Conduct onsite / remote monitoring and complete related activities in accordance with study ... CRA or related profession in South Korea * Life science background * Excellent knowledge in KGCP ...
Conduct onsite / remote monitoring and complete related activities in accordance with study ... CRA or related profession in South Korea * Life science background * Excellent knowledge in KGCP ...
Remote Cra information
See Maine salary details
$10.7K - $21.8K
0% of jobs
$27.3K is the 25th percentile. Wages below this are outliers.
$21.8K - $32.9K
51% of jobs
$32.9K - $44.1K
13% of jobs
$44.1K - $55.2K
0% of jobs
$55.2K - $66.3K
0% of jobs
$66.3K - $77.5K
0% of jobs
$77.5K - $88.6K
0% of jobs
$88.6K - $99.7K
0% of jobs
$99.7K - $110.9K
0% of jobs
$110.9K - $122K
0% of jobs
$125.5K is the 75th percentile. Wages above this are outliers.
$122K - $133.1K
36% of jobs
$10.7K
$76.9K
$133.1K
How much do remote cra jobs pay per year?
What is a remote CRA?
What are the key skills and qualifications needed to thrive as a remote CRA, and why are they important?
What is the difference between Remote Cra vs Remote Clinical Research Associate?
| Aspect | Remote Cra | Remote Clinical Research Associate |
|---|---|---|
| Credentials | Bachelor's degree in life sciences, clinical research experience | Bachelor's degree, clinical trial knowledge, certification often preferred |
| Work Environment | Home-based, flexible schedules, virtual communication | Primarily home-based, site visits may be required, virtual meetings common |
| Industry Usage | Pharmaceutical, biotech, CROs | Pharmaceutical companies, CROs, research organizations |
| Search & Comparison Intent | Yes | Yes |
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.
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 some common challenges faced by remote CRAs, and how can they be managed effectively?

Clinical Research Associate II or higher for our Korean Office
Grand Lake Stream, ME • On-site, Remote
Full-time
Re-posted yesterday
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