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Entry Level Regulatory Affairs Associate Jobs in Wisconsin

SolCur

WI · On-site

$70 - $90/hr

The Medical Affairs Associate supports the execution of medical affairs activities within ... Ensure all scientific communication activities are compliant with local regulations and internal ...

SolCur

WI · On-site

$60 - $75/hr

This role works closely with Clinical Operations, Study Management, Regulatory Affairs, Quality ... The TMF Associate plays a key role in maintaining inspection readiness and supporting the overall ...

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Compliance Analyst I

Milwaukee, WI · On-site +1

Compliance Analyst I Under general supervision, performs one or more entry-level compliance duties on a professional level working with the VP of Compliance, Contracts, and Regulatory Affairs to meet ...

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Compliance Analyst I

Milwaukee, WI · On-site

... entry-level compliance duties on a professional level working with the VP of Compliance, Contracts, and Regulatory Affairs to meet company goals and objectives related to corporate compliance. This ...

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Entry Level Regulatory Affairs Associate information

See Wisconsin salary details

$19

$39

$63

How much do entry level regulatory affairs associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for entry level regulatory affairs associate in Wisconsin is $39.94, according to ZipRecruiter salary data. Most workers in this role earn between $32.02 and $47.31 per hour, depending on experience, location, and employer.

What does an entry level regulatory affairs associate do?

An Entry Level Regulatory Affairs Associate supports the regulatory affairs team by helping to ensure that products comply with all relevant regulations and standards. This often includes preparing and submitting documentation to regulatory agencies, assisting with product registrations, and maintaining records. They also help to monitor changes in regulations and communicate important updates to internal teams. This role is essential for companies in industries like pharmaceuticals, medical devices, and biotechnology to bring products to market legally and efficiently.

What are the key skills and qualifications needed to thrive as an entry level regulatory affairs associate?

To thrive as an Entry Level Regulatory Affairs Associate, you need a background in life sciences or related fields, strong attention to detail, and knowledge of regulatory guidelines and documentation. Familiarity with regulatory submission systems, document management tools, and sometimes certifications like RAC (Regulatory Affairs Certification) can be beneficial. Strong organizational skills, clear written and verbal communication, and the ability to work collaboratively make candidates stand out. These skills and qualifications are essential for ensuring compliance, timely submissions, and effective coordination in the highly regulated healthcare or pharmaceutical industries.

What are some common challenges faced by entry level regulatory affairs associates when adapting to regulatory changes?

Entry Level Regulatory Affairs Associates often encounter the challenge of staying up to date with frequent changes in local and international regulations. Adapting quickly requires strong research skills and attention to detail, as new guidelines can impact submission processes or product compliance. Collaborating closely with cross-functional teams, such as quality assurance and product development, is essential to ensure that all documentation aligns with the latest requirements. Proactively seeking mentorship and participating in training sessions can help new associates navigate these shifts more efficiently.

What is the difference between Entry Level Regulatory Affairs Associate vs Regulatory Affairs Specialist?

AspectEntry Level Regulatory Affairs AssociateRegulatory Affairs Specialist
QualificationsBachelor's degree in life sciences or related field; some certifications optionalBachelor's or master's degree; certifications like RAC beneficial
Work EnvironmentEntry-level, supporting regulatory documentation and researchMore independent, managing submissions and compliance strategies
Industry UsageCommonly used for early-career roles in pharma, biotech, medical devicesUsed for mid-level roles with increased responsibilities

Entry Level Regulatory Affairs Associates typically handle foundational tasks like document preparation and research, requiring basic industry knowledge. Regulatory Affairs Specialists have more experience, managing submissions and compliance strategies. Both roles are essential in regulated industries like pharmaceuticals and medical devices, but the Specialist role involves greater responsibility and independence.

What are popular job titles related to Entry Level Regulatory Affairs Associate jobs in Wisconsin?

For Entry Level Regulatory Affairs Associate jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Entry Level Regulatory Affairs Associate jobs in Wisconsin look for?

The top searched job categories for Entry Level Regulatory Affairs Associate jobs in Wisconsin are:

What cities in Wisconsin are hiring for Entry Level Regulatory Affairs Associate jobs?

Cities in Wisconsin with the most Entry Level Regulatory Affairs Associate job openings:

Entry Level Regulatory Affairs Associate jobs near you
Infographic showing various Entry Level Regulatory Affairs Associate job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 26% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,077 per year, or $39.9 per hour.

Medical Affairs Associate

SolCur

WI • On-site

$70 - $90/hr

Other

Posted 4 days ago

Job description

The Medical Affairs Associate supports the execution of medical affairs activities within cardiometabolic and metabolic disease areas, including diabetes and obesity. The role combines scientific expertise with cross-functional collaboration and contributes to the development and implementation of medical strategies aligned with product and disease area objectives. Responsibilities may include scientific communication, stakeholder engagement, project coordination, medical education initiatives, review of promotional materials, and support of field-based teams. The position also involves contributing to advisory boards, congress activities, medical training, and scientific exchange with healthcare professionals, while ensuring compliance with applicable regulations and internal standards.

Main activities are: Medical & Cross-Functional Support
  • Build and maintain strong knowledge of products, disease areas, and treatment landscapes within the assigned therapeutic area.
  • Support the development and execution of local medical strategies aligned with broader product and disease area objectives.
  • Collaborate closely with cross-functional stakeholders including Medical Affairs, Commercial, Market Access, Clinical Operations, Real-World Evidence, and Regulatory teams.
  • Contribute scientific input to promotional and educational materials in line with applicable regulations and internal processes.
  • Support internal medical and scientific training initiatives for commercial and field-based teams.
  • Monitor developments within the healthcare landscape and assess their potential impact on medical activities and patient care.
Scientific Exchange & Medical Communication
  • Ensure all scientific communication activities are compliant with local regulations and internal standards.
  • Respond to scientific inquiries from healthcare professionals when appropriate.
  • Support scientific exchange through educational meetings, scientific presentations, and congress-related activities.
  • Assist in the organization of advisory boards and expert meetings.
  • Prepare and maintain scientific slide decks, presentations, and supporting materials.
Scientific Expertise & Continuous Learning
  • Stay up to date with clinical developments, treatment guidelines, and scientific literature within the therapeutic area.
  • Critically evaluate emerging data and maintain awareness of competitor developments and evolving medical trends.
  • Identify potential evidence gaps and contribute to initiatives supporting scientific understanding and patient access.
General Responsibilities
  • Support project coordination and follow-up of timelines and budgets.
  • Participate in local and international internal initiatives.
  • Contribute to a patient-centric and science-driven culture.
Qualifications
  • Master’s degree in a scientific or life sciences field.
  • Previous experience in Medical Affairs is considered an advantage.
  • Experience or interest in endocrinology, metabolism, or cardiometabolic diseases is a plus.
  • Fluent in English and either Dutch or French; knowledge of all three languages is an asset.
  • Strong scientific literacy and ability to interpret medical literature.
  • Excellent communication and interpersonal skills.
  • Comfortable collaborating across multiple departments and stakeholders.
  • Strong organizational and project management capabilities.
  • Able to manage multiple priorities in a dynamic environment.
  • Good command of standard digital and office tools.
What we offer:
  • We offer a competitive salary package with extra-legal benefits: possibility to telework and have flexible working hours, 32 days of holiday per year, full electric company car and charging card, hospitalization and group insurance, lunch vouchers, eco vouchers, mobile phone (data included).
  • We commit to support you to perform your assignment under the best conditions (personal coaching, job-relevant support / training, 360 degree year end review, ...).
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