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Senior Clinical Analyst Jobs in Raleigh, NC (NOW HIRING)

ICON

Senior Clinical Scientist

Raleigh, NC · On-site +1

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and ... Author/Review/Approve clinical protocols, analysis plans, study reports and regulatory submissions ...

Icon plc

Senior Clinical Scientist

Raleigh, NC · On-site

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and ... Author/Review/Approve clinical protocols, analysis plans, study reports and regulatory submissions ...

New

RSM

Supervisor - Epic Clinical Analyst

Raleigh, NC

Analyze current-state clinical workflows andidentifyopportunities to improve provider efficiency ... Supervise associates and senior associates by reviewing work quality, providing coaching, assigning ...

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Senior Clinical Analyst information

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How much do senior clinical analyst jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for senior clinical analyst in Raleigh, NC is $41.41, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $46.73 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a senior clinical analyst?

To thrive as a Senior Clinical Analyst, you need a deep understanding of clinical workflows, data analysis, and healthcare regulations, usually supported by a degree in health informatics, nursing, or a related field. Proficiency with tools such as electronic health records (EHRs), data analytics software (like SQL or SAS), and knowledge of clinical decision support systems is essential. Strong problem-solving abilities, communication skills, and attention to detail help build collaboration between clinical and IT teams. These skills and qualities are vital for optimizing clinical processes, ensuring regulatory compliance, and improving patient outcomes through data-driven insights.

How does a senior clinical analyst typically collaborate with cross-functional teams in a healthcare setting?

A Senior Clinical Analyst often works closely with physicians, nurses, IT professionals, and administrative staff to optimize clinical workflows and ensure effective use of healthcare data systems. This collaboration usually involves gathering requirements, translating clinical needs into technical specifications, and providing training or support for new system implementations. Regular meetings and project updates are common, and strong communication skills are essential for bridging the gap between clinical and technical teams. By fostering these cross-functional relationships, Senior Clinical Analysts help drive improvements in patient care and operational efficiency.

What is the difference between Senior Clinical Analyst vs Clinical Data Analyst?

AspectSenior Clinical AnalystClinical Data Analyst
Required CredentialsBachelor's degree in healthcare, life sciences, or related field; experience in clinical research; knowledge of EDC systemsBachelor's degree in health informatics, statistics, or related field; proficiency in data analysis tools
Work EnvironmentClinical research settings, pharmaceutical companies, healthcare organizationsData-focused roles in healthcare, research institutions, or biotech firms
Employer & Industry UsageUsed in clinical trials, healthcare analytics, pharmaceutical researchCommon in data management, healthcare analytics, research projects

The Senior Clinical Analyst typically has more experience and responsibilities related to overseeing clinical data processes and ensuring compliance, whereas the Clinical Data Analyst primarily focuses on analyzing and interpreting clinical data. Both roles require strong analytical skills and familiarity with healthcare data systems, but the Senior Clinical Analyst often plays a more strategic and supervisory role in clinical research projects.

How much do senior clinical analysts make in the US?

Senior clinical analysts in the US typically earn between $80,000 and $120,000 annually, depending on experience, location, and employer. They often require strong analytical skills, knowledge of healthcare data systems, and proficiency with tools like SQL and electronic health records.

What does a senior clinical analyst do?

A senior clinical analyst evaluates healthcare data and clinical systems to improve patient care and operational efficiency. They analyze electronic health records, develop reports, and collaborate with medical staff to optimize clinical workflows, often using tools like SQL, Excel, and clinical software. They typically require strong analytical skills, healthcare knowledge, and experience with data management tools.

What are popular job titles related to Senior Clinical Analyst jobs in Raleigh, NC?

For Senior Clinical Analyst jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Senior Clinical Analyst jobs in Raleigh, NC look for?

The top searched job categories for Senior Clinical Analyst jobs in Raleigh, NC are:

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Cities near Raleigh, NC with the most Senior Clinical Analyst job openings:

Senior Clinical Analyst jobs near you

Senior Clinical Scientist

ICON

Raleigh, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago

Job description

Senior Clinical Scientist (Hematology-Oncology)
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-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior Clinical Scientist at ICON, you will design and conduct clinical studies that evaluate the safety and efficacy of innovative treatments.
What You Will Do:
  • Provide strategic leadership and demonstrating accountability for the clinical programs supporting early clinical development and clinical pharmacology
  • Maintain updated knowledge of competitive landscape on current assets or evolving standards of care for indications of interest and provide subject matter expertise on cross-functional project teams
  • Author/Review/Approve clinical protocols, analysis plans, study reports and regulatory submissions in collaboration with physicians, statisticians and other critical functions.
  • Execute Clinical & Clinical Pharmacology studies in close collaboration with Clinical Operations
  • Review and summarize clinical safety or efficacy data in collaboration with the Medical Monitor
  • Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis
  • Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans
  • Draft and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports and other Health Authority submissions
  • Ensure adherence to agreed timelines and budgets to ensure prompt and accurate execution of deliverables from clinical studies and programs
  • Develop and maintain collaborative working relationships with appropriate consultants and external experts for subject matter expertise and protocol development
  • Compliant with departmental and broader organizational SOPs as fit for purpose, in compliance with current scientific standards and regulatory requirements
  • Participate in project teams and serve as liaison to project teams, CRO's, Clinical sub-teams, and others
  • Present data at scientific meetings, both internally and externally and author manuscripts in scientific journals

Your Profile:
  • At least 5 years' experience and a, PhD, PharmD or MD degree or at least 10 years' experience with BS/MS degree with emphasis on early development, clinical pharmacology or a related discipline
  • Ability to critically analyze problems and provide creative solutions
  • Excellent written and oral communication skills
  • Confidence and ability to present to and influence matrix teams and senior leaders
  • Ability to work independently, manage multiple priorities, and thrive in a dynamic environment
  • Genuine curiosity and drive to ask questions - looking for the 'why' of every project
  • Experience in clinical pharmacology, immunology or oncology is preferred
  • Early phase/Phase I experience required
  • Willingness to travel up to 20%, accommodations available for individuals with disabilities

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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