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Solomon Page

Contract CRA

Covington, KY · On-site

$90 - $100/hr

We are seeking an experienced and highly motivated Clinical Research Associate (CRA) to support a ... Contract Duration: 6 Months with Possibility of Extension * Start Date: ASAP * Therapeutic Area:

Solomon Page

Contract CRA

Covington, KY · On-site

$90 - $100/hr

Contract Duration: 6 Months with Possibility of Extension * Start Date: ASAP * Therapeutic Area ... Minimum 5 years of Clinical Research Associate (CRA) experience. * Direct monitoring experience in ...

Alira Health

Assists in set up/collection of site specific ethics documents and site contract negotiation as ... Performs CRA mentoring. * Collaborates with development and maintenance of Clinical Trial ...

Alira Health

Clinical Research Associate CRA

Assists in set up/collection of site specific ethics documents and site contract negotiation as ... Performs CRA mentoring. * Collaborates with development and maintenance of Clinical Trial ...

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How much do contract cra jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for contract cra in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 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.
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Contract CRA jobs near you
Infographic showing various Contract Cra job openings in the United States as of August 2026, with employment types broken down into 96% Full Time, 2% Part Time, and 2% Contract. Highlights an 77% Physical, 6% Hybrid, and 17% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Contract CRA

Solomon Page

Covington, KY • On-site

$90 - $100/hr

Contractor

Medical, Dental, Vision, Retirement

Re-posted 29 days ago

Job description

We are seeking an experienced and highly motivated Clinical Research Associate (CRA) to support a Phase 3 clinical trial in the Kidney transplant therapeutic area. The ideal candidate will have a strong background in site monitoring and clinical trial management, with direct experience supporting pulmonary or transplant studies. This is a home-based position for a CRA located in the Midwest/Central U.S. region, with regular travel to assigned investigative sites across the United States.
  • Location: Midwest/Central United States (Home-Based)
  • Employment Type: 1.0 FTE Contract
  • Contract Duration: 6 Months with Possibility of Extension
  • Start Date: ASAP
  • Therapeutic Area: Kidney Transplant
  • Clinical Trial Phase: Phase III
  • Pay Rate: $90-100/hr
Required Qualifications:
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
  • Minimum 5 years of Clinical Research Associate (CRA) experience.
  • Direct monitoring experience in kidney transplant and/or kidney transplant clinical studies is required.
  • Strong understanding of ICH-GCP, FDA regulations, and clinical trial processes.
  • Experience managing high-performing academic medical center sites.
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to travel regularly to assigned study sites.
Clinical Resource Network Distinction
CRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
About CRN
Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn .
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