VP, Drug Development Services (CNS/ Psychiatry) - REMOTE- US, Ireland, UK ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...
VP, Drug Development Services (CNS/ Psychiatry) - REMOTE- US, Ireland, UK ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...
Experienced in all aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones. * Well organized with ability to handle and ...
Experienced in all aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones. * Well organized with ability to handle and ...
Scientist II, CMC Process Development Verona, Wisconsin, United States
Verona, WI ยท On-site
$95 - $110/hr
Characterize drug product formulations to support clinical dosing and regulatory filings * Review and approve batch records for use at CDMOs * Author and execute formulation characterization ...
Scientist II, CMC Process Development Verona, Wisconsin, United States
Verona, WI ยท On-site
$95 - $110/hr
Characterize drug product formulations to support clinical dosing and regulatory filings * Review and approve batch records for use at CDMOs * Author and execute formulation characterization ...
Located at 726 Heartland Trail, the 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance manufacturing, and biopharmaceutical process development. The site ...
Located at 726 Heartland Trail, the 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance manufacturing, and biopharmaceutical process development. The site ...
Located at 726 Heartland Trail, the 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance manufacturing, and biopharmaceutical process development. The site ...
Located at 726 Heartland Trail, the 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance manufacturing, and biopharmaceutical process development. The site ...
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
Senior Manager, CMC Regulatory Affairs Verona, Wisconsin, United States
Verona, WI ยท On-site
$140 - $170/hr
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
Senior Manager, CMC Regulatory Affairs Verona, Wisconsin, United States
Verona, WI ยท On-site
$140 - $170/hr
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
Associate Scientist I, Analytical Development
$57K - $68K/yr
This role supports analytical testing for drug substance and drug product development. The individual will perform routine laboratory testing, assist with analytical method development and ...
Associate Scientist I, Analytical Development
$57K - $68K/yr
This role supports analytical testing for drug substance and drug product development. The individual will perform routine laboratory testing, assist with analytical method development and ...
An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical ...
An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical ...
Associate Scientist I, Analytical Development
Verona, WI ยท On-site
$57K - $68K/yr
This role supports analytical testing for drug substance and drug product development. The individual will perform routine laboratory testing, assist with analytical method development and ...
Associate Scientist I, Analytical Development
Verona, WI ยท On-site
$57K - $68K/yr
This role supports analytical testing for drug substance and drug product development. The individual will perform routine laboratory testing, assist with analytical method development and ...
Associate Scientist III, Analytical Development
Verona, WI ยท On-site
$78K - $90K/yr
An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical ...
Associate Scientist III, Analytical Development
Verona, WI ยท On-site
$78K - $90K/yr
An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical ...
Packaging Operator
Stevens Point, WI ยท On-site
$16.50 - $20/hr
Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all ...
Packaging Operator
Stevens Point, WI ยท On-site
$16.50 - $20/hr
Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all ...
Material Handler, Packaging- 2nd Shift
$16.50 - $20.25/hr
Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all ...
Material Handler, Packaging- 2nd Shift
$16.50 - $20.25/hr
Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all ...
Packaging Operator - 2nd Shift (temporary-to-permanent)
Stevens Point, WI ยท On-site
$16.50 - $20/hr
Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all ...
Packaging Operator - 2nd Shift (temporary-to-permanent)
Stevens Point, WI ยท On-site
$16.50 - $20/hr
Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all ...
Located at 726 Heartland Trail, the 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance manufacturing, and biopharmaceutical process development. The site ...
New
Located at 726 Heartland Trail, the 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance manufacturing, and biopharmaceutical process development. The site ...
New
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
Senior Manager Regulatory Strategy
Pleasant Prairie, WI ยท On-site
$165K - $185K/yr
Liaises with regulatory authorities for all drug development and approval aspects. * Manages the processing of regulatory submissions with Strategy leadership and operational support; ensures ...
Senior Manager Regulatory Strategy
Pleasant Prairie, WI ยท On-site
$165K - $185K/yr
Liaises with regulatory authorities for all drug development and approval aspects. * Manages the processing of regulatory submissions with Strategy leadership and operational support; ensures ...
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
Senior Scientist II, Translational Biomarkers
Madison, WI ยท On-site
$125K - $140K/yr
The Position This Senior Scientist will be part of a team responsible for delivery of translational biomarker strategies for drug development candidates. The ideal candidate will possess in-depth ...
Senior Scientist II, Translational Biomarkers
Madison, WI ยท On-site
$125K - $140K/yr
The Position This Senior Scientist will be part of a team responsible for delivery of translational biomarker strategies for drug development candidates. The ideal candidate will possess in-depth ...
Drug Development information
See Wisconsin salary details
$33.3K - $42.5K
2% of jobs
$42.5K - $51.7K
8% of jobs
$58.7K is the 25th percentile. Wages below this are outliers.
$51.7K - $60.8K
19% of jobs
$60.8K - $70K
20% of jobs
The median wage is $70.3K / yr.
$70K - $79.2K
16% of jobs
$86.3K is the 75th percentile. Wages above this are outliers.
$79.2K - $88.4K
13% of jobs
$88.4K - $97.5K
5% of jobs
$97.5K - $106.7K
11% of jobs
$106.7K - $115.9K
2% of jobs
$115.9K - $125.1K
2% of jobs
$125.1K - $134.2K
2% of jobs
$33.3K
$78.2K
$134.2K
How much do drug development jobs pay per year?
What is drug development?
What are the typical stages of collaboration between different teams in a drug development role?
What are the key skills and qualifications needed to thrive in drug development, and why are they important?
What is the difference between Drug Development vs Pharmacologist?
| Aspect | Drug Development | Pharmacologist |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields; often requires experience in clinical trials | Degree in Pharmacology, Pharmacy, or related fields; may require licensing or certification for clinical practice |
| Work Environment | Research labs, pharmaceutical companies, clinical trial sites | Research labs, hospitals, academic institutions, regulatory agencies |
| Industry Usage | Developing new drugs, overseeing clinical trials, regulatory submissions | Studying 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.
How much do drug development professionals make?
Is drug development a good career?
What career develops drugs?
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For Drug Development jobs in Wisconsin, the most frequently searched job titles are:
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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:

Full-time
Medical, Dental, Vision, Life, Retirement
Posted 8 days ago
Job description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
At ICON, it's our people that set us apart. As a global provider of clinical research services, healthcare intelligence, and consulting solutions, we partner with pharmaceutical, biotechnology, and medical device organizations to accelerate the development of life-changing therapies.
We are seeking an accomplished Vice President, Drug Development Services (CNS/Psychiatry) to serve as a strategic leader and trusted advisor to clients across the pharmaceutical and biotechnology industry. This highly visible role combines therapeutic expertise, scientific leadership, consulting excellence, and business impact to support the successful advancement of CNS and psychiatric therapies from early development through commercialization.
As a senior member of our Drug Development Services (DDS) organization, you will work directly with C-suite executives, Chief Medical Officers, Therapeutic Area Leaders, and senior development teams to design and execute innovative development strategies while leading and inspiring multidisciplinary teams across the global organization.
What You Will Do:
Provide strategic scientific and medical leadership for CNS and Psychiatry development programs spanning Phase I through late-stage clinical development, ensuring robust clinical, regulatory, and commercial strategies.
Serve as a trusted advisor to senior client stakeholders, delivering high-value consulting engagements and guiding critical decisions related to protocol design, development planning, patient selection, endpoints, and overall program strategy.
Lead multidisciplinary Drug Development Services teams, fostering a high-performance culture focused on collaboration, innovation, scientific excellence, and client success.
Drive the design and execution of integrated drug development solutions, including clinical development strategies, feasibility assessments, regulatory planning, risk mitigation, and program optimization.
Build and maintain influential relationships with investigators, key opinion leaders, advisory boards, regulatory agencies, and industry stakeholders to advance client objectives and strengthen ICON's market presence.
Partner closely with Business Development teams to support strategic growth initiatives, including proposal development, client presentations, bid defenses, and scientific leadership during business development activities.
Represent ICON as an industry thought leader through participation in scientific conferences, professional organizations, client forums, and external speaking engagements.
Your Profile
MD with specialization in Neurology, Psychiatry, or a closely related CNS discipline.
10+ years of progressive leadership experience in drug development, with significant expertise in CNS and psychiatric therapeutic areas across pharmaceutical, biotechnology, or CRO environments.
Demonstrated success advancing assets through multiple stages of development, including clinical, regulatory, and strategic decision-making that supports successful development milestones.
Deep understanding of global regulatory requirements and experience guiding development strategies across major regulatory agencies.
Proven ability to influence and build credibility with executive leadership, including CEOs, CMOs, Therapeutic Area Heads, and other senior stakeholders.
Strong experience leading multidisciplinary global teams, including talent development, organizational leadership, budget accountability, and resource management.
Commercially minded strategic consultant with a successful track record supporting business growth, client engagements, and complex drug development partnerships.
Extensive professional network within the pharmaceutical, biotechnology, academic, and regulatory communities
Live in the US, UK, or Ireland with ability to travel up to 25%.
#LI-REMOTE
#LI-LE1
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.
Are you a current ICON Employee? Please click here to apply