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Clinical Research Scientist Jobs (NOW HIRING)

ICON

Director, Clinical Research Scientist

Raleigh, NC · On-site +1

Director, Clinical Research Scientist 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 ...

Irhythmtech

Sr Clinical Scientist

The Senior Clinical Research Scientist is responsible for the leading scientific aspects of clinical research for assigned project(s) and will work closely with Clinical Research Operations ...

iRhythm Holdings, Inc.

Sr Clinical Scientist

The Senior Clinical Research Scientist is responsible for the leading scientific aspects of clinical research for assigned project(s) and will work closely with Clinical Research Operations ...

Plexus Worldwide

Research Scientist

Scottsdale, AZ · On-site

Research Scientist - Gut Health & Clinical Research The Role The Research Scientist is responsible for building the scientific foundation that differentiates our gut health portfolio through ...

Plexus Worldwide

Research Scientist

Scottsdale, AZ · On-site

Research Scientist - Gut Health & Clinical Research The Role The Research Scientist is responsible for building the scientific foundation that differentiates our gut health portfolio through ...

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How much do clinical research scientist jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for clinical research scientist in the United States is $56.32, according to ZipRecruiter salary data. Most workers in this role earn between $43.99 and $67.31 per hour, depending on experience, location, and employer.

What is a clinical research scientist?

Clinical research scientists are professionals who design, conduct, and analyze clinical trials to evaluate the safety and effectiveness of new drugs, medical devices, or treatment protocols. They work closely with healthcare professionals, regulatory agencies, and research organizations to ensure that studies comply with ethical standards and regulatory requirements. Their work is crucial in bringing new medical advancements to market and improving patient care.

What does a clinical research scientist do?

A clinical research scientist conducts research, usually in the medical or health care field. As a clinical research scientist, your job duties may include analyzing samples or researching a disease, often through clinical trials. You then summarize your findings in a report. You may work in a lab, hospital, or a research university. If you work in a university, your job duties include applying for research grants, but you may have an administrative assistant to which you can delegate this work. Especially in academia, your end goal is to publish this work for the scientific community.

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

To thrive as a Clinical Research Scientist, you need a strong background in life sciences, clinical trial design, and data analysis, typically supported by an advanced degree such as a PhD or PharmD. Familiarity with regulatory guidelines (e.g., GCP, FDA), statistical software (like SAS or R), and electronic data capture systems is essential. Attention to detail, problem-solving abilities, and effective communication skills are important for managing complex studies and collaborating with multidisciplinary teams. These skills and qualities ensure accurate research outcomes, regulatory compliance, and successful advancement of clinical projects.

What are some common challenges faced by clinical research scientists during clinical trials?

Clinical Research Scientists often encounter challenges such as ensuring participant recruitment meets study timelines, maintaining strict adherence to regulatory and ethical guidelines, and effectively managing large volumes of data. Collaboration with cross-functional teams—including physicians, regulatory affairs, and data management—is essential for resolving issues and ensuring trial integrity. Staying adaptable and communicative helps overcome obstacles and ensures the trial progresses smoothly.

What is the difference between Clinical Research Scientist vs Clinical Research Associate?

AspectClinical Research ScientistClinical Research Associate
Required CredentialsBachelor's or higher in life sciences, often with advanced degrees; certifications like CCR or RAC beneficialBachelor's degree in life sciences or related field; certifications like CCRA or RAC often preferred
Work EnvironmentResearch labs, pharmaceutical companies, or academic institutions; involved in designing and analyzing studiesMonitoring sites, ensuring protocol compliance, and managing trial logistics
Employer & Industry UsagePharmaceutical, biotech, and academic research organizationsClinical trial sites, CROs, pharmaceutical companies

While both roles are essential in clinical research, Clinical Research Scientists focus on study design, data analysis, and scientific development, whereas Clinical Research Associates primarily oversee trial conduct at sites, ensuring compliance and data integrity.

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Clinical Research Scientist jobs near you
Infographic showing various Clinical Research Scientist 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 $117,151 per year, or $56.3 per hour.

Director, Clinical Research Scientist

Icon plc

Raleigh, NC

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 5 days ago

Job description

Director, Clinical Research Scientist

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.


What You Will Do:

  • Development of protocols for clinical studies.

  • Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans.

  • Drafting of clinical scientific documents such as IND, IND amendments, Clinical Study Reports, Investigator Brochures, Annual Reports, and other health authorities submissions.

  • Responsible for providing clinical input into eCRF design, SAP, and TLFs.

  • Monitor, review, and summarize clinical safety and efficacy data in ongoing studies.

  • Collaborate with study team members to conduct timely and thorough review of study data using best practices and available tools to identify and evaluate data trends.

  • Will lead the clinical matrix teams for assigned studies, represent clinical development on project teams and serve as liaison to project teams, CRO's and others.

  • Provide clinical updates on assigned studies to Sr. management, Project Teams, Joint Project Teams and/or Steering Committees (if appropriate), Clinical sub-teams, internal strategy, and governance meetings, eDMC meetings, steering committees, advocacy groups, scientific advisory boards, and publications committees.

  • Liaise with cross functions on training of current studies, results, meeting with lead PIs/KOLs at conferences; present as needed.

  • Develop relationships with appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design.

  • Contribute to writing and review of study abstracts, posters, oral presentations, and manuscripts for assigned studies.

Your Profile:

  • Degree in scientific/life-sciences field. Pharm.D. or Ph.D. preferred.

  • Minimum of 4 - 6 years of experience in research with at least 3 or more years of clinical research/drug development experience are required for Director level.

  • Experience in Immunology field is required.

  • Ability to multi-task and work in a fast-paced environment.

  • Excellent written and oral communication skills.

  • Strong Analytical ability.

  • Ability to accommodate up to 20% travel or as business dictates.


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 requesthere.

Are you a current ICON Employee? Please click here to apply

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