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Clinical Feasibility Jobs (NOW HIRING)

trinetx1

Senior Clinical Study Analyst

Cambridge, MA · On-site

Collaborate with the Clinical Feasibility & Analytics team and other Client Delivery staff on project evaluations, disease/study reports, and presentations * Document and escalate feedback on product ...

TriNetX, LLC

Senior Clinical Study Analyst

Cambridge, MA · On-site

$120 - $170/hr

Collaborate with the Clinical Feasibility & Analytics team and other Client Delivery staff on project evaluations, disease/study reports, and presentations * Document and escalate feedback on product ...

Medpace, Inc.

Feasibility Manager

Cincinnati, OH · On-site +1

By working cross functionally with our clinical operations, medical, commercial operations, and ... Conduct feasibility assessments for strategic or high priority clients in support of proposal ...

Medpace, Inc.

Feasibility Manager

Cincinnati, OH · On-site

By working cross functionally with our clinical operations, medical, commercial operations, and ... Conduct feasibility assessments for strategic or high priority clients in support of proposal ...

ObjectiveHealth

Feasibility Manager

Franklin, TN · On-site

Description Feasibility Manager The Feasibility Manager is responsible for leading the network ... This role sits at the intersection of clinical operations and business development, translating ...

New

ObjectiveHealth

Feasibility Manager

Franklin, TN · On-site +1

Feasibility Manager The Feasibility Manager is responsible for leading the network's response to ... This role sits at the intersection of clinical operations and business development, translating ...

Icon plc

Feasibility Informatics Manager

Hickory, NC · On-site

Feasibility Informatics Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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Feasibility Informatics Manager

Raleigh, NC · On-site

Feasibility Informatics Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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Feasibility Informatics Manager

Knoxville, TN · On-site

Feasibility Informatics Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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How much do clinical feasibility jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical feasibility in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What is clinical feasibility?

Clinical feasibility refers to the assessment process that determines whether a proposed clinical trial or study can be successfully conducted. This includes evaluating factors such as patient availability, site capabilities, regulatory requirements, budget, and timelines. The goal is to identify potential challenges early and ensure the study design is practical and achievable before full-scale implementation. Clinical feasibility helps reduce risks, save costs, and increase the likelihood of a successful clinical trial.

What are the key skills and qualifications needed to thrive in clinical feasibility?

To thrive in Clinical Feasibility, you need a solid background in clinical research, data analysis, and knowledge of regulatory guidelines, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), feasibility assessment tools, and databases like CT.gov is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital for collaborating with stakeholders and interpreting complex data. These skills ensure successful trial planning by accurately evaluating study viability, patient recruitment potential, and regulatory requirements.

What are some common challenges faced by professionals working in clinical feasibility roles, and how can they be addressed?

Professionals in Clinical Feasibility often encounter challenges such as accurately assessing patient recruitment potential, navigating complex regulatory landscapes across different regions, and integrating insights from diverse stakeholders. Addressing these challenges requires strong analytical skills, effective communication with clinical sites, and staying updated on regulatory requirements. Building collaborative relationships with investigators and leveraging data-driven tools can help improve feasibility assessments and ultimately increase the likelihood of successful study execution.

What is the difference between Clinical Feasibility vs Clinical Research Coordinator?

AspectClinical FeasibilityClinical Research Coordinator
Required CredentialsBachelor's degree, experience in clinical settingsBachelor's degree, experience in clinical trials
Work EnvironmentPre-study assessments, protocol evaluationsManaging trial activities, patient coordination
Employer & Industry UsagePharmaceutical companies, research institutionsHospitals, research centers, CROs

Clinical Feasibility specialists focus on assessing the practicality of conducting a clinical trial, including site capabilities and patient availability. Clinical Research Coordinators manage the day-to-day operations of clinical trials, ensuring protocol adherence and patient safety. While both roles require clinical knowledge, Clinical Feasibility emphasizes planning and assessment, whereas Clinical Research Coordinators handle trial execution.

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What cities are hiring for Clinical Feasibility jobs?

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What states have the most Clinical Feasibility jobs?

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What job categories do people searching Clinical Feasibility jobs look for?

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Clinical Feasibility jobs near you
Infographic showing various Clinical Feasibility job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.

Submission for the position: Supv Clinical Research - (Job Number: 26008816)

Baylor Scott & White Healthcare

Plano, TX • On-site

Full-time

Medical, Retirement, PTO

Re-posted 19 days ago

Baylor Scott & White Health rating

7.5

Company rating: 7.5 out of 10

Based on 773 frontline employees who took The Breakroom Quiz

232nd of 898 rated healthcare providers

Job description

About Us
Here at Baylor Scott & White Health we promote the well-being of all individuals, families, and communities. Baylor Scott and White is the largest not-for-profit healthcare system in Texas that empowers you to live well.
Our Core Values are:
  • We serve faithfully by doing what's right with a joyful heart.
  • We never settle by constantly striving for better.
  • We are in it together by supporting one another and those we serve.
  • We make an impact by taking initiative and delivering exceptional experience.
Benefits
Our benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include:
  • Immediate eligibility for health and welfare benefits
  • 401(k) savings plan with dollar-for-dollar match up to 5%
  • Tuition Reimbursement
  • PTO accrual beginning Day 1

Note: Benefits may vary based upon position type and/or level.
Job Summary
The Clinical Research Supervisor oversees daily supervision of Clinical Research staff. This position develops, negotiates, and monitors budgets for funded research projects. It also facilitates the implementation of clinical research projects and ensures quality and timely completion.
Essential Functions of the Role
  • Writes and assists in the development of proposals, grants, contracts, and budgets for the department.
  • Assists in developing new protocols and materials from study sponsors. Provides input to Principal Investigators and management on clinical and research issues to establish financial and clinical feasibility.
  • Assists various PIs, through delegated authority, in conducting clinical trials per federal, state, and institutional guidelines.
  • Prepares initial project submissions, amendment notifications, SAE reports, continuing review reports, and other reports for the IRB. Reviews staff-prepared submissions to ensure they meet established standards.
  • Oversees case report form completion by staff for all studies. Assists in coordinating audits by study sponsor monitors. Monitors assigned Clinical Research funds.
  • Orientates, trains, supervises, and evaluates Clinical Research staff. Encourages growth through complex responsibilities and education programs. Coordinates project assignments for staff.
  • Establishes and maintains good relations with the public, patients, and staff; promotes the department's research programs.
  • Monitors communication with the IRB, Food and Drug Administration (FDA), and other applicable regulatory agencies.
Key Success Factors
  • Research certification or other certifications per specialty area preferred.
  • Basic Life Support (BLS) per department requirements.
  • Proven written and oral communication skills.
  • Proven computer skills, including Microsoft Office, Excel, and PowerPoint.
  • Ability to manage time impressible projects in order to meet deadlines.
  • Ability to establish and maintain effective working relationships.
  • Excellent leadership skills.
Belonging Statement
We believe that all people should feel welcomed, valued and supported.
QUALIFICATIONS
  • EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification
  • EXPERIENCE - 2 Years of Experience

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