recommend appropriate follow-up activities.
  • Prepare and review technical documentation, including analytical test methods, development and validation protocols and reports, SOPs, and presentations.
  • Communicate project status, analytical results, risks, and recommendations to project teams and management.
  • Ensure analytical activities are conducted in accordance with applicable SOPs, cGMP requirements, regulatory guidelines, and industry standards.
  • Contribute to continuous improvement of analytical methods, laboratory practices, and departmental processes.
  • Perform other duties as assigned.

Requirements

  • Ph.D. in Chemistry or a related scientific discipline with 2+ years of relevant experience; M.S. with 10+ years of relevant experience; or B.S. with 12+ years of relevant experience.
  • Demonstrated experience in analytical method development, optimization, qualification, and validation supporting pharmaceutical drug substance and drug product development.
  • Experience developing analytical methods and specifications for raw materials, intermediates, drug substances, and drug products.
  • Demonstrated experience with analytical instrumentation and pharmaceutical development processes.
  • Experience independently analyzing complex data, troubleshooting analytical challenges, and recommending appropriate solutions.
  • Experience leading analytical activities or serving as an analytical representative on cross-functional project teams.
  • Proficiency with analytical techniques and instrumentation such as HPLC, GC, FTIR, UV/Vis, LC/MS, Karl Fischer (KF), and related technologies.
  • Strong knowledge of analytical instrumentation principles, test methodologies, and method validation.
  • Strong understanding of CMC regulatory requirements and applicable cGMP, ICH, and FDA/CDER guidelines.
  • Knowledge of the principles of synthetic organic chemistry.
  • Strong scientific judgment, problem-solving, and data interpretation skills.
  • Excellent organizational skills with the ability to manage multiple priorities and project timelines.
  • Strong written and verbal communication skills.
  • Strong attention to detail and commitment to data quality and integrity.
  • Ability to work effectively both independently and within cross-functional teams.

Preferred

  • Experience providing technical guidance, training, or mentorship to junior scientists.
  • Experience serving as an analytical project lead or coordinator for pharmaceutical development programs.
  • Experience supporting analytical activities across multiple stages of drug development.
  • Demonstrated ability to influence scientific direction and effectively communicate technical recommendations across functions.
Wisconsin pay range
$115,000—$135,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

Candidates must have current, valid authorization to work in the country where this role is located.

California Applicant Privacy Policy