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Remote Clinical Operations Jobs in Kansas (NOW HIRING)

This is a 1 year remote-based contract position. What You'll Be Doing: * Serves as initial point of ... Monitors clinical operations metrics, activities and timelines on a regular basis; Tracks data ...

Your remit extends beyond clinical operations to encompass ICON's enterprise-wide Headcount ... LE1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the ...

... smooth trial operations. Your Profile: You will have a strong foundation in clinical trial ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

... smooth trial operations. Your Profile: You will have a strong foundation in clinical trial ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

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Showing results 1-20

Remote Clinical Operations information

See Kansas salary details

$31.2K

$87.4K

$166.3K

How much do remote clinical operations jobs pay per year?

As of Aug 28, 2026, the average yearly pay for remote clinical operations in Kansas is $87,436.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,700.00 and $101,200.00 per year, depending on experience, location, and employer.

What is a remote clinical operations?

A Remote Clinical Operations job involves overseeing and managing clinical trials and research activities from a remote location. Professionals in this role ensure studies comply with regulatory requirements, coordinate with cross-functional teams, and monitor trial progress. They work closely with investigators, sponsors, and site staff to ensure efficient trial execution. Strong organizational, communication, and problem-solving skills are essential for success in this position.

What are the typical day-to-day responsibilities of a remote clinical operations?

A Remote Clinical Operations professional is responsible for managing and monitoring clinical trial activities from a virtual office, which includes coordinating study timelines, communicating with clinical sites, and ensuring regulatory documentation is up to date. You may also be tasked with overseeing data quality, facilitating team meetings, and ensuring all trial processes adhere to protocols and compliance regulations. Most days involve frequent online collaboration with investigators, sponsors, and cross-functional teams, requiring strong virtual communication skills. The environment is typically dynamic, with priorities shifting based on project milestones and site needs, providing an engaging and varied work experience.

What are the key skills and qualifications needed to thrive in remote clinical operations, and why are they important?

To thrive as a Remote Clinical Operations professional, you typically need a background in clinical research or healthcare management, along with strong organizational and project management skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and industry regulations such as GCP and HIPAA is highly beneficial, and certifications like CCRA or CCRC are often preferred. Exceptional communication, time management, and problem-solving abilities help you collaborate effectively within remote and cross-functional teams. These competencies ensure seamless oversight of clinical trials and adherence to timelines and compliance standards when working remotely.

What are the most commonly searched types of Clinical Operations jobs in Kansas?

The most popular types of Clinical Operations jobs in Kansas are:

What are popular job titles related to Remote Clinical Operations jobs in Kansas?

For Remote Clinical Operations jobs in Kansas, the most frequently searched job titles are:

What cities in Kansas are hiring for Remote Clinical Operations jobs?

Cities in Kansas with the most Remote Clinical Operations job openings:

Infographic showing various Remote Clinical Operations job openings in Kansas as of August 2026, with employment types broken down into 56% Full Time, and 44% Part Time. Highlights an 100% Remote job distribution, with an average salary of $87,436 per year, or $42 per hour.

Clinical Lead II, Oncology (Contract)

Remote

Premier Research
Biotechnology Research and Development • 1 - 5K employees

Full-time

Posted 17 days ago


Job description

Premier Research is looking for a Clinical Lead II, Oncology (Contract) to join our Clinical Management team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

  • Your ideas influence the way we work, and your voice matters here.

  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

This is a 1 year remote-based contract position.

What You'll Be Doing:

  • Serves as initial point of contact for all site management and monitoring quality concerns, including initiation and oversight of site performance improvement plans (sPIP).

  • Plans, presents and participates in sponsor calls, representing Clinical and SSU function by providing status updates on clinical deliverables.

  • Oversees the quality of clinical monitoring, central monitoring and site management deliverables through the use of dashboards/reporting tools. Strong contributor to the central monitoring plan.

  • Monitors clinical operations metrics, activities and timelines on a regular basis; Tracks data entry timelines, open actions, protocol deviations, queries aging reports, SDR/SDV backlog and monitoring visit report turnaround timelines.

  • Ensures a state of audit readiness for both Premier and sites. Reviews/responds to audit findings and support sites in remediation/responses to any site audit findings.

  • Escalates through the established channels CRA/CM/SSU performance concerns, quality events, data breaches, serious breaches, scientific misconduct or any other event that requires prompt assessment and reporting.

What We Are Searching For:

  • Bachelor's degree, or its international equivalent from an accredited institution, in a clinical, biological, scientific, or health-related field; or equivalent work experience

  • 2 years of experience as a Clinical Lead. Prior onsite monitoring experience including experience with Risk-Based Monitoring is preferred.

  • Required Therapeutic Area: Oncology, with early phase experience preferred

  • Strong leadership skills including organizational skills, ability to persuade and motivate team members and sites to achieve targets.

  • Working knowledge of clinical financials including understanding of budgets, pass- through and resource management

  • Ability to multitask and work effectively in a fast-paced environment with changing priorities

Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status