Senior Clinical Study Analyst

TriNetX, LLC; Cambridge (MA); Hybrid; USD 120,000 - 170,000; Full time

Job summary

TriNetX, LLC, located in Cambridge, MA, seeks a Sr. Clinical Study Analyst to support clinical research and trial design. The role combines data analysis, cohort identification using TriNetXLIVE, and consultative guidance to pharma and CRO clients.

The position involves travel, mentoring, and contribution to publications, with opportunities to advance platform adoption and real-world evidence capabilities. Strong communication and coding skills are essential.

Qualifications

• Bachelor's degree in health-related field or equivalent
• 5+ years in healthcare, clinical research, or related areas
• Experience with patient data and clinical information systems
• Familiarity with coding systems (ICD, CPT, SNOMED) and data analytics
• Strong written, verbal, and presentation skills

Responsibilities

• Translate eligibility criteria and query for patient cohorts using TriNetXLIVE
• Apply clinical coding schemes to define cohorts
• Understand trial eligibility criteria and map to data sources
• Lead live demos and training with minimal oversight
• Serve as primary contact for pharma, CROs, and healthcare clients
• Handle high volume of platform and analytics questions
• Manage multiple customer engagements with prioritization
• Collaborate with Clinical Feasibility & Analytics and other teams
• Document feedback on usability and potential features
• Support sales and training for platform users
• Mentor junior analysts and track progress
• Review literature to stay informed on trends

Skills

Healthcare experience

Clinical research

Data analytics

EMR data

Coding systems

Communication

Client relations

Project management

Independent work

Education

Bachelor's degree in health-related field

Advanced degree (MPH/MS)

Tools

TriNetXLIVE

EMR systems

Job description

100 Cambridgepark Dr, Cambridge, MA 02140, USA

Job Description

Posted Thursday, July 30, 2026 at 10:00 AM

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 extensiveexpertiseacross 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 creatingself-sufficient users of our platform and driving product adoption in the process. The ideal candidate is someone willing tolearnour platform, data, and tools whileutilizingexisting clinical information and skills to discovernew approachesin solving challenging matters.

What You Will Be Doing:

• Independently translate eligibility criteria and query for patient cohorts usingTriNetXLIVE™
• 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 ofTriNetXLIVE™ with minimal oversight
• Serve as primary contact for pharma, biotech, CRO, and healthcare organization clients toidentify, analyze and interpret data relevant to clinical questions and needs, and provide consultativeassistancevia written, oral, or in-person presentation methods
• Handle a high volume and complexity of daily questions from pharma and healthcare organization usersregardingplatform 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 ofTriNetXon 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 buildexpertisein 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 toTriNetX:

• Bachelor's degree in a health-related field or an equivalent combination of education and experience
• 5+ yearsof 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 tolocateand 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/proficiencywiththeTriNetXLIVE™ platform

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.

E-Verify Works for Everyone

For more information on E-Verify, or if you believe that your employer has violated its E-Verify responsibilities, please contact DHS.

100 Cambridgepark Dr, Cambridge, MA 02140, USA