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Clinical Science Consultant Jobs (NOW HIRING)

The Clinical Science Consultant is responsible for leading non-branded, evidence-based education for Primary Care Providers (PCPs) to improve early identification and diagnosis of cardiac arrhythmias ...

The Clinical Science Consultant is responsible for leading non-branded, evidence-based education for Primary Care Providers (PCPs) to improve early identification and diagnosis of cardiac arrhythmias ...

VP, Clinical Science

OR · On-site +1

... formal consultation process. The position is required to ensure that the quality and the ... Scientific background with university degree and MD required * 10+ years Clinical experience with ...

Clinical Scientist - Oncology

Boston, MA · On-site

$116K - $182K/yr

Represent Clinical Science on regional and global clinical development teams * Contribute to the ... Experience within pharmaceutical, CRO, healthcare consulting, biomedical research or clinical ...

Clinical Business Consultant - Digital Biomarkers NNIT is one of the world's leading consultancies ... The role combines client delivery, scientific excellence, clinical integration, and business ...

Senior Medical Consultant The Senior Medical Consultant (SMC) will work as a strategic partner with ... operations, clinical science, medical monitoring, and regulatory affairs consistent with ...

Data Science Analyst II

Austin, TX · On-site

$72 - $88/hr

Serves as a data science consultant to clinical and operational leaders. * Translates ambiguous questions into structured analytical methods. * Leads meetings to gather requirements and present ...

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Clinical Science Consultant information

See salary details

$25.5K

$118.4K

$229K

How much do clinical science consultant jobs pay per year?

As of Aug 27, 2026, the average yearly pay for clinical science consultant in the United States is $118,374.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,000.00 and $155,500.00 per year, depending on experience, location, and employer.

What is a clinical science consultant?

A Clinical Science Consultant is a professional who provides scientific and clinical expertise to healthcare organizations, pharmaceutical companies, or research teams. They help interpret clinical data, support the development and implementation of clinical trials, and offer insights on regulatory compliance and best practices. Their work ensures that medical products or studies meet scientific standards and are conducted safely and ethically. Clinical Science Consultants often act as a bridge between scientific research and clinical practice, helping to translate findings into real-world applications.

How does a clinical science consultant typically collaborate with cross-functional teams in a healthcare setting?

Clinical Science Consultants frequently work alongside medical affairs, regulatory, and commercial teams to ensure scientific accuracy and compliance in clinical projects. They often serve as a bridge between research, development, and field teams, providing expert guidance and insights to support product development, clinical trials, and educational initiatives. Effective communication and teamwork are essential, as the role involves translating complex clinical data for diverse audiences and facilitating smooth project execution across departments.

What are the key skills and qualifications needed to thrive as a clinical science consultant, and why are they important?

To thrive as a Clinical Science Consultant, you need a strong background in life sciences or pharmacy, analytical expertise, and experience in clinical research or medical affairs, typically supported by an advanced degree such as PharmD, PhD, or MD. Familiarity with clinical trial protocols, regulatory guidelines, and data analysis software like SAS or Medidata is often required. Exceptional communication, problem-solving, and relationship-building skills enable effective collaboration with healthcare professionals and stakeholders. These skills are crucial for ensuring accurate scientific exchange, supporting evidence-based decisions, and driving successful clinical outcomes.

What is the difference between Clinical Science Consultant vs Medical Science Liaison?

AspectClinical Science ConsultantMedical Science Liaison
Required CredentialsTypically advanced degrees (PhD, PharmD, MD)Typically advanced degrees (PhD, PharmD, MD)
Work EnvironmentResearch settings, pharmaceutical companies, clinical trial supportMedical affairs, pharmaceutical companies, healthcare providers
Employer & Industry UsagePharmaceutical, biotech, medical device industriesPharmaceutical, biotech industries
Common Search & ComparisonYesYes

The Clinical Science Consultant and Medical Science Liaison roles share similar credentials and industry settings. While both engage with healthcare professionals and support clinical or scientific information, Clinical Science Consultants often focus on research and clinical trial support, whereas Medical Science Liaisons primarily facilitate medical information dissemination and scientific exchange. Understanding these differences helps professionals choose the right career path or job opportunity.

More about Clinical Science Consultant jobs

What states have the most Clinical Science Consultant jobs?

States with the most job openings for Clinical Science Consultant jobs include:

Infographic showing various Clinical Science Consultant job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $118,374 per year, or $56.9 per hour.

Full-time

Re-posted 5 days ago


Job description

Career-defining. Life-changing.

At iRhythm, you'll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every day, we collaborate, create, and constantly reimagine what's possible. We think big and move fast, driven by our commitment to put patients first and improve lives. We need builders like you. Curious and innovative problem solvers looking for the chance to meaningfully shape the future of cardiac health, our company, and your career

About This Role:

The Clinical Science Consultant is responsible for leading non-branded, evidence-based education for Primary Care Providers (PCPs) to improve early identification and diagnosis of cardiac arrhythmias in the outpatient setting. This role focuses on advancing disease state awareness, reducing diagnostic gaps driven by comorbidity overlap, and supporting appropriate use of ambulatory cardiac monitoring (ACM) within the standard of care.

Through strategic provider engagement and deployment of risk-based clinical tools, this role will help shift diagnosis upstream, reduce acute care utilization, and strengthen overall healthcare system integrity by enabling more efficient, cost-effective, and timely patient care.

Key Responsibilities

Clinical Education & Provider Engagement

  • Develop and deliver compliant, non-promotional educational programs on cardiac arrhythmias tailored to PCP audiences.
  • Translate current and emerging scientific literature into actionable insights relevant to primary care practice.
  • Establish credibility as a clinical resource and thought partner to PCPs and care teams.

Disease State Awareness & Diagnostic Gap Closure

  • Educate providers on the link between common comorbidities and increased arrhythmia risk.
  • Address symptom overlap and the risk of diagnostic overshadowing in primary care populations.
  • Communicate the downstream impact of delayed diagnosis, including increased HCRU, hospitalizations, readmissions, and cost of care.

Outpatient Diagnostic Optimization

  • Promote the role of PCPs in initiating appropriate diagnostic pathways, including ACM use within guidelines.
  • Highlight system barriers (e.g., cardiology access delays) and opportunities for earlier diagnosis in primary care.
  • Align education to PCP performance metrics, quality measures, and population health initiatives.

Ambulatory Monitoring Education (Holter vs. LTCM)

  • Educate PCPs on the clinical considerations, appropriate use cases, and limitations of short-duration monitoring (24-48 hour Holter) compared to longer-term continuous monitoring (LTCM) within current standards of care.
  • Highlight the relationship between symptom frequency, arrhythmia burden, and diagnostic yield when selecting monitoring duration.
  • Provide evidence-based context on how monitoring duration may impact diagnostic accuracy, time to diagnosis, and downstream care decisions.
  • Educate providers on emerging evidence demonstrating that reliance on short-duration monitoring-particularly when guided by perceived frequent symptoms-may result in missed diagnostic opportunities due to the intermittent and unpredictable nature of many arrhythmias.
  • Support PCP understanding of when extended monitoring may be appropriate for patients with intermittent, infrequent, or unexplained symptoms.

Clinical Tool Implementation

  • Support adoption of a symptom- and risk-based questionnaire to identify high-risk patients appropriate for ACM.
  • Guide integration of risk stratification tools into clinical workflows to improve diagnostic accuracy and efficiency.

Healthcare System Integrity & Value Optimization

  • Educate providers on how delayed or missed arrhythmia diagnoses contribute to system inefficiencies, including avoidable emergency department visits, inpatient admissions, and fragmented care pathways.
  • Position early, outpatient diagnosis as a mechanism to reduce unnecessary utilization and preserve healthcare resources.
  • Reinforce the role of PCP-driven diagnostic pathways in supporting care continuity, reducing variability, and improving system-level performance.
  • Align educational messaging to value-based care principles, emphasizing cost containment, quality improvement, and optimized resource allocation.

Cross-Functional Collaboration

  • Partner with Medical Affairs, Clinical Research, Market Access, and Commercial teams to ensure aligned, evidence-based messaging.
  • Provide field insights to inform publications, ongoing research, and educational strategy.
  • Contribute to development of scalable education models and best practices.

Performance Expectations & Incentive Alignment

  • Performance objectives and incentives are aligned to measurable impact on PCP engagement and adoption of appropriate, guideline-consistent diagnostic pathways within assigned markets.
  • Emphasis is placed on increasing PCP participation in arrhythmia identification and management in geographies with established specialty utilization, supporting a more integrated and efficient care delivery model.
  • Success is measured by the ability to drive upstream diagnostic behavior change, expand disease state awareness, and improve alignment between primary and specialty care.

Education & Experience

  • Minimum of 8 years of related experience with a Bachelor's degree; or 6 years and a Master's degree; or a PhD with 3 years experience; or equivalent experience.
  • Active Registered Nurse (RN) license, MSN, DNP, or equivalent clinical experience preferred
  • 7+ years clinical experience (cardiology, electrophysiology, or primary care strongly preferred)
  • 3+ years in clinical education, provider engagement, or medical affairs
  • Experience educating PCPs or working within primary care settings preferred


Location:

Remote - US

Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.

Estimated Pay Range

$115,000.00 - $149,000.00

As a part of our core values, we ensure an inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws.

iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at taops@irhythmtech.com

About iRhythm Technologies
iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm's vision is to deliver better data, better insights, and better health for all.

Make iRhythm your path forward. Zio, the heart monitor that changed the game.

There have been instances where individuals not associated with iRhythm have impersonated iRhythm employees pretending to be involved in the iRhythm recruiting process, or created postings for positions that do not exist. Please note that all open positions will always be shown here on the iRhythm Careers page, and all communications regarding the application, interview and hiring process will come from a @irhythmtech.com email address. Please check any communications to be sure they come directly from @irhythmtech.com email address. If you believe you have been the victim of an imposter or want to confirm that the person you are communicating with is legitimate, please contact taops@irhythmtech.com. Written offers of employment will be extended in a formal offer letter from an @irhythmtech.com email address ONLY.

For more information, see https://www.ftc.gov/business-guidance/blog/2023/01/taking-ploy-out-employment-scams and https://www.ic3.gov/Media/Y2020/PSA200121