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NorthWest Arkansas Community College

AR · On-site

$2.48K/wk

NorthWest Arkansas Community College is seeking qualified applicants to establish a pool for part-time and/or substitute instructors in the Certified Retail Analyst (CRA) certification program.

Nwacc

AR · On-site

$2.48K/wk

NorthWest Arkansas Community College is seeking qualified applicants to establish a pool for part-time and/or substitute instructors in the Certified Retail Analyst (CRA) certification program.

Thermo Fisher Scientific

Clear development pathways (e.g., Senior CRA, Lead CRA, CTM) * Flexible working models that support ... Permanent employment * Full-time (40 hours/week) or Part-time (32 hours/week) options available ...

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How much do part time cra jobs pay per hour?

As of May 29, 2026, the average hourly pay for part time 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 Part Time CRA job?

A Part-Time Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory guidelines, protocols, and good clinical practices. They typically work on a reduced schedule while overseeing site activities, ensuring data accuracy, and maintaining communication with investigators. Part-time CRAs may be employed by pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This role is ideal for professionals seeking flexibility while contributing to the success of clinical research.

What are the key skills and qualifications needed to thrive in the Part Time Cra position, and why are they important?

To thrive as a Part Time CRA (Clinical Research Associate), you need a background in life sciences or a related field, an understanding of clinical trial processes, and prior experience in clinical research. Familiarity with electronic data capture systems, Good Clinical Practice (GCP) certification, and knowledge of regulatory guidelines are often required. Excellent organizational, communication, and problem-solving skills help with managing multiple study sites and working independently. These competencies are crucial for ensuring clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards.

What does a typical work week look like for a Part Time CRA?

A typical work week for a Part Time CRA may include monitoring study sites remotely or in person, reviewing trial documentation, ensuring regulatory compliance, and communicating updates to site staff and sponsors. You may also be responsible for verifying data accuracy, assisting with site training, and resolving any study-related issues that arise. The workload can vary depending on the stage of the clinical trial and the number of assigned sites, but flexibility and effective time management are essential. Team collaboration is common, as you'll coordinate closely with investigators, research coordinators, and project managers to ensure smooth trial operations.

Is CRA a good career?

A CRA (Clinical Research Associate) is a role in the healthcare and pharmaceutical industries responsible for monitoring clinical trials to ensure compliance and data integrity. It offers opportunities for career growth, requires attention to detail, and often involves travel and certification such as the CCRP. Whether it is a good career depends on individual interests in research, science, and regulatory processes.
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Infographic showing various Part Time Cra job openings in the United States as of May 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $85,542 per year, or $41.1 per hour.
Clinical Research Associate - Part Time

Clinical Research Associate - Part Time

CND Life Sciences

Scottsdale, AZ • On-site

$36.54/hr

Part-time

Posted 7 days ago

Job description

Description
The Clinical Research Associate (CRA) is responsible for overseeing and monitoring clinical trials conducted at CND's internal site and investigator sites sponsored by CND or in collaboration with external partners. This role ensures that studies are executed in compliance with study protocols, Good Clinical Practice (GCP) guidelines, budget constraints, and established milestone timelines. The CRA must have a strong understanding of clinical trial methodologies, regulatory requirements, and the ability to collaborate effectively with the investigators and internal and external cross-functional teams. The CRA consistently upholds the highest standards of professionalism.
Job Responsibilities
  • Regulatory Compliance: Ensure all clinical trials are conducted in adherence to the study protocol, ICH-GCP guidelines, relevant regulations and SOPs. Manage central IRB tasks for participating sites from start-up through close-out.
  • CND Site Subject Visits: Assist providers with subject recruitment, scheduling and conducting site visits at the internal CND site as needed. Responsibilities may include obtaining informed consent (ICF), assessing inclusion/exclusion criteria, recording vitals, and performing blood draws.
  • Site Initiation: Conduct site initiation visits remotely or in person to assess site readiness, including regulatory start-up, facility reviews, annual bio-calibrations, supply storage, staff qualifications and training, study procedures and data entry management. Ensure all required site documents are collected and tracked in compliance with regulatory requirements and internal Standard Operating Procedures (SOPs). May also involve updating clinicaltrials.gov with site-specific information.
  • Study Monitoring: Perform regular site monitoring visits remotely (via eCRF) or in person (via site source documents) per study-specific monitoring plans and timelines. Oversee data entry, protocol adherence, query resolution, quality compliance, and patient safety reporting, escalating protocol deviations or subject safety concerns as needed. Assist in the development of study-specific monitoring plans.
  • Site Communication: Maintain proactive communication with site staff, responding to inquiries timely and escalating urgent matters as necessary.
  • Site Engagement and Subject Recruitment: Monitoring weekly site recruitment logs to verify subject eligibility and enrollment. Assist sites with IRB approvals for advertising and recruitment strategies. Support community patient advocacy outreach when needed.
  • Site Invoices: Review and approve site invoices based on completed EDC data entry and query resolution for all subject visits invoiced, including start-up and close-out visits.
  • Data Management: Oversee the collection, processing, and documentation of study data. Ensure data integrity through thorough data review and timely query resolution following study-specific monitoring plan milestones.
  • Safety Reporting: Oversee the reporting of adverse events and serious adverse events, ensuring compliance with regulatory requirements.
  • Site Close-Out: Conduct site close-out activities to ensure proper data lock, storage, and archiving study documents.
  • Trial Documentation: Maintain and manage all clinical trial documents, ensuring they remain current and compliant with regulatory standards.
  • Team Collaboration: Work closely with internal and external cross-functional teams and vendors to ensure clinical trials are executed efficiently, within budget and in alignment with study milestones.
  • Reporting: Provide regular updates and comprehensive reports to the Senior Director of Clinical Research and/or designated CR lead and other stakeholders on trial progress.
  • Quality Assurance and Compliance Participate in internal and external audits, addressing findings, and implement corrective and preventive actions as necessary.
  • Perform other duties as assigned.

Knowledge, Skills & Experience
  • Minimum of 5 years of clinical research experience as a Clinical Research Coordinator or at least 2 years of experience as a Clinical Research Associate.
  • Therapeutic experience in neurology is highly preferred.
  • Experience in Phase I, II or III of clinical trials; familiarity with NIH and other government-sponsored protocols a plus.
  • In-depth knowledge of ICH-GCP guidelines and relevant regulatory requirements for clinical trial conduct.
  • Strong proficiency in IT tools including the MS 365 suite, Electronic Data Capture (EDC) systems, Clinical Trial Management Systems (CTMS) and other applicable technologies.
  • Excellent written and verbal communication skills.
  • Strong multitasking skills, attention to detail, creative problem-solving, and the ability to maintain accurate records.
  • Demonstratedability to identify and resolve site-related challenges with strong negotiation skills.
  • Proven ability to work effectively in a team-based environment.
  • Willingness and ability to travel to clinical sites as needed.

Education, Certifications, and Licensures
  • Bachelor's of Science degree or related field required.
  • The Collaborative Institutional Training Initiative (CITI) Good Clinical Practice (GCP) certification, or its equivalent, or willing to complete within first month of hire.
  • International Air Transport Association (IATA) certification, if indicated

Other
  • Combination of seated and standing work to complete the core functions of the role
  • Sit and stand for long periods of time
  • Visual acuity and analytical skills
  • This job will be expected to work onsite at CND's Scottsdale, AZ headquarters 3-5 days/week

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