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Contract Cra Jobs in Wisconsin (NOW HIRING)

WI · On-site

$79.09 - $93/hr

By managing complex contracts and financial operations with precision, the role supports clinical research that advances patient care and scientific innovation. Employees with CRA certification are ...

The Sr. CRA provides guidance to less experienced CRAs, supports investigator sites, proactively ... Provide mentoring, training, and functional oversight of CRAs, including contingent (contract) CRAs.

The Sr. CRA provides guidance to less experienced CRAs, supports investigator sites, proactively ... Provide mentoring, training, and functional oversight of CRAs, including contingent (contract) CRAs.

The Sr. CRA provides guidance to less experienced CRAs, supports investigator sites, proactively ... Provide mentoring, training, and functional oversight of CRAs, including contingent (contract) CRAs.

WI · On-site

$79 - $93/hr

Employees with CRA certification are eligible for certification pay. The role is eligible for a ... Communicates with BCM Accounting, Grants & Contracts, and collaborating institutions to ensure sub ...

Contract Cra information

See Wisconsin salary details

$12

$41

$70

How much do contract cra jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for contract cra in Wisconsin is $41.51, according to ZipRecruiter salary data. Most workers in this role earn between $29.13 and $53.12 per hour, depending on experience, location, and employer.

What is a contract CRA?

A contract clinical research associate (contract CRA) is a temporary position in which you manage clinical trials and scientific research projects. As a contractor, you work temporarily on a contract that typically lasts for the duration of the project. Clinical research associates work in the pharmaceutical industry to ensure the safety and effectiveness of medication or vaccines. You can also work on studies for biotech companies and projects that perform analysis on surgical procedures or treatments. Your duties focus on planning the trial, defining the parameters, ensuring the safety of participants, and making sure the project meets all regulations and requirements.

What are the key skills and qualifications needed to thrive as a contract CRA, and why are they important?

To thrive as a Contract CRA, you need a solid understanding of clinical research protocols, regulatory guidelines (like GCP/ICH), and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like ACRP or SOCRA are beneficial. Strong attention to detail, excellent organizational skills, and effective communication are crucial soft skills for managing multiple studies and collaborating with sites. These competencies are essential for ensuring compliance, data integrity, and the smooth execution of clinical trials.

What are some common challenges faced by contract CRAs and how can they effectively manage them?

Contract CRAs often juggle multiple clinical trial sites and studies, which can make prioritizing and time management especially challenging. They must adapt quickly to each sponsor's protocols and systems, often with limited onboarding. Building strong relationships with site staff and maintaining clear, consistent communication are key to overcoming these challenges. Staying organized through meticulous documentation and leveraging digital tools can help contract CRAs efficiently meet monitoring visit deadlines and regulatory requirements.

What are the most commonly searched types of Cra jobs in Wisconsin?

The most popular types of Cra jobs in Wisconsin are:

What are popular job titles related to Contract Cra jobs in Wisconsin?

For Contract Cra jobs in Wisconsin, the most frequently searched job titles are:

Infographic showing various Contract Cra job openings in Wisconsin as of August 2026, with employment types broken down into 94% Full Time, 4% Part Time, and 2% Contract. Highlights an 77% Physical, 6% Hybrid, and 17% Remote job distribution, with an average salary of $86,342 per year, or $41.5 per hour.

Senior Research Administration Associate - Clinical Trial Billing and Finance

Baylor College of Medicine

WI • On-site

$79.09 - $93/hr

Other

Posted 4 days ago


Baylor College of Medicine rating

8.0

Company rating: 8.0 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

190th of 630 rated colleges and universities


Job description

Senior Research Administration Associate - Clinical Trial Billing and Finance

  • Division: Pediatrics
  • Work Arrangement: Hybrid
  • Location: Hybrid within Greater Houston, TX
  • Salary Range: $79,092 - $93,000
  • FLSA Status: Exempt
  • Work Schedule: Monday – Friday, 8 a.m. – 5 p.m.
Summary

The Senior Research Administration Associate – Clinical Trial Billing and Finance is a pivotal role responsible for managing the financial lifecycle of industry-sponsored clinical trials in the Center of Research Advancement for the Departments of Pediatrics and other supported TCH Departments. This position ensures accurate and compliant handling of all financial activities, primarily post-award responsibilities such as invoicing, payment tracking, account reconciliation, and financial reporting. The position acts as a critical link between investigators, sponsors, and internal teams to ensure compliance with institutional and federal regulations while maintaining financial accuracy and transparency. By managing complex contracts and financial operations with precision, the role supports clinical research that advances patient care and scientific innovation.

Employees with CRA certification are eligible for certification pay.

The role is eligible for a hybrid work arrangement after completing onboarding and training onsite (typically about 6 months). Employees working a hybrid schedule may be asked to attend in-person meetings and trainings.

Job Duties

POST-AWARD FINANCIAL MANAGEMENT

  • Oversee financial activities for active clinical trials, including expense tracking and account reconciliation.
  • Prepare and submit invoices for protocol-related items, study visits, pass-through costs, and patient-related expenses.
  • Manage internal invoices for staff time and effort allocation.
  • Track billed invoices, follow up with sponsors, and record payments in CTMS Finance Module.
  • Prepare financial reports for CRA, Department leaders and stakeholders.

REPORTING AND COMPLIANCE

  • Generate monthly financial reports using SAP, BRAIN, CTMS, and contract tracking systems.
  • Review research expenditures for accuracy prior to sponsor billing.
  • Maintain budget data in CTMS and ensure compliance with billing policies and federal regulations.
  • Assist in developing and maintaining SOPs and procedural guidelines.

STUDY CLOSE OUT

  • Evaluate study trials for financial closure and perform comprehensive final billing reconciliation.
  • Review contract terms and Principal Investigator agreements to ensure all financial obligations, deliverables, and compliance requirements are met prior to study closure.

PRE-AWARD ACTIVITIES

  • Conduct coverage analysis and cost assessments.
  • Develop and negotiate study budgets.
  • Support financial setup and resource allocation for new studies.
  • Participate in study feasibility and related meetings, providing expertise in budgeting and financial management to ensure accurate cost projections and compliance with institutional and sponsor requirements.
  • Serve as the primary point of contact for budget development, ensuring alignment with study requirements and facilitating efficient study execution and accurate billing processes.

OTHER DUTIES

  • Participate in process improvement initiatives.
  • Perform other job-related duties as assigned.
Minimum Qualifications
  • Bachelor's degree. Certified Research Administrator certification through the Research Administrators Certification Council (RACC) may substitute for the degree requirement.
  • Four years of relevant experience.
Department Specific Criteria
  • Direct experience in clinical trial billing and account reconciliation.
  • Prior experience in an academic or clinical research setting.
  • Familiarity with accounting principles and pre-/post-award management.
  • Strong attention to detail and data integrity.
  • Ability to interpret and manage complex research contracts.
  • Excellent communication skills for internal and external stakeholders.

Work Authorization Requirement:

This position is not eligible for visa sponsorship.

Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.

Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.

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