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Clinical Trial Transparency Associate Jobs in Wisconsin

WI · On-site

$60 - $75/hr

The TMF Associate is responsible for supporting the maintenance, quality, and completeness of the ... Maintain and support the electronic and/or paper Trial Master File (TMF) for one or more clinical ...

WI · On-site

$79.09 - $93/hr

Senior Research Administration Associate - Clinical Trial Billing and Finance * Division ... transparency. By managing complex contracts and financial operations with precision, the role ...

WI · On-site

$80 - $110/hr

Interfaces, collaborates and oversees Clinical Research Associates (CRAs); Oversees and supports the development and execution of Investigator agreements and trial payments; Is responsible for ...

Be Seen First

The ideal candidate will be responsible for running various clinical trial social & digital media ... High school diploma is required, an Associate's or Bachelor's Degree in Marketing, Advertising, or ...

Our associates are involved in every stage of diagnostics, from ideation to development and ... This role is responsible for clinical trial strategies within the US and EU regions for Danaher ...

WI · On-site

$200 - $230/hr

You will interface clinical trial sites, collaborate, and engage opinion leaders to communicate ... EEO Statement We encourage and support equal employment opportunities for all associates and ...

Clinical Research Nurse

Madison, WI · On-site

$51 - $56/hr

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

Strong understanding of clinical trial operations, monitoring practices, investigational product ... associates through our comprehensive Total Rewards program. We are committed to attracting and ...

Strong understanding of clinical trial operations, monitoring practices, investigational product ... associates through our comprehensive Total Rewards program. We are committed to attracting and ...

Strong understanding of clinical trial operations, monitoring practices, investigational product ... associates through our comprehensive Total Rewards program. We are committed to attracting and ...

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Showing results 1-20

Clinical Trial Transparency Associate information

See Wisconsin salary details

$17

$40

$70

How much do clinical trial transparency associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical trial transparency 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 transparency associate?

Clinical Trial Transparency Associates are professionals responsible for ensuring that information about clinical trials is accurately disclosed and publicly available in compliance with regulatory requirements. Their work includes preparing and submitting trial data to clinical trial registries, redacting sensitive information, and supporting the publication of trial results. They help organizations maintain transparency with stakeholders, including patients, regulators, and the scientific community. This role is essential to promote trust, ethical standards, and data sharing in medical research.

What are the key skills and qualifications needed to thrive as a clinical trial transparency associate?

To thrive as a Clinical Trial Transparency Associate, you need a solid understanding of clinical research processes, regulatory requirements (such as FDA, EMA, and ICMJE), and a relevant life sciences degree. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), disclosure platforms, and data anonymization tools is typically required. Exceptional attention to detail, organizational skills, and the ability to communicate complex information clearly are vital soft skills. These competencies ensure accurate and compliant disclosure of clinical trial data, supporting regulatory obligations and public trust in research.

What are some typical challenges faced by a clinical trial transparency associate when managing trial disclosure requirements?

Clinical Trial Transparency Associates often encounter challenges in navigating diverse regulatory requirements across different countries, as disclosure rules can vary significantly by region and sponsor. Coordinating with multiple stakeholders—from clinical teams to legal and regulatory departments—can also be complex, especially when ensuring timely and accurate data submissions. Staying updated on evolving transparency guidelines and managing large volumes of documentation are key aspects of the role. Proactive communication, strong organizational skills, and attention to detail are essential to successfully overcoming these challenges.

What is the difference between Clinical Trial Transparency Associate vs Clinical Data Coordinator?

AspectClinical Trial Transparency AssociateClinical Data Coordinator
Required CredentialsBachelor's degree, knowledge of clinical trial regulationsBachelor's degree, understanding of clinical data management
Work EnvironmentPharmaceutical or biotech companies, CROsResearch sites, hospitals, clinical research organizations
Employer & Industry UsageUsed in clinical trial disclosure and transparency effortsUsed in managing and coordinating clinical data collection
Common Search & Comparison IntentUnderstanding roles in clinical trial transparencyDistinguishing data management roles in clinical research

The Clinical Trial Transparency Associate focuses on ensuring clinical trial data is publicly disclosed in compliance with regulations, while the Clinical Data Coordinator manages and organizes clinical data collection and entry. Both roles require a background in clinical research but serve different functions within the clinical trial process.

What are the most commonly searched types of Clinical Trial Transparency jobs in Wisconsin?

The most popular types of Clinical Trial Transparency jobs in Wisconsin are:

What are popular job titles related to Clinical Trial Transparency Associate jobs in Wisconsin?

For Clinical Trial Transparency Associate jobs in Wisconsin, the most frequently searched job titles are:

What cities in Wisconsin are hiring for Clinical Trial Transparency Associate jobs?

Cities in Wisconsin with the most Clinical Trial Transparency Associate job openings:

Director, Clinical Trial Activation & Quality Office - Research Office

Medical College of Wisconsin

Milwaukee, WI • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago


Medical College Of Wisconsin rating

7.7

Company rating: 7.7 out of 10

Based on 29 frontline employees who took The Breakroom Quiz

265th of 629 rated colleges and universities


Job description

Summary

The Medical College of Wisconsin (MCW) is advancing an enterprise-wide transformation of clinical trial activation designed to reduce unnecessary delays, strengthen quality, improve transparency and accountability, and make it easier for investigators to bring promising studies to patients and research participants.

The Director, Clinical Trial Activation & Quality Office, provides senior operational leadership and strategic direction for the development, growth, and sustainability of the enterprise clinical trials portfolio. The Director will have a unique opportunity to oversee an integrated activation team and shape the systems, data, quality framework, and operating model that support MCW's growing clinical research portfolio.

The Director is a vital contributor and subject matter expert across the research mission, liaising with research leadership and the leadership of clinical partners to help steer strategic decision making, as well as developing strong partnerships with internal and external stakeholders as it relates to the operation and execution of efficient clinical trial activation and overall quality.

Reporting to the Assistant Dean, Research Operations, the Director serves as the primary operational advisor to Office of Research leadership on activation performance, quality, infrastructure, and emerging risks. The Director works across the Office of Research, academic departments, clinical partners, and other institutional functions to establish shared accountability, resolve barriers, and improve the end-to-end activation experience.

The Director leads the Activation and Quality Office, overseeing the clinical trials budget development team, managing infrastructure needs, and ensuring high-quality operations. The Director plays a critical role in measuring data-driven goals, ensuring standardization and transparency along the activation pipeline.

Primary Responsibilities
  • Lead MCW's centralized clinical trial activation function, creating an integrated, transparent, and accountable approach to advancing studies from initial intake and feasibility through budget, contract, regulatory, ancillary review, and activation, interfacing with other institutional units and partners providing activation support, such as Cancer Center, FT, and CW.

  • Direct program development, strategy, organizational development, long range planning, change management, and implementation of the infrastructure, processes and systems necessary to scale efficient, safe, and high-quality clinical trials at MCW.

  • Develop and monitor data-driven metrics to ensure efficient clinical trial activation, organizational transparency, stakeholder accountability, and opportunities for enhancement and improvement.

  • Analyze activation performance against institutional goals and national benchmarks to identify delays, recurring bottlenecks, variation across departments and study types, and opportunities for improvement; translate findings into recommendations for corrective action.

  • Identify, clarify, and resolve strategic impact issues with college wide impact which may span multiple areas, using advanced clinical trials and Good Clinical Practice knowledge requiring broad discretion and judgement.

  • In partnership with key stakeholders, assess and guide enterprise clinical trials infrastructure, including staffing levels, applications and software, and other items of organizational or fiscal impact.

  • Lead, develop, and mentor the Quality Office function; establish clear roles, service expectations, performance standards, and a culture of collaboration, accountability, continuous learning, and responsive support.

  • Oversee the operation of the centralized clinical trial budget development team,

  • Ensure ongoing compliance and adherence to quality standards and federal and institutional policies, monitoring and addressing issues and mitigating risks.

  • Participate on appropriate committees relevant to the advancement of the MCW clinical trials portfolio, and serve as a subject matter expert and liaison with institutional leaders, administration, faculty, other departments, affiliates, outside institutions, and national organizations.

  • Lead the continuous improvement of clinical research resources including workflows, tools, and SOPs with a focus on standardization, cost-effectiveness, productivity, and compliance.

  • Participate in and support internal and external meetings, site visits, and special events.

  • Other duties as assigned.

Knowledge - Skills - Abilities
  • Extensive experience with clinical research operations. Advanced working knowledge of study start-up activities (i.e., feasibility, budget development, contract negotiation and regulatory affairs)

  • Extensive experience in research program development. Superior organizational and change management skills. Advanced communication, presentation and negotiating skills.

  • Excellent management skills. Proven leadership, mentoring and supervisory skills. Ability to delegate tasks appropriately, influence behavior and drive performance.

  • Cultural awareness, customer focus, building trust, communication, critical thinking, and influencing skills are essential.

  • Proficient with use of research systems including OnCore Clinical Trials Management Software, TrialConnX, Epic, Florence eBinders, and other tools. Ability to understand system integrations and connectivity.

Qualifications

Appropriate experience may be substituted for education on an equivalent basis.

Minimum Required Education: Bachelor's degree

Minimum Required Experience: 10 years of clinical research operations management experience

Preferred Education: Masters Degree

Preferred Experience: Extensive experience in research program development and management. Extensive experience with clinical research operations. Research related activities at an academic medical center with clinical research activity. Recognized certification (e.g., ACRP or SOCRA) preferred.

Required Certification/Licensure(s): Certified Clinical Research Coordinator by ACRP or SOCRA preferred or must be obtained within 2 years of employment

Preferred Certification/Licensure(s):

Physical Requirements

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

Work Environment

Occasional exposure to dust, noise, temperature changes, or contact with water or other liquids. Work is performed in an environmentally controlled environment.

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.

#LI-AV1


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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