ZipRecruiter

Log In

2

Remote Cra Jobs in Kentucky (NOW HIRING)

CTI

Clinical Trial Manager

Covington, KY · On-site +1

... CRA Line Manager * May serve as a contact/resource for investigative sites as required * May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre-study and ...

CTI

Clinical Trial Manager

Covington, KY · Remote

... CRA Line Manager * May serve as a contact/resource for investigative sites as required * May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre-study and ...

All JobsCra JobsRemote Cra JobsRemote Cra Jobs in Kentucky

Remote Cra information

See Kentucky salary details

$9.6K

$69K

$119.4K

How much do remote cra jobs pay per year?

As of Aug 9, 2026, the average yearly pay for remote cra in Kentucky is $68,993.00, according to ZipRecruiter salary data. Most workers in this role earn between $28,700.00 and $118,600.00 per year, depending on experience, location, and employer.

What is a remote CRA?

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 are the key skills and qualifications needed to thrive as a remote 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 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.

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?

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.
More about Remote Cra jobs
What are the most commonly searched types of Cra jobs in Kentucky? The most popular types of Cra jobs in Kentucky are:
What are popular job titles related to Remote Cra jobs in Kentucky? For Remote Cra jobs in Kentucky, the most frequently searched job titles are:
What job categories do people searching Remote Cra jobs in Kentucky look for? The top searched job categories for Remote Cra jobs in Kentucky are:
What cities in Kentucky are hiring for Remote Cra jobs? Cities in Kentucky with the most Remote Cra job openings:
Remote Cra jobs near you
Infographic showing various Remote Cra job openings in Kentucky as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $68,993 per year, or $33.2 per hour.

Clinical Trial Manager

CTI

Covington, KY • On-site, Remote

Full-time

Posted 23 days ago

Job description

What You'll Do
  • Review scope of project and resourcing related to Clinical Monitoring with Clinical Project Management
  • Plan, schedule, and implement the clinical monitoring aspects of projects
  • Define and implement project-specific functional standards, goals, and expectations with Clinical Monitoring team including KPIs, KRIs, QTLs and additional metrics as agreed upon
  • Primary point of contact for Clinical Monitoring aspects of designated projects
  • Serve as advocate for the Clinical Monitoring team with the client
  • Coordinate and oversee daily operations of Clinical Monitoring team, including CRAs and in-house personnel. Ensure assigned CRAs receive therapeutic and project-specific training
  • Develop CRA tools and CRA training materials
  • Organize and conduct CRA meetings/calls if in project scope
  • Ensure accurate tracking of any relevant study information related to Clinical Monitoring deliverables
  • Oversight of key clinical monitoring metrics, including but not limited to: Visits scheduled per CTMP, Monitoring Visit Reports (MVR) and associated correspondence timelines, Action Items (AI), query resolution, and other quality metrics, to ensure they are met and followed-up on as necessary
  • Provide oversight of visit report review and approval, including site issue escalation and resolution; may conduct visit report review and approval depending on team structure
  • Manage clinical monitoring related project milestones and proactively address deficiencies
  • Oversee the quality and timeliness of clinical data in the eDC per Clinical Trial Monitoring Plan
  • Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and maintained in accordance with SOPs
  • Active involvement in clinical monitoring risk planning and assessment, developing mitigation strategies and associated action plans, issue escalation, and resolution
  • Ensure all clinical monitoring/site management related closeout activities are completed
  • Mentor CRAs, as needed, on the Clinical Project team to ensure high performance and productivity
  • Provide feedback/information on CRA performance as requested by CRA line managers
  • As necessary serve as CRA trainer/mentor and accompany CRAs in the field for training visits, assessment/oversight visits, or co-monitoring visits.
  • Develop successful cross-functional relationships with internal and external team members.
  • May be required to undertake specific CPM tasks, as agreed with Line Manager
  • Ability to understand and oversee CRA timesheets for tracked hours exceeding budgeted hours and escalate to CPM and CRA Line Manager
  • May serve as a contact/resource for investigative sites as required
  • May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre-study and Site Initiation Visits during project startup
  • May act as the primary monitoring point of contact for sponsors and sites for smaller or single service projects
  • Participate in Bid Defense planning and Bid Defense Meetings as requested
  • Assist with other duties as assigned

What You'll Bring
  • Excellent verbal and written communication skills
  • Excellent organizational and time management skills
  • Excellent critical thinking and decision-making skills; proactively identify challenges and potential risks
  • Excellent collaboration, customer service, and interpersonal skills
  • Ability to work independently
  • Proficient in use of laptop computer and software systems, including Clinical Trial Management (CTMS), electronic Trial Master File (eTMF), Electronic Data Capture (EDC), Microsoft Excel/PowerPoint/Word, or similar systems
  • Ability to understand complex medical terminology and procedures
  • Ability to review and explain study budgets to CRA and CMAs
  • Ability to monitor complex indications
  • Expert knowledge of ICH/GCP and all applicable regulatory requirements
  • Ability to mentor and provide constructive feedback to lesser experienced
  • At least 8 years as CRA or other experience in clinical research deemed pertinent by hiring manager
  • Prior proficient performance as Lead CRA for at least 1 year
  • Maintained previous role performance KPIs and metrics at fully performing or exceeds level for at least 2 years
  • Demonstrated successful performance at Senior CRA level, with at least 4 of the required 8 years as CRA, of experience monitoring complex studies
  • Bachelor's Degree or higher in allied health field such as nursing, pharmacy, or health / natural science, or RN with Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing experience, or equivalent experience as determined by CTI Management and Human Resources
  • Experience in conducting clinical research studies in hospital setting, pharmaceutical company or CRO

Why CTI?
  • We support career progression - 25% of our global staff is promoted annually and we have a structured mentoring program to provide the support you need to move forward
  • We value education and training - We provide tuition reimbursement, partner with universities and colleges to create programs in our field, and have a dedicated training department
  • We value our people - We have never had a layoff in our 20-year history, support a work-life balance with flexible schedules, and have provided cash bonuses every year for the past decade
  • Our culture is unparalleled - Click here to learn more about "The CTI Way"
  • We think globally and act locally - We have a global philanthropic program supporting our team's efforts to improve their local communities (Click here to learn more about our "CTI Cares" program)

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

Equal Opportunity Employer/Veterans/Disabled
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

Apply