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Clinical Development Jobs in Madison, WI (NOW HIRING)

Clinical Instructor

Madison, WI · On-site

$90K/yr

Additional opportunities for professional development and expansion of services are available ... Clinical instructor will share clinical diagnostic duties with two clinical faculty and another ...

Showing results 21-40

Clinical Development information

See Madison, WI salary details

$14

$34

$90

How much do clinical development jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical development in Madison, WI is $34.89, according to ZipRecruiter salary data. Most workers in this role earn between $16.73 and $33.17 per hour, depending on experience, location, and employer.

What is the difference between Clinical Development vs Clinical Research Coordinator?

AspectClinical DevelopmentClinical Research Coordinator
Required CredentialsBachelor's degree, often advanced degrees in life sciences or related fields; certifications like CCRP or RACBachelor's degree in health sciences or related field; certifications like CCRP beneficial
Work EnvironmentPharmaceutical or biotech companies, clinical trial teams, R&D departmentsClinical trial sites, hospitals, research centers
Employer & Industry UsageUsed in pharmaceutical, biotech, and medical device industries during drug development phasesUsed in hospitals, research institutions, and clinical trial sites for managing patient studies

While both roles are involved in clinical trials, Clinical Development focuses on designing and managing the overall drug development process, whereas Clinical Research Coordinators handle the day-to-day operations at trial sites, ensuring protocol adherence and patient coordination.

What is clinical development?

Clinical development is the process by which new pharmaceutical drugs, biologics, or medical devices are tested and evaluated in humans to assess their safety and effectiveness. It typically involves a series of phases (Phase I-IV) of clinical trials, starting with small groups of volunteers and expanding to larger patient populations. The goal is to gather the data needed for regulatory approval and to ensure that new treatments provide benefits that outweigh their risks. Clinical development is a critical step in bringing new therapies from the laboratory to patients.

What do you do in clinical development?

A professional in clinical development designs, manages, and oversees clinical trials to evaluate the safety and effectiveness of new medical treatments or drugs. They coordinate with cross-functional teams, ensure compliance with regulatory standards, and analyze data to support product approval processes. Strong project management skills and knowledge of Good Clinical Practice (GCP) are essential in this role.

What does a clinical development specialist do?

A clinical development specialist designs, manages, and oversees clinical trials to evaluate the safety and effectiveness of new medical treatments or devices. They coordinate with research teams, ensure compliance with regulatory requirements, and analyze data to support product approval processes. Strong knowledge of Good Clinical Practice (GCP) and clinical trial management systems is essential for this role.

What are the key skills and qualifications needed to thrive in clinical development?

To thrive in Clinical Development, you need a strong background in life sciences, clinical trial management, and regulatory compliance, often supported by a relevant degree and experience in clinical research. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are typically required. Excellent communication, problem-solving, and leadership skills help professionals coordinate multidisciplinary teams and adapt to evolving study demands. These skills and qualifications ensure the design, execution, and oversight of safe, effective, and compliant clinical trials essential for successful drug development.

What are some common challenges faced in a clinical development role, and how can I prepare for them?

Professionals in Clinical Development often encounter challenges such as managing complex regulatory requirements, coordinating multi-site clinical trials, and ensuring timely patient recruitment. Staying organized, maintaining clear communication with cross-functional teams, and keeping up-to-date with evolving industry guidelines can help you navigate these hurdles. Developing strong project management and problem-solving skills is also essential for success in this dynamic field.

What are popular job titles related to Clinical Development jobs in Madison, WI?

For Clinical Development jobs in Madison, WI, the most frequently searched job titles are:

What job categories do people searching Clinical Development jobs in Madison, WI look for?

The top searched job categories for Clinical Development jobs in Madison, WI are:

Infographic showing various Clinical Development job openings in Madison, WI 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 $72,562 per year, or $34.9 per hour.

Medical Science Liaison, Oncology - North Central

Corcept Therapeutics

Madison, WI

Full-time

Posted 2 days ago

New


Job description

The Oncology MSL role is an exciting opportunity to work at a well-established pharmaceutical company with a first in class oncology product in a platform extending across multiple therapeutic areas. This role is a chance to join a high performing team that is well-respected in the cross-functional Oncology Business Unit. This will cover the North Central Territory and include territories in the following states: Wisconsin, Minnesota, Nebraska, Iowa, North Dakota, South Dakota.

The MSL team focuses on thought leader engagement, insight gathering, and scientific education and will represent Corcept to the highest ethical and professional standards and in accordance with guidelines, directions, and policies. The MSL will ascribe to the mission, vision, and values of the Medical Affairs Team and the overall Oncology Business Unit.

Responsibilities:

  • Model and promote Corcept's key principles: collaborating effectively, embracing possibilities, following the data, and leading by doing, to build a culture of accountability, innovation, and trust
  • Engage in clinically meaningful scientific discussions with thought leaders and other healthcare providers (HCPs) in gynecological oncology and other malignancies to enhance their knowledge of Corcept and the role of glucocorticoid receptor antagonism in oncology
  • Proactively or responsively, when appropriate requests are made, support Corcept products via health care professional communication and education through in-depth scientific presentations and education
  • Respond to medical inquiries from HCPs in a timely and scientifically accurate manner
  • Engage in scientific exchange on Corcept's non-clinical and clinical trial data as well as the clinical development Consistently ask thoughtful questions or challenge internal/external stakeholders
  • Develop and maintain strong working relationships with thought leaders, patient advocacy organizations, and oncology associations (like GOG and ASCO as well as regional organizations) within the oncology community
  • Capture, analyze, and communicate insights and intelligence from the medical and scientific community in a compliant manner to help inform decisions by Corcept. Communications will clearly and effectively frame insights in a usable manner
  • Support company-sponsored clinical trials, investigator-initiated studies (IIS), scientific communications, publications, clinical and scientific education, advisory boards, and congresses
  • Maintain the highest standards of scientific, clinical, and technical expertise in relevant therapeutic area(s)
  • Able to critically review scientific literature and provide evidence-based insights
  • Demonstrate teamwork and collaboration within Medical Affairs (MA) as well as cross-functionally with Clinical Development, Clinical Operations, Market Access, Marketing, Commercial, Data Analytics, etc. Exchange ideas and knowledge compliantly among Oncology functions. Establish regular channels with colleagues across functions for sharing and synthesizing information
  • Attend and participate in medical conferences, ad boards, and other scientific events. Strategically identify KOLs for participation in ad boards
  • Maintain territory plan. Proactively adapt plans for Team MSL based on changes in the internal / external environment
  • Travel required - approximately 50-70% of the time

Preferred Skills, Qualifications and Technical Proficiencies:

  • Demonstrate strong scientific oncology acumen: therapeutic landscapes, NCCN guidelines, clinical trial data, oncology cooperative groups, NCI/NCCN cancer centers, etc.
  • Exemplify the following core competencies: intellectual curiosity, managing change, teamwork and collaboration, communication, achieving results, decision-making, and clinical and scientific expertise
  • Demonstrate business acumen: has working knowledge of the multi-disciplinary functions involved in a company's drug development process, e.g., clinical development, clinical operations, biostatistics, regulatory, commercial, etc.
  • Exhibit project management skills: can prioritize tasks and goals and ensure the timely, on-target, and within-budget accomplishment of projects
  • Identify resources to accomplish priorities and work with the MA team to ensure resources are available
  • Understand change management and demonstrate adaptability in priorities, goals, and territory
  • Demonstrate proven effective interpersonal and communication skills
  • Provide feedback to the Medical Affairs trainer and Medical Affairs Field Directors to ensure an atmosphere of quality improvement and excellence
  • Demonstrate strong experience with PowerPoint, Word, and Excel; must be able to create and edit content with minimal assistance and an eye for accuracy and detail
  • Experience with Veeva CRM (or other CRM) and Veeva Vault, as well as SharePoint and/or BOX is preferred
  • Must maintain a driving record in accordance with Corcept vehicle policy

Preferred Education and Experience:

  • Advanced degree in clinical or medical science (PhD, MD, PharmD, MSN, PA, NP) required
  • 1-3+ years of MSL experience; 2+ years of oncology experience

 #LI-Remote

The pay range that the Company reasonably expects to pay for this position is $160,000 - $220,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.