clinical research analyst

Providence Swedish

<div>Description
We are seeking a highly organized and detail‑focused Regulatory Coordinator to support compliant and efficient research operations. In this role, you will contribute to the integrity of clinical research by ensuring documentation is accurate, timelines are met, and processes run smoothly. You will collaborate with research teams, support organizational standards, and help maintain a strong regulatory foundation that enables high‑quality research across the institution. This position is ideal for someone who excels in structured work, enjoys document coordination, and thrives in a research‑driven environment.
Key Responsibilities:
<ul><li>Prepares, facilitates, coordinates, and submits documentation required by federal, state and local regulations and institutional requirements relating to the conduct of research.</li>
<li>This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA‑required submissions which may include investigator 1572 forms, investigational new drug applications, device submissions such as Emergency use, HDE, Safety Reports, and other documents that may be required by a regulatory agency or the institution.</li>
<li>Leads the work of Research Assistants on a task-basis if applicable.</li>
<li>Provides on-the-job training, sets priorities and schedules workflow required to support project objectives.</li>
</ul>Providence Swedish caregivers are not simply valued &ndash; they&rsquo;re invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.
Required qualifications:
Bachelor's Degree Preferably in science, healthcare, or other related field -or<ul><li>-</li>
<li>Significant experience in research coordination or regulatory work may be substituted for educational requirements</li>
<li>2 years of experience in healthcare, research or clinical setting with regulatory compliance familiarity</li>
</ul>Why Join Providence Swedish?
Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our mission of improving the health and wellbeing of each patient we serve.
About Providence
At Providence, our strength lies in Our Promise of &ldquo;Know me, care for me, ease my way.&rdquo; Working at our family of organizations means that regardless of your role, we&rsquo;ll walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable.
Posted are the minimum and the maximum wage rates on the wage range for this position. The successful candidate's placement on the wage range for this position will be determined based upon relevant job experience and other applicable factors. These amounts are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits.
Applicants in the Unincorporated County of Los Angeles: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Unincorporated Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
About the Team
Providence Swedish is the largest not-for-profit health care system in the greater Puget Sound area. It is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. Whether through physician clinics, education, research and innovation or other outreach, we&rsquo;re dedicated to improving the wellbeing of rural and urban communities by expanding access to quality health care for all.
Providence is proud to be an Equal Opportunity Employer. We are committed to the principle that every workforce member has the right to work in surroundings that are free from all forms of unlawful discrimination and harassment on the basis of race, color, gender, disability, veteran, military status, religion, age, creed, national origin, sexual identity or expression, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law. We believe diversity makes us stronger, so we are dedicated to shaping an inclusive workforce, learning from each other, and creating equal opportunities for advancement.
For any concerns with this posting relating to the posting requirements in RCW 49.58.110(1), please click here where you can access an email link to submit your concern.
Requsition ID: 418083
Company: Swedish Jobs
Job Category: Research
Job Function: Clinical Support
Job Schedule: Full time
Job Shift: Day
Career Track: Clinical Professional
Department: 3909 SRE TUMOR INSTIT RESEARCH
Address: WA Seattle 1221 Madison
Work Location: Swedish First Hill 1221 Madison-Seattle
Workplace Type: Hybrid
Pay Range: $35.06 - $54.43
The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.</div>

Clinical Research Analyst - Tumor Institute

Elevate Clinical Research Solutions

Are you experienced in Medicare Coverage Analysis for clinical trials? Are you tired of unrealistic expectations, being treated like a number in a work queue, or feeling like your expertise isn&rsquo;t valued?At Elevate Clinical Research Solutions, we:<ul><li>Put people first. We prioritize strong working relationships and collaboration - with both our clients and each other.</li><li>Set realistic expectations. We deliver high-quality work with speed in a way that is sustainable, not causing burn out.</li><li>Rise together. We are all shareholders, so we truly share in our success as a team and all play an important role in continuously improving our services.</li></ul>What You&rsquo;ll DoAs a Senior Clinical Research Analyst, you will:<ul><li>Conduct Medicare Coverage Analyses (MCA) for clinical trials, ensuring compliance with CMS rules and billing requirements</li><li>Develop and support the creation, review, and negotiation of clinical trial budgets</li><li>Lead service delivery for a set of assigned client accounts, overseeing workflow and exceeding client expectations.</li><li>Mentor analysts and provide regular feedback on MCA work to continue to enhance the skills of the team</li></ul>What You&rsquo;ll NeedTo be successful in this role, you&rsquo;ll bring:<ul><li>Bachelor&rsquo;s degree in science, economics, or a related analytical field</li><li>Minimum of 3 years of recent experience in roles for which the primary focus or responsibility was completing MCAs for clinical trials</li><li>Experience completing MCAs on the most complex clinical trials, including multiple ARMs and complex therapeutic areas.</li><li>Experience working in an external, client-facing capacity</li><li>A track record of producing accurate, high-quality work and meeting deadlines</li><li>Strong written and verbal communication skills and comfort collaborating with multiple stakeholders</li><li>A proactive, solutions-oriented mindset</li></ul>What You&rsquo;ll Be a Part OfYou&rsquo;ll join a team that values both precision and people.This isn&rsquo;t an extreme-volume work queue environment where quality gets sacrificed for speed. Our analysts are trusted professionals who work collaboratively, support one another, and have the space to do work the right way.On our team, you can expect:<ul><li>A collaborative group of analysts - you won&rsquo;t be working in isolation</li><li>A team invested in continuous improvement, shared knowledge, and best practices</li><li>Leadership that prioritizes building trust, keeping an open door, and giving everyone a voice - balancing high expectations with flexibility and respect for life outside of work</li><li>Work that directly impacts research sites and makes trials more feasible and sustainable</li></ul>This position is intended to be a full time role, but may have some flexibility to start in a part time or limited capacity for the right candidate.Job Types: Full-time, Part-timePay: $90,000.00 - $105,000.00 per yearExperience:<ul><li>Medicare Coverage Analysis for clinical trials: 2 years (Preferred)</li></ul>Work Location: Remote

Senior Clinical Research Analyst - Medicare Coverage Analysis Expert

FlairsTech

<div><div><div><div>Requirements and responsibilities<div> 
Position Summary
The Clinical Research Data Analyst &ndash; Scientific Content &amp; Research is responsible for researching, curating, validating, and analyzing scientific and clinical data from reputable healthcare and life sciences sources. This role supports high-value client products by ensuring that scientific content, conference records, journal publications, and clinical trial data are accurate, structured, and publication-ready.
The ideal candidate is analytical, detail-oriented, and thrives in a fast-paced, collaborative environment. This role requires strong research capabilities, data interpretation skills, and the ability to transform complex scientific information into structured, reliable datasets.<div></div>
Key Responsibilities<ul><li>
Research and extract data from peer-reviewed journals, clinical trial registries, conference proceedings, and scientific databases.</li><li>
Collect, analyze, abstract, and structure scientific information into standardized formats.</li><li>
Maintain and update conference records (monthly) and journal records (annually), ensuring data accuracy and integrity.</li><li>
Perform quality assurance checks to validate data consistency and completeness.</li><li>
Conduct web-based research including scientific news sources, blogs, forums, and industry publications.</li><li>
Analyze published data related to clinical trials and life sciences research.</li><li>
Support data mapping, indexing, and source validation activities.</li><li>
Contribute to process improvement initiatives to enhance data curation workflows.</li><li>
Assist in identifying opportunities for automation to improve operational efficiency.</li><li>
Communicate progress, risks, and findings clearly to stakeholders.</li><li>
Maintain up-to-date documentation of procedures and workflows.</li></ul><div></div>
Required Skills &amp; Competencies<ul><li>
Strong understanding of clinical research and/or medical affairs.</li><li>
Knowledge of scientific publishing processes within biotech or pharmaceutical industries.</li><li>
Familiarity with conference schedules, abstract submissions, and publication timelines.</li><li>
Solid data mining, curation, and indexing experience using scientific databases.</li><li>
Strong analytical thinking and problem-solving capabilities.</li><li>
Advanced Microsoft Excel skills (data manipulation, formulas, structured datasets).</li><li>
Working knowledge of databases and query languages (e.g., SQL) is preferred.</li><li>
Comfortable working with large datasets.</li><li>
Strong written and verbal communication skills in English.</li><li>
Highly organized with strong attention to detail.</li><li>
Ability to work independently and collaboratively across teams and time zones.</li><li>
Technically adaptable and quick to learn new systems and tools.</li></ul><div></div>
Qualifications<ul><li>
Bachelor&rsquo;s degree in Pharmaceutical Sciences, Biomedical Sciences, Molecular Biology, Computer Science, or a related discipline.</li><li>
Experience working with scientific literature, clinical trial data, or healthcare databases.</li><li>
Proficiency in English (written and spoken).</li></ul><div></div>
Work Environment &amp; Expectations
This role requires high accuracy, accountability, and the ability to meet structured deadlines. Responsibilities may evolve over time in alignment with business needs, with appropriate training provided.</div></div></div></div></div>

Clinical Research Data Analyst

ZeOmega

<div>
 
 The Clinical Analyst is responsible for supporting the clinical research, development and design of clinical information systems and associated protocols for deployment to the ZeOmega product platforms. The Clinical Analyst participates as a member of the Clinical Content Team in representing the needs and requirements of the physician community and serves as an advocate in promoting the use of information technology in the clinical setting. The Clinical Analyst also works in partnership with ZeOmega leadership in system design, implementation and translation of clinician requirements into specifications for clinical protocols.
 
 
 
 
 
 
 PRINCIPLE JOB RESPONSIBILITIES:
 
 
 <ul>
 <li>
 Provides broad-based input into the design of the clinical information system protocols
 </li>
 <li>
 Facilitates clinician advisory groups in the design of clinical systems to support excellence in patient care plans
 </li>
 <li>
 Reviews medical informatics trends, experiences and approaches, develops technical and application implementation strategies and protocols
 </li>
 <li>
 Works in concert with Business Analysts (BA) and Subject Matter Experts (SME) to design and implement systems supporting care management and physician engagement regimens
 </li>
 <li>
 Facilitates design of clinical pathway models with physician, nursing and administrative leadership, and will assist in modification and annual review of these models to gain maximum efficacy
 </li>
 <li>
 Provides input into the development of clinical rules supporting identification, care management plans, potential gaps in care and protocol research as well as the design of clinical system features supporting protocol management and the use of the system to leverage the clinicians' time and maximize communication among stakeholders
 </li>
 <li>
 Participates in development and deployment of solutions that cluster information in disease and episodic categories for benchmarking, clinical severity, and variance analysis. Designs and evaluates collection of data for clinical purposes, including tracking and interpretation of outcomes
 </li>
 <li>
 Participates in determining content and design of care management and provider reports
 </li>
 <li>
 Ability to conduct worldwide medical/clinical literature, regulatory and program research to develop innovative health promotion and medical/behavioural health management programs
 </li>
 <li>
 Provide solution to Clinical problems identified across organization as Clinical SME
 </li>
 <li>
 Clinical experience of 5+ years in Hospital setup.
 </li>
 <li>
 Preferred experience in US healthcare market
 </li>
 <li>
 Preferred experience in medical informatics, Medical claims, Medical coding systems &amp; Health information systems (EMR/HER/HIS/LIS)
 </li>
 </ul>
 
 
 
 
 
 Education:
 
 Must be an MBBS
 
</div>

Clinical Analyst

Coforge

The Clinical Analyst will support provider outreach using healthcare workflows and provide clinical expertise. The position involves research, case resolution, reporting and cross functional collaboration to ensure accuracy and operational excellence. The role requires strong communication skills and analytical capabilities to manage client interactions through calls and email correspondence.
 Key Responsibilities
 <ul>
<li>Investigate and resolve provider inquiries, including dismissals (e.g., incorrect CPT codes, ineligible beneficiary) and no-response cases.</li>
<li>Conduct detailed case investigations and coordinate provider callbacks to share findings.</li>
<li>Develop, update, and standardize process documentation to support scalability.•Identify gaps, errors, and improvement opportunities across billing, coding, pends, denials, and utilization review.</li>
<li>Collaborate with operations, coding, QA, and client teams to ensure accurate and timely case resolution.</li>
<li>Analyze data trends and provide insights to support decision-making.</li>
<li>Handle inbound and outbound provider calls professionally to resolve concerns.</li>
<li>Respond to emails promptly with clear and accurate communication.</li>
<li>Participate in client/provider meetings, provider discussions, calibrations, andtroubleshooting sessions.</li>
<li>Prepare dashboards, audit summaries, SOP updates, and RCA documentation.</li>
<li>Ensure availability during business hours: 8:00 AM – 5 pm PM EST</li>
</ul>
Preferred Skills: 
<ul>
<li>Experience working with US payers or providers.</li>
<li>Working knowledge of ICD, CPT, and HCPC nomenclature.</li>
<li>Exposure to analytics platforms or BI tools.</li>
<li>Ability to work effectively in a fast-paced, SLA-driven environment.</li>
</ul>
Experience with Amazon Connect or similar call center software
 Required Skills Qualifications
 <ul>
<li>Preferred bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related healthcarediscipline.</li>
<li>Strong understanding of the US healthcare ecosystem.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Ability to manage calls and email interactions with internal and external stakeholders.</li>
<li>Proficiency in Excel, reporting tools, and structured documentation.</li>
</ul>
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LSU Health Sciences Center - New Orleans

<div>Title: IRB ANALYST 1, 2 or 3

Employee Type: Unclassified Staff

Department: VCAA-Institutional Review Board

Campus Location: VICE CHANCELLOR/ACADEMIC AFFAI

Job Summary/Basic Functions

The Institutional Review Board (IRB) is a federally mandated committee for institutions involved in research with human participants; it serves as a screening unit to review, evaluate, and make recommendations relative to research proposals that utilize human subjects. Under broad supervision and guidance from a faculty administrator, the IRB specialist is responsible for a complex range of activities for the Office of Research Services including, but not limited to: conducting pre-reviews of submissions to the IRB, including new protocols, continuing reviews, modifications, and unanticipated problems; attending IRB meetings and providing support to the IRB Chair and IRB Members, including writing and editing minutes of meetings; conducting quality control functions and post-approval monitoring; delivering relevant education programs; optimizing and streamlining departmental processes; and supervising and training IRB Coordinators and student helpers;. The incumbent also ensures compliance with federal regulations involving both Public Health Service and the Food &amp; Drug Administration.

Minimum Qualifications

Required Education: Bachelor's

Required Field of Study: Business, administration, healthcare, scientific field, public health, information technology or a directly related field from an accredited institution

Number of years required to perform the job: Analyst 1 - 2 years, Analyst 2 - 4 years, Analyst 3 - 6 years

Type of experience required to perform the job: Work experience in scientific or medical research, administrative support, healthcare, legal or regulatory compliance, or related areas. Analyst 2 &amp; 3 requires at least 2 &amp; 4 years of IRB experience respectively.

Substitution: Master's or Doctorate Degree will substitute for 2 years of non IRB-related professional experience or one year of IRB-related experience; or Bachelor's degree in a non-related field will be accepted with at least 4 years of direct experience in Human Subject research, IRB or medical research ethics 


Comprehensive benefits are available to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement plans; generous annual and sick leave; 14 paid holidays per year; and an employee health primary care clinic. See following link for more details on our benefits offerings: LSUHSC, New Orleans - Benefits

Other employee benefits include a full-service credit union, wellness benefits featuring complimentary fitness center membership for employees and their spouses, employee assistance program, campus assistance program, and pet insurance option. More information about these benefits can be found on this webpage: Additional Benefits</div>

IRB ANALYST 1, 2 or 3

Stryker

<div><h3 class="jobSectionHeader">Why join Stryker?</h3>
Looking for a place that values your unique talents? Discover Stryker's award-winning culture. 
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<h3 class="jobSectionHeader">
Job description</h3>
We are excited to be named one of the World&rsquo;s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.<div>
The Clinical Affairs Lead Analyst is responsible for supporting the clinical education and training associated primarily with the Transcatheter Arterialization of the Deep Vein (TADV) therapy, in addition to the broader peripheral vascular portfolio. This role focuses on teaching, guiding, and supporting sonographers, physicians, and clinical staff in mastering ultrasound surveillance techniques required for the safe and effective implementation and follow-up of this therapy. The successful candidate will possess deep clinical knowledge of TADV, its application in the CLTI patient population, and the ability to interpret TADV duplex studies. This role will collaborate closely with internal and external stakeholders to ensure clinical proficiency in all company supported venous and arterial diseases states, optimize imaging, and contribute to the ongoing evolution and standardization of all therapies.
The Clinical Affairs Lead Analyst plays a key role in Medical Education, supporting teams with high-quality, on-site and remote ultrasound training to ensure consistent, reliable imaging for total portfolio vascular care with an emphasis on TADV. Partnering closely with cross-functional groups and the commercial sales team, this position strengthens protocol adherence, enhances training impact, and helps maintain best-practice standards across all participating sites. This position is Remote with 75% travel requirements.
What you will do<ul><li>
Deliver clinical training programs for sonographers, physicians, and clinical staff related to ultrasound surveillance for TADV therapy and peripheral vascular disease states.</li><li>
Assist in the continuous improvement of ultrasound protocols and best practices.</li><li>
Provide onsite and remote clinical support and guidance to participating sites, ensuring the quality and consistency of ultrasound images for accurate diagnosis and treatment.</li><li>
Maintain thorough knowledge of clinical workflow, patient care considerations, and operational requirements</li><li>
Maintain accurate documentation of training, site support, and clinical observations.</li><li>
Participate in meetings, site visits, and other activities related to clinical education and therapy advancement.</li><li>
Assist in Vascular training content creation.</li><li>
Act as an internal ultrasound subject-matter expert and strategic resource across cross-functional teams, including Medical Affairs, Scientific Communications, Marketing, Health Economics, and R&amp;D, supporting aligned clinical, scientific, and commercial initiatives.</li><li>
Lead creation and review of training and education content, including clinical training programs - live and virtual, and educational assets for internal teams and external customers.</li><li>
Contribute to the development of consensus papers, peer-reviewed manuscripts, and scientific communications by providing technical expertise, clinical insights, and content review.</li><li>
Support scientific communication strategy by ensuring accuracy, clinical relevance, and consistency of ultrasound messaging across marketing, education, and publication efforts.</li><li>
Operate with a high degree of autonomy and self-direction to accomplish team objectives with minimal supervision.</li></ul>
What you need<ul><li><div>
Bachelor's degree or Associate's degree</div></li><li><div>
4+ years of experience in clinical ultrasound or medical imaging (if a bachelor's degree is acquired)</div></li><li><div>
8+ years of experience in clinical ultrasound or medical imaging (if an associate's degree is acquired)</div></li><li>
Strong clinical and technical knowledge of vascular sonography, including hemodynamics, ultrasound physics, deep venous and arterial duplex assessments, and physiologic studies required.</li><li>
Willingness to travel extensively (&gt;75%), including to clinical sites, meetings, and training.</li></ul> 
Preferred Qualifications<ul><li>
ARDMS RVT or CCI RVS credentials and certification are active.</li><li>
Direct vascular interventional experience in the OR, Cath Lab, IR suite, or Office Based Lab.</li><li>
Ability to build collaborative relationships across clinical, technical, and operational teams.</li></ul>
$110,100 - $183,400 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors. 
Posted Date: 02/23/2026 
This role will be posted for a minimum of 3 days.</div>
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&amp;D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.</div>

Clinical Affairs Lead Analyst

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10000 clinical research analyst jobs Near Me

Clinical Research Analyst - Tumor Institute

Senior Clinical Research Analyst - Medicare Coverage Analysis Expert

Clinical Research Data Analyst

Clinical Analyst

Clinical Analyst

IRB ANALYST 1, 2 or 3

Clinical Affairs Lead Analyst