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Associate Director Clinical Research Jobs in Wisconsin

Clinical Research Nurse Perform clinical assessments including blood pressure, venipuncture, weight ... Associate or Bachelor's degree in Nursing with current state licensure. CPR/AED certification. ACLS ...

Clinical Research Analyst

Madison, WI · On-site

$43.27 - $48.08/hr

Job Summary Our client seeks a Clinical Research Analyst responsible for conducting and managing ... direct patient care, accessing medical and confidential records, access to prescription medication ...

Clinical Research Coordinator

Racine, WI

$22.75 - $30.25/hr

... and clinical aspects of multiple research projects. * Collaborate with primary investigator ... We empower our 99,000+ associates to bring their skills and expertise every day to reimagining ...

We empower our 99,000+ associates to bring their skills and expertise every day to reimagining ... and clinical aspects of multiple research projects. * Collaborate with primary investigator ...

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Showing results 1-20

Associate Director Clinical Research information

See Wisconsin salary details

$25.6K

$140.8K

$271.7K

How much do associate director clinical research jobs pay per year?

As of May 28, 2026, the average yearly pay for associate director clinical research in Wisconsin is $140,750.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,117.00 and $178,517.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Associate Director Clinical Research, and why are they important?

To thrive as an Associate Director Clinical Research, you need advanced knowledge of clinical trial design, regulatory compliance, and drug development, typically supported by a relevant advanced degree and significant industry experience. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and familiarity with GCP and FDA/EMA regulations are crucial. Strong leadership, strategic thinking, and excellent communication skills help build effective teams and manage complex projects. These skills ensure successful, compliant clinical trials that advance organizational goals and safeguard patient safety.

What are some typical challenges faced by an Associate Director of Clinical Research when leading cross-functional teams?

As an Associate Director of Clinical Research, you may encounter challenges such as aligning priorities across diverse functional groups (e.g., regulatory, data management, and clinical operations), managing tight timelines, and ensuring clear communication among stakeholders. Navigating regulatory requirements and adapting to evolving study protocols also require strong problem-solving skills. Success in this role often depends on your ability to foster collaboration and maintain focus on project goals while balancing the needs of multiple departments.

What does an Associate Director of Clinical Research do?

An Associate Director of Clinical Research is responsible for overseeing the planning, execution, and management of clinical trials within a pharmaceutical or biotechnology company. They ensure that all research activities comply with regulatory requirements, company policies, and ethical standards. Their role often includes supervising clinical project teams, managing budgets and timelines, and liaising with external partners such as contract research organizations (CROs) and regulatory agencies. Additionally, they play a key part in developing clinical study protocols, monitoring trial progress, and ensuring data integrity for successful drug development.

What is the difference between Associate Director Clinical Research vs Clinical Project Manager?

AspectAssociate Director Clinical ResearchClinical Project Manager
CredentialsTypically requires a PhD, MD, or advanced degree in life sciences; relevant certifications like RAC or CCRP are commonBachelor's or master's degree in life sciences or related field; certifications like PMP are advantageous
Work EnvironmentLeads multiple clinical trials, oversees teams, and collaborates with senior management in pharmaceutical or biotech companiesManages specific clinical trials, coordinates teams, and ensures project milestones are met within clinical research settings
Employer & Industry UsageUsed in pharmaceutical, biotech, and CROs for senior clinical research leadership rolesCommonly employed in pharmaceutical companies and CROs for trial management

The Associate Director Clinical Research typically holds a higher strategic and leadership role, overseeing multiple projects and teams, whereas the Clinical Project Manager focuses on the day-to-day management of individual clinical trials. Both roles require strong knowledge of clinical research processes, but the Associate Director often has more seniority and broader responsibilities.

What are popular job titles related to Associate Director Clinical Research jobs in Wisconsin? For Associate Director Clinical Research jobs in Wisconsin, the most frequently searched job titles are:
Infographic showing various Associate Director Clinical Research job openings in Wisconsin as of May 2026, with employment types broken down into 100% Full Time. Highlights an 70% In-person, and 30% Remote job distribution, with an average salary of $140,750 per year, or $67.7 per hour.
Associate Director for Clinical Trial Operations and Workforce Development

Associate Director for Clinical Trial Operations and Workforce Development

Medical College of Wisconsin

Milwaukee, WI

Other

Medical, Dental, Vision, Retirement, PTO

Posted 27 days ago


Medical College Of Wisconsin rating

8.2

Company rating: 8.2 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

106th of 528 rated colleges and universities


Job description

Summary

The Associate Director for Clinical Trial Operations and Workforce Development provides strategic and operational leadership for clinical trial activities within the Clinical and Translational Science Institute (CTSI) at the Medical College of Wisconsin (MCW). This position oversees the CTSI Clinical Trials Office and the Adult Translational Research Unit (A-TRU), ensuring excellence in clinical research operations, compliance, and staff development.
The incumbent will build and lead systems that promote transparency, accountability, and efficiency in clinical research conduct. They will collaborate with institutional and national partners to advance MCW's clinical research enterprise by reducing trial activation times, enhancing operational quality, and ensuring alignment with NIH and MCW policies. This individual will serve as an architect and catalyst for institutional improvement in clinical trial processes-developing dashboards, standard operating procedures (SOPs), educational resources, and performance metrics to strengthen the overall clinical trial portfolio at MCW.

Primary Responsibilities

  • Provide strategic direction and operational leadership for the CTSI Clinical Trials Office and Adult Translational Research Unit.
  • Supervise clinical trial operations staff, ensuring alignment with MCW's mission, policies, and NIH guidelines.
  • Foster a culture of continuous improvement, collaboration, and accountability in clinical trial operations.
  • Ensure high-quality, compliant, and efficient conduct of clinical trials across MCW research sites.
  • Oversee adherence to institutional, NIH, FDA, and other regulatory requirements related to human subjects research.
  • Develop and implement SOPs, quality metrics, and monitoring processes to promote compliance and operational integrity.
  • Lead the design and implementation of CTSI training and credentialing programs for clinical research staff across the consortium.
  • Coordinate hiring and milestone achievement for promotion for clinical research staff.
  • Develop and disseminate educational materials and resources to support staff competency and professional growth.
  • Establish systems for continuous learning, best practice sharing, and workforce development across clinical research teams.
  • Design and maintain systems to measure, report, and optimize clinical trial performance.
  • Develop dashboards and analytical tools to track trial activation, enrollment, and compliance metrics.
  • Implement transparent reporting mechanisms to inform leadership decision-making and resource allocation.
  • Provide financial oversight for the CTSI Clinical Trials Office and A-TRU.
  • Ensure efficient resource utilization, budget management, and cost recovery across operational areas.
  • Collaborate with institutional finance partners to support sustainable growth and operational efficiency.
  • Partner closely with the CTSI Managing Director, and Director, and Senior Associate Directors to align operational strategies with the broader CTSI mission and CTSA grant objectives.
  • Engage with key institutional stakeholders-including investigators, department leaders, and compliance offices-to strengthen clinical trial infrastructure.
  • Represent MCW and the CTSI in local and national discussions on clinical trial management and translational research best practices.

Knowledge - Skills - Abilities

  • Demonstrated success in building systems that improve trial activation timelines, operational efficiency, and data transparency.
  • Deep understanding of NIH, FDA, and GCP compliance standards.
  • Proven ability to lead cross-functional teams and foster a collaborative research culture.
  • Experience with financial oversight and performance-based management of research operations.
  • Strong analytical, strategic planning, and communication skills.
  • Understanding of financial and human resources related issues.
  • Excellent project management skills.
  • Excellent oral and written communication skills (interpersonal, customer focus).
  • Strong critical thinking, problem solving and attentiveness to detail required.
  • Ability to build/foster strong, trusting relationships.

Qualifications

Appropriate experience may be substituted on equivalent basis.

Minimum Required Education: Bachelor's Degree

Minimum Required Experience: Minimum of 7 years of progressive experience in clinical research operations, with leadership responsibility in a complex academic or health system environment.

Preferred Education: Master's degree in a related field preferred (e.g., Health Administration, Clinical Research, or equivalent)

Preferred Experience: Academic Medical/Research Environment

Physical Requirements

Work requires occasionally lifting moderate weight materials, standing, or walking continuously.

Work Environment

Little or no exposure to hazards such as dust, fumes, or extreme temperatures, airborne or blood borne pathogens, extreme temperatures, or allergens.

Sensory Acuity

Ability to detect and translate speech or other communication required. May occasionally require the ability to distinguish colors and perceive relative distances between objects.

Why MCW?
  • Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental. Along with Flexible Spending options

  • 403B Retirement Package

  • Competitive Vacation and Paid Holidays offered

  • Tuition Reimbursement

  • Paid Parental Leave

  • Employee & Family Assistance Program (EFAP)

  • Pet Insurance

  • On campus Fitness Facility, offering onsite classes

  • Additional discounted rates on items such as: Select cell phone plans, local fitness facilities, Milwaukee recreation and entertainment etc.

For a brief overview of our benefits see: Benefits Overview

For a full list of positions see: MCW Careers
At MCW all of our endeavors, from our internal operations to our interactions with our partners, are driven by our shared organizational values: Caring - Collaborative - Curiosity - Inclusive - Integrity - Respect. We are committed to fostering an inclusive environment that values diversity in backgrounds, experiences, and perspectives through merit-based processes and in alignment with all applicable laws. We believe that embracing human differences is critical to realize our vision of a healthier world, and we recognize that a healthy and thriving community starts from within. Our values define who we are, what we stand for and how we conduct ourselves at MCW. If you believe in embracing individuality and working together according to these principles to improve health for all, then MCW is the place for you. For more information, please visit our institutional website.


MCW as an Equal Opportunity Employer and Commitment to Non-Discrimination:

The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer. We are committed to fostering an inclusive community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race, color, national origin, religion, age, disability, sex, gender identity/expression, sexual orientation, marital status, pregnancy, predisposing genetic characteristic, or military status. Employees, students, applicants or other members of the MCW community (including but not limited to vendors, visitors, and guests) may not be subjected to harassment that is prohibited by law or treated adversely or retaliated against based upon a protected characteristic.


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About Medical College of Wisconsin

Sourced by ZipRecruiter

The Medical College of Wisconsin (MCW) is an industry-leading educational institution located in Milwaukee, WI, US. Being part of the medical and health services sector, MCW's primary mission is to educate and train the next generation of healthcare professionals. MCW offers a wide array of degrees and programs within medical and health sciences, covering everything from medical, graduate, pharmacy and health sciences studies, to continuing professional developments and community engagement initiatives. Founded in 1893, MCW boasts a rich, well-entrenched history in shaping the medical education landscape locally and globally. The institution's core values of knowledge-changing life underline its dedication to incorporating innovative approaches in education and research, commitment to diversity and inclusion, service to the community, integrity, stewardship, and collaboration.

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Milwaukee, WI, US

Year founded

1893

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