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Clinical Trial Associate Jobs in Wisconsin (NOW HIRING)

Associate or Bachelor's degree in Nursing with current state licensure. CPR/AED certification. ACLS ... Support clinical trial operations and participant care. Maintain compliance with safety and quality ...

... trial conducted at the Wisconsin Sleep Center. Responsibilities include IV placement and ... Associate Degree in Nursing (ADN) required. * Bachelor of Science in Nursing (BSN) preferred. How ...

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Clinical Trial Associate information

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$17

$40

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How much do clinical trial associate jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical trial associate in Wisconsin is $40.36, according to ZipRecruiter salary data. Most workers in this role earn between $32.50 and $44.42 per hour, depending on experience, location, and employer.

What Is a Clinical Trial Associate?

A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

What are the key skills and qualifications needed to thrive as a Clinical Trial Associate, and why are they important?

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These competencies are crucial for ensuring compliance, accurate data management, and smooth coordination of clinical trial activities.

What are some common challenges faced by Clinical Trial Associates when managing study documentation?

Clinical Trial Associates often encounter challenges related to maintaining accurate and up-to-date trial documentation, as protocols and regulatory requirements can change frequently. Ensuring all documents are correctly filed, version-controlled, and accessible for audits requires strong attention to detail and organizational skills. Additionally, coordinating with multiple stakeholders—such as clinical research coordinators, data managers, and regulatory teams—can add complexity to document management. Proactive communication and adopting robust documentation systems can help overcome these challenges.

What does a Clinical Trial Associate do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and management of clinical trials. They help ensure studies comply with regulatory requirements and assist in maintaining trial documentation, tracking study progress, and communicating with clinical sites. CTAs work closely with clinical research teams, sponsors, and vendors to keep trials running smoothly and efficiently. Their administrative and logistical support is essential for successful clinical research.

What is the difference between Clinical Trial Associate vs Clinical Research Coordinator?

AspectClinical Trial AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRABachelor's degree in health sciences or related field; similar certifications
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
ResponsibilitiesAssist in trial setup, data collection, regulatory complianceManage patient recruitment, conduct visits, data entry
Industry UsageCommon in pharmaceutical and biotech industriesCommon in hospitals and academic research settings

Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Trial jobs in Wisconsin? The most popular types of Clinical Trial jobs in Wisconsin are:
What are popular job titles related to Clinical Trial Associate jobs in Wisconsin? For Clinical Trial Associate jobs in Wisconsin, the most frequently searched job titles are:
What cities in Wisconsin are hiring for Clinical Trial Associate jobs? Cities in Wisconsin with the most Clinical Trial Associate job openings:
Associate Director for Clinical Trial Operations and Workforce Development

Associate Director for Clinical Trial Operations and Workforce Development

Medical College of Wisconsin

Milwaukee, WI

Full-time

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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