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$89.7K

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How much do remote cra jobs pay per year?

As of May 31, 2026, the average yearly pay for remote cra in Renton, WA is $89,717.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,300.00 and $154,200.00 per year, depending on experience, location, and employer.

What Does a Remote CRA Do?

The responsibilities of a remote clinical research associate (CRA) involve working to monitor research efforts and progress. During a project, the remote CRA ensures that the research team follows all necessary protocols and procedures. In this career, your responsibilities also include maintaining records of relevant data and findings and monitoring the process of the project. Since this is a remote position, you perform your duties from home or another location away from the research site. When working on a clinical drug trial or medical study, you review procedures and ensure that researchers document all necessary information to meet regulatory requirements.

What are the key skills and qualifications needed to thrive as a Remote Clinical Research Associate (CRA), and why are they important?

To thrive as a Remote Clinical Research Associate, you need a solid background in life sciences or a related field, experience with clinical trials, and often a bachelor's degree or higher. Familiarity with electronic data capture (EDC) systems, regulatory compliance tools, and certifications such as ACRP or SOCRA are typically required. Exceptional organizational skills, attention to detail, and clear communication are essential soft skills for effective remote monitoring and collaboration. These skills are crucial to ensure protocol adherence, data integrity, and successful coordination of clinical studies from a remote setting.

What are some common challenges faced by Remote CRAs, and how can they be managed effectively?

Remote Clinical Research Associates (CRAs) often face challenges such as maintaining clear communication with on-site teams, managing multiple study sites virtually, and ensuring data integrity without in-person monitoring. To address these, successful CRAs leverage robust digital tools for documentation and communication, schedule regular virtual check-ins with site staff, and stay organized with meticulous tracking systems. Proactive problem-solving and adaptability are key to ensuring trial protocols are followed and regulatory requirements are met while working remotely.

What are Remote CRAs?

Remote Clinical Research Associates (CRAs) are professionals who monitor clinical trials and ensure compliance with regulatory requirements, study protocols, and data integrity, all while working from a remote location. Unlike traditional CRAs who travel to clinical sites, remote CRAs use technology to oversee site activities, review data, and communicate with site staff virtually. This role is essential in supporting the effective and efficient execution of clinical trials, especially as remote monitoring becomes more common in the industry.

What job makes $10,000 a month without a degree?

A remote customer service representative or sales professional can potentially earn $10,000 a month through commissions, bonuses, and high-volume work, especially in industries like tech or finance. Success typically requires strong communication skills, experience, and the ability to handle a high workload, often without formal degrees but with relevant training or certifications. Such roles may also involve flexible schedules and the use of customer relationship management (CRM) tools.

What is the difference between Remote Cra vs Remote Clinical Research Associate?

AspectRemote CraRemote Clinical Research Associate
CredentialsBachelor's degree in life sciences, clinical research experienceBachelor's degree, clinical trial knowledge, certification often preferred
Work EnvironmentHome-based, flexible schedules, virtual communicationPrimarily home-based, site visits may be required, virtual meetings common
Industry UsagePharmaceutical, biotech, CROsPharmaceutical companies, CROs, research organizations
Search & Comparison IntentYesYes

The Remote Cra and Remote Clinical Research Associate roles are similar in credentials, work environment, and industry usage. Both positions involve overseeing clinical trials remotely, requiring relevant education and experience. The main difference lies in terminology; 'Remote Cra' is often used interchangeably with 'Remote Clinical Research Associate,' but the latter may emphasize more formal certification and specific industry standards. Both roles are vital in advancing clinical research while offering flexible, remote work options.

More about Remote Cra jobs
What job categories do people searching Remote Cra jobs in Renton, WA look for? The top searched job categories for Remote Cra jobs in Renton, WA are:
What cities near Renton, WA are hiring for Remote Cra jobs? Cities near Renton, WA with the most Remote Cra job openings:
Remote Cra jobs near you

Clinical Research Associate

Kuros Biosciences, Inc.

Seattle, WA • On-site, Remote

$65K - $75K/yr

Full-time

Posted 19 days ago

Job description

The Clinical Research Associate (CRA) role focuses on supporting clinical trials, regulatory submissions, and ensuring compliance with relevant clinical regulations and industry standards. The primary responsibilities include managing study tracking tools, documentation, monitoring visits, and assisting in case of audits or inspections. This role also involves contributing to the efficient execution of clinical trials and the creation and distribution of scientific information related to Kuros Biosciences' products. Collaboration with the clinical team is essential for tasks such as ensuring compliance with protocols, reviewing clinical data, and supporting site staff.

The CRA will cover Washington, California, Utah, Illinois, Michigan and Texas and will oversee clinical research activities in these territories.

Key Responsibilities:

  • Oversee the management and tracking of clinical trial data to ensure accuracy, integrity, and completeness.

  • Conduct site qualification visits, site monitoring visits, and study close-out visits. Provide support to site staff during audits or inspections.

  • Ensure clinical trials are conducted in compliance with protocols, Good Clinical Practice (GCP), ICH guidelines, SOPs, and regulatory standards (FDA/DEA).

  • Review and manage electronic Case Report Forms (eCRFs), ensuring data is accurate and aligned with study protocols.

  • Assist in the development and maintenance of Case Report Forms (CRFs) and other study-related documents.

  • Provide training to site personnel on study procedures, protocols, and regulatory requirements.

  • Regularly review data entered into the Electronic Data Capture (EDC) system to ensure compliance with study protocols.

  • Identify, address, and escalate any study-related risks, issues, or opportunities for improvements.

  • Follow up with clinical sites to ensure that data collection is progressing as planned and all required documentation is completed.

  • Ensure timely and accurate management of regulatory documents and maintain compliance with regulatory requirements.

  • Engage with Key Opinion Leaders (KOLs) in the medical and research communities to stay informed on scientific research and clinical data.

  • Stay up-to-date with the latest developments in scientific research and clinical data relevant to Kuros Biosciences.

  • Review and track clinical trial-related invoices, ensuring accuracy and compliance.

  • Contribute to the creation and maintenance of project plans for clinical trials, ensuring alignment with company policies and timelines.

  • Work independently to complete tasks while ensuring alignment with team objectives, timelines, and expectations.

  • Expected to travel 5-7 days per month for site visits and clinical trial support.

Qualifications:

  • Organized, detail-oriented, with exceptional ability to manage timelines and deadlines.

  • Excellent communication and presentation creation skills.

  • Teamwork skills and an ability to work effectively in a cross-functional setting with a variety of colleagues.

  • Networking skills and the confidence to interact with senior experts, orthopaedic, and neurological surgeons.

  • Critical data analysis skills.

  • An ability to keep up to date with scientific literature.

  • Skilled at scientific and clinical writing.

  • A high level of emotional intelligence to work effectively with stakeholders.

  • The ability to understand, process, communicate, and present scientific information to a high standard.

  • External customer focus with strong networking capabilities and integration with KOLs.

  • Ability to manage multiple projects simultaneously and adapt priorities according to business and strategic needs.

  • Ability to work independently without immediate supervision (if remote).

Minimum Education and/or Experience Required:

  • Bachelor's Degree in a life sciences field (science-related discipline preferred).

  • Minimum 3 years of medical device industry experience.

  • Experience in conducting clinical trials, both as a sponsor and/or CRO, with on-site monitoring experience required.

  • The highest ethical standards, specifically surrounding protected medical information and clinical research.

  • Working knowledge of relevant clinical regulations and industry standards including Good Clinical Research Practice, ICH, ISO, FDA, and the MedTech EU Code of Practice.

  • Excellent verbal and written communication skills (protocols, reports, correspondence, etc.).

Pay Range
$65,000—$75,000 USD

Physical Requirements and Work Conditions

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.

  • Mobility & Posture: May require occasional sitting, standing, walking, climbing, reaching, bending, or stooping.
  • Lifting/Carrying: May require lifting and carrying items 50 pounds or more, depending on the role.
  • Manual Dexterity: Frequent use of hands and fingers for typing, writing, grasping, and operating office or job-specific equipment.
  • Driving: Some roles may require the ability to operate a motor vehicle for extended periods and maintain a valid driver's license.

Specific requirements may vary by role. Contact an HR representative for details related to the position.

Our credentials

Kuros is a Swiss-headquartered biotech company, listed on the SIX Swiss Stock Exchange since 2016 (under symbol KURN). With additional operations in the Netherlands and the USA, we continue to grow our global team.

To deliver the ideal bone graft, you need the highest quality and quantity of scientific evidence behind it. We believe that this is a key differentiator for Kuros, given the urgent need to advance bone healing.

  • Listing on the SIX Swiss Exchange under the symbol KURN since 2016
  • A commercial & research footprint that spans >20 markets
  • Dozens of clinical and scientific expert Advisers
  • >25 orthobiologics-related patents
  • >400 patients evaluated in Level I, randomized controlled clinical trials
  • >20 well-controlled Level I-IV clinical trials initiated, including 6 that are complete1
  • Published Level I evidence published in Spine

Kuros Biosciences is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Kuros Biosciences complies with GDPR and the California Consumer Privacy Act (CCPA). View our CCPA Notice here.