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Clinical Science Jobs in Dallas, TX (NOW HIRING)

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 ...

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Clinical Science information

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$27.1K

$119.7K

$233.4K

How much do clinical science jobs pay per year?

As of Sep 6, 2026, the average yearly pay for clinical science in Dallas, TX is $119,742.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,515.00 and $179,101.00 per year, depending on experience, location, and employer.

What is clinical science?

Clinical science is a field of study that focuses on research and practices related to human health and disease, particularly as they apply to patient care. It involves the investigation of the causes, development, diagnosis, and treatment of illnesses through laboratory research, clinical trials, and patient-focused studies. Professionals in clinical science often work in hospitals, research institutions, or pharmaceutical companies, contributing to advances in medical knowledge and healthcare. The field bridges the gap between laboratory research and clinical practice, ensuring that scientific discoveries lead to improved patient outcomes.

What are some common challenges faced by professionals in clinical science roles, and how can they be addressed?

Professionals in Clinical Science often encounter challenges such as managing complex clinical trial protocols, ensuring regulatory compliance, and coordinating effectively with cross-functional teams. Navigating changing study requirements and tight timelines can also be demanding. To address these challenges, it's important to stay organized, maintain up-to-date knowledge of regulatory guidelines, and foster strong communication with colleagues in clinical operations, data management, and regulatory affairs. Leveraging project management tools and proactively seeking clarification on study objectives can also help Clinical Scientists succeed in their roles.

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

To thrive as a Clinical Scientist, you need a solid grounding in biological or biomedical sciences, often supported by an advanced degree such as an MSc or PhD, along with relevant clinical laboratory experience. Familiarity with laboratory information management systems (LIMS), specialized diagnostic equipment, and certifications like HCPC registration (in the UK) are typically required. Analytical thinking, attention to detail, and effective communication are crucial soft skills for interpreting results and collaborating with healthcare teams. These competencies ensure accurate diagnostics, patient safety, and the advancement of medical research and treatments.

What is the difference between Clinical Science vs Clinical Research Coordinator?

AspectClinical ScienceClinical Research Coordinator
Required CredentialsBachelor's or higher in life sciences, certifications like CCRP or CCRA often preferredBachelor's degree in health sciences or related field, often with certification like CCRP
Work EnvironmentPharmaceutical companies, biotech firms, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry and academia for drug development and clinical trialsPrimarily in clinical trial sites managing patient data and study logistics

Clinical Science professionals focus on designing, analyzing, and overseeing clinical trials, often working in labs or industry settings. Clinical Research Coordinators manage day-to-day trial operations at research sites, ensuring protocol adherence and patient safety. Both roles require similar credentials but differ in responsibilities and work environments.

Is clinical science a promising career?

Clinical science is a growing field that involves conducting research to improve patient care and develop new treatments. It often requires strong analytical skills, knowledge of biology and medicine, and relevant certifications or advanced degrees. The demand for clinical scientists is expected to increase with advancements in healthcare and medical research.

What can you do as a clinical scientist?

A clinical scientist conducts research and analyzes data to improve patient care, often working in laboratories or clinical settings. They may develop new diagnostic tools, oversee clinical trials, and collaborate with healthcare professionals, requiring strong analytical skills and knowledge of medical sciences.

What do you do in clinical science?

A clinical scientist conducts research and analysis to improve patient care, often working in laboratories or healthcare settings. They may develop and evaluate medical tests, work with clinical data, and collaborate with healthcare professionals to translate research into practice, often requiring knowledge of biology, medicine, and relevant regulations.

What are the most commonly searched types of Clinical Science jobs in Dallas, TX?

The most popular types of Clinical Science jobs in Dallas, TX are:

What cities near Dallas, TX are hiring for Clinical Science jobs?

Cities near Dallas, TX with the most Clinical Science job openings:

Infographic showing various Clinical Science job openings in Dallas, TX as of August 2026, with employment types broken down into 3% As Needed, 76% Full Time, 14% Part Time, and 7% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $119,742 per year, or $57.6 per hour.

Senior Clinical Scientist

Icon plc

Dallas, TX

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago


Key responsibilities

  • Design and conduct clinical studies to evaluate the safety and efficacy of treatments.

  • Author, review, and approve clinical protocols, analysis plans, study reports, and regulatory submissions.

  • Collaborate with cross-functional teams to develop protocols, summarize analysis, and support clinical program strategies.


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 requesthere.

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