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Remote Cra Pharmaceutical Jobs (NOW HIRING)

Vanguard Clinical

Clinical Research Associate (Pool)

CA · Remote

$90K - $130K/yr

This position is available for remote work in the following states: AZ, CA, CO, CT, FL, GA, KS, MA ... The Clinical Research Associate (CRA) will execute monitoring responsibilities for clinical trials ...

Medasource

Sr. CRA

Minneapolis, MN · Remote

Remote with Travel required (North Central Region) Duration: 12 Month Contract with the possibility ... Experience in a medical device/pharmaceutical company or clinical/hospital environment (preferred)

Immatics NV

Senior Clinical Research Associate

$120K - $135K/yr

The Senior CRA will be responsible for overseeing clinical trial site management and monitoring ... Fully Remote Salary Range: $120,000 to $135,000 Basic Qualifications: * Bachelor's degree in life ...

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Remote Cra Pharmaceutical information

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$11K

$79.4K

$137.5K

How much do remote cra pharmaceutical jobs pay per year?

As of Jun 14, 2026, the average yearly pay for remote cra pharmaceutical in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

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

To thrive as a Remote CRA in the pharmaceutical industry, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP), and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and certifications like ACRP or SOCRA are commonly required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills help you excel in a remote environment and coordinate effectively with trial sites. These skills and qualifications are crucial to ensure compliance, data integrity, and the smooth execution of clinical studies across geographically dispersed sites.

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

AspectRemote Cra PharmaceuticalRemote Clinical Research Associate
CertificationsTypically requires GCP training, CRA certificationRequires GCP training, CRA certification
Work EnvironmentPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms
Industry UsageCommon in pharma and biotech sectorsCommon in clinical trial management across industries
Job FocusMonitoring clinical trials for pharmaceutical productsMonitoring and managing clinical trial sites

The Remote Cra Pharmaceutical and Remote Clinical Research Associate roles are closely related, both requiring similar certifications and working within the pharmaceutical and biotech industries. The main difference lies in the job focus: Remote Cra Pharmaceutical often emphasizes overseeing drug development processes, while Remote Clinical Research Associate primarily manages clinical trial sites and data collection. Both roles are vital in advancing new therapies and are frequently sought after by companies conducting clinical research remotely.

What are some common challenges faced by a Remote CRA (Clinical Research Associate) in the pharmaceutical industry, and how can they be managed?

As a Remote CRA in the pharmaceutical field, one of the key challenges is maintaining effective communication and oversight with clinical trial sites without frequent in-person visits. This can make it more difficult to build rapport, monitor compliance, and resolve site issues promptly. To manage these challenges, CRAs often rely on robust digital tools, regular virtual meetings, and clear documentation practices. Staying organized, being proactive in follow-up, and fostering strong remote relationships with site staff are essential for ensuring trial integrity and smooth study progress.

What is a Remote CRA in the pharmaceutical industry?

A Remote Clinical Research Associate (CRA) in the pharmaceutical industry is responsible for monitoring clinical trials and ensuring compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements, but they perform these duties remotely rather than through frequent on-site visits. Remote CRAs review study data, communicate with clinical sites, and support the trial process using digital tools and platforms. This role enables organizations to conduct high-quality clinical research while reducing travel and increasing efficiency, especially in decentralized or multi-site studies.
More about Remote Cra Pharmaceutical jobs
What cities are hiring for Remote Cra Pharmaceutical jobs? Cities with the most Remote Cra Pharmaceutical job openings:
What are the most commonly searched types of Cra Pharmaceutical jobs? The most popular types of Cra Pharmaceutical jobs are:
What states have the most Remote Cra Pharmaceutical jobs? States with the most job openings for Remote Cra Pharmaceutical jobs include:
What job categories do people searching Remote Cra Pharmaceutical jobs look for? The top searched job categories for Remote Cra Pharmaceutical jobs are:
Remote Cra Pharmaceutical jobs near you
Infographic showing various Remote Cra Pharmaceutical job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate II or higher for our Korean Office

CTI

Grand Lake Stream, ME • On-site, Remote

Full-time

Posted 4 days ago

Job description

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

What You’ll Do

  • Serve as main CTI contact for assigned study sites
  • Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP
  • Conduct or assist with study start-up activities, including feasibility, pre-study activities and site selection
  • Collect, review and track essential/regulatory documents
  • Participate in and complete all general and study specific training as required
  • Participate in investigator, client and project team meetings; may include presentations
  • Create and implement subject enrollment strategies for assigned study sites
  • Ensure proper storage, dispensation and accountability of all Investigational Product (IP) and trial-related materials
  • Perform site management activities and provide ongoing updates of site status to Clinical Project Manager
  • Conduct onsite / remote monitoring and complete related activities in accordance with study specific Monitoring Plan
  • Utilize systems and reports to track subject status, subject case report form (CRF) retrieval / source document review (SDV), regulatory documents, and IP
  • Assist with project-specific activities as member of Project Team

What You Bring

  • 2-5 years clinical research experience as a CRA or related profession in South Korea
  • Life science background
  • Excellent knowledge in KGCP, ICH-GCP and regulatory requirements
  • Experience in Oncology or Transplant is a plus
  • Fluent (Level B2 to C1) in spoken and written language in Korean and in English
  • You need to be fully eligible to work in Korea. CTI does not offer any Sponsorship

 

Why CTI?

At CTI, we recognize that our people are what make our company successful. Our work moves medicine forward.

  • Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through a dedicated training department.
  • Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering hybrid work from home opportunities. We also encourage care for the world around us through our unique CTI Cares program.
  • Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market. 

Important Note
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note

  • We will never communicate with you via Microsoft Teams or text message
  • We will never ask for your bank account information at any point during the recruitment process

Apply