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Clinical Feasibility Jobs (NOW HIRING)

TriNetX LLC

Senior Clinical Study Analyst

Cambridge, MA · On-site

$85K - $95K/yr

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 ...

trinetx1

Senior Clinical Study Analyst

Cambridge, MA

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 ...

ICON

Feasibility Informatics Manager

Center Square, PA · On-site

$110 - $160/hr

To lead the process of clinical project feasibility during standalone feasibility (awarded) projects by managing and being accountable for the delivery of all awarded projects assigned to the ...

CenExel

Feasibility Manager

CenExel is a leading nationwide clinical research site and patient network serving the life ... Tracks and manages the early and/or late phase feasibility process, maintaining storage of ...

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 ...

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 ...

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Clinical Feasibility information

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How much do clinical feasibility jobs pay per hour?

As of Aug 14, 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 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 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 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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Cities with the most Clinical Feasibility job openings:

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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, 72% Full Time, 17% 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.

Senior Clinical Study Analyst

TriNetX LLC

Cambridge, MA • On-site

$85K - $95K/yr

Full-time

Posted 13 days ago

Job description

POSITION TITLE: Sr. Clinical Study Analyst
LOCATION: Cambridge, MA (hybrid) OR U.S. remote
This position reports to our global HQ in Cambridge, MA. Travel is expected domestically and internationally when needed.
Who We Are:TriNetX connects healthcare organizations and researchers across the globe so they can see what's happening in real patient populations-not guesses, not simulations.
Our aim is simple and ambitious: Provide a clear path to trustworthy answers, whether your goal is to create promising new therapies, publish groundbreaking research, or improve health outcomes.
We keep identifiable data where it belongs-inside more than 11,000+ clinical sites across 20+ countries-preserving security, provenance, and granularity. Our trusted partnerships with providers ensure high-fidelity data, and a properly governed linkage back to individual patients.
At TriNetX, we enable life sciences, healthcare, and academic institutions to strengthen human health-with data you can trace, evidence you can defend, and answers you can trust.
Who We Are Looking For:
The Sr. Clinical Study Analyst will need to draw upon their extensive expertise across the areas of clinical research and clinical trial design and execution to help our customers meet their goals. This role will support and educate users in a consultative manner, ultimately creating self-sufficient users of our platform and driving product adoption in the process. The ideal candidate is someone willing to learn our platform, data, and tools while utilizing existing clinical information and skills to discover new approaches in solving challenging matters.
What You Will Be Doing:
  • Independently translate eligibility criteria and query for patient cohorts using TriNetX LIVE™
  • Apply standard coding schemes (ICD, CPT, SNOMED, etc.) to define patient cohorts based on provided criteria
  • Deeply understand nuances of clinical trial eligibility criteria and represent them using available clinical data sources
  • Lead live demos and training sessions to existing and prospective users of TriNetX LIVE™ with minimal oversight
  • Serve as primary contact for pharma, biotech, CRO, and healthcare organization clients to identify, analyze and interpret data relevant to clinical questions and needs, and provide consultative assistance via written, oral, or in-person presentation methods
  • Handle a high volume and complexity of daily questions from pharma and healthcare organization users regarding platform and analytic capabilities
  • Manage multiple simultaneous customer engagements using effective workload management and prioritization capabilities
  • 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 usability and potential new features to senior team members
  • Support the sales and training processes of TriNetX on both the healthcare organization and sponsor (pharma/CRO) user ends of the platform
  • Participate in and lead team meetings, training sessions, and knowledge-sharing initiatives to build expertise in real-world evidence and clinical operations
  • Contribute to scientific publications and external conference presentations
  • Mentor newer Analysts and junior team members, providing technical and professional guidance
  • Track task statuses against specified timelines
  • Assure data quality, integrity, and confidentiality of information
  • Review professional journals and publications to help solve complex research questions and keep informed of current trends

What You Bring to TriNetX:
  • Bachelor's degree in a health-related field or an equivalent combination of education and experience
  • 5+ years of experience in healthcare, clinical research, clinical trial design or execution, feasibility, or patient recruitment, preferably in a pharma/CRO setting
  • Demonstrated experience working with patient data including clinical information systems, EMR, claims, etc.
  • Familiarity with clinical data coding systems and/or computer-based clinical search tools and data analytics
  • Strong research skills and the ability to locate and synthesize clinical information
  • Proven ability to manage complex client relationships and translate business needs into data-driven solutions
  • Strong written, verbal, and presentation communication skills; experience presenting to external clients
  • Organized, detail-oriented, and able to manage workload to meet deadlines
  • Self-starter capable of working independently and collaboratively within a diverse team

Preferred
  • Advanced degree (MPH, MS, or equivalent)
  • Familiarity/proficiency with the TriNetX LIVE™ platform

Learn more about TriNetX:
To learn more about us, please check out our website, blog, and Careers page - and be sure to follow us on LinkedIn.
Interested in joining our community?
TriNetX is an Equal Opportunity Employer. All persons are considered for employment without regard to their race, color, creed, religion, national origin, ancestry, citizenship status, age, disability or handicap, sex or gender, marital status, sexual orientation, genetic information, gender identity, veteran status, or any other characteristic or status protected by applicable federal, state or local laws.
This Organization Participates in E-Verify
This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9.
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For more information on E-Verify, or if you believe that your employer has violated its E-Verify responsibilities, please contact DHS.
888-897-7781 https://www.e-verify.gov/

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