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Clinical Science Jobs (NOW HIRING)

Director, Clinical Science

Hampton, NJ · On-site

$81K - $110K/yr

The Director, Clinical Science is a strategic scientific leader responsible for clinical study design, clinical data review, and execution of clinical development programs supporting innovative ...

Director, Clinical Science

Boston, MA · On-site

$86K - $118K/yr

As the Director, Clinical Science, you will lead the clinical science function responsible for developing the evidence that supports WHOOP's regulated and unregulated health features, with a ...

$59K - $80K/yr

Reporting to the Senior Director, Clinical Science, the Director of Clinical Science provides scientific and clinical leadership for Phase 1-3 clinical trials, including first-in-human studies ...

Director, Clinical Science

Boston, MA · On-site

$86K - $118K/yr

As the Director, Clinical Science, you will lead the clinical science function responsible for developing the evidence that supports WHOOP's regulated and unregulated health features, with a ...

Director, Clinical Science

San Francisco, CA · On-site

$220K - $250K/yr

About the Role >>> Director, Clinical Science As the Director, Clinical Science reporting to the Vice President, Clinical Science, you will play a key role in one of our ongoing clinical studies. You ...

Director, Clinical Science

Boston, MA · On-site

$220K - $250K/yr

About the Role >>> Director, Clinical Science As the Director, Clinical Science reporting to the Vice President, Clinical Science, you will play a key role in one of our ongoing clinical studies. You ...

Director, Clinical Science

San Diego, CA · On-site +1

$236K - $255K/yr

An integral member of the Janux Therapeutics' Clinical Development team; the Director, Clinical Science will support the strategic planning and execution of clinical-stage programs for one of the the ...

$59K - $80K/yr

Overview The Senior Director, Clinical Science is a strategic scientific leader responsible for shaping clinical development strategy, overseeing clinical study design, and directing the ...

Director, Clinical Science

San Diego, CA · On-site

$236K - $255K/yr

An integral member of the Janux Therapeutics' Clinical Development team; the Director, Clinical Science will support the strategic planning and execution of clinical-stage programs for one of the the ...

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Clinical Science information

See salary details

$27.5K

$121.3K

$236.5K

How much do clinical science jobs pay per year?

As of Sep 14, 2026, the average yearly pay for clinical science in the United States is $121,346.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $181,500.00 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.
More about Clinical Science jobs

What cities are hiring for Clinical Science jobs?

Cities with the most Clinical Science job openings:

What are the most commonly searched types of Clinical Science jobs?

The most popular types of Clinical Science jobs are:

What states have the most Clinical Science jobs?

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

Infographic showing various Clinical Science job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $121,346 per year, or $58.3 per hour.

Director, Clinical Science

San Carlos, CA • On-site

Scorpion Therapeutics
51 - 200 employees

$96K - $131K/yr

Other

Posted 15 days ago


Job description

Overview / Role

Director, Clinical Science develops Clinical Development Plans (CDPs) and supports assigned Medical Directors/Clinical Science Physicians and the Head of Clinical Science with deliverables for assigned assets/indications.

Responsibilities
  • - Participate in Clinical Development Core Team (CSCT) and Clinical Sub-Team (CST) meetings; interface with Biomarkers, Biometrics, Business Development, Clinical Operations, Legal, Logistics/Manufacturing Ops, PK/PD, Process Development, Project Management, Quality Assurance, Regulatory Affairs, Translational Medicine, and other groups.
  • - Represent Clinical Science in operational meetings (e.g., SMT).
  • - Support training for new CSCT members.
  • - Maintain up-to-date therapeutic/disease area scientific and clinical knowledge; collaborate with internal/external stakeholders (investigators, clinicians, scientists, KOLs).
  • - Support clinical science inputs to CS strategy and Lifecycle Plans (LCPs); contribute to CTP development; gather/analyze data to create the CS plan.
  • - Provide clinical science support for studies/programs: literature searches; input on study designs; design protocols/manuals/forms.
  • - Collaborate on consistent ICF, eligibility, dose modification, safety, CRFs, and CRF instructions; coordinate document completion.
  • - Write/review clinical science documents (protocol summaries, safety monitoring plans, investigator brochures, etc.); support safety narrative reviews.
  • - Develop/provide input for presentations and study communications; support site training.
  • - Review and discuss clinical reporting documents; track and support protocol/ICF amendments.
  • - Support internal/external meetings and communications strategies; coordinate scientific meeting submissions; write/review abstracts/posters/content.
  • - Support completion/submission of regulatory filings and required clinical documentation; lead/complete special projects as assigned.
Qualifications / Skills
  • - 7+ years oncology clinical trial experience; 5+ years clinical science/clinical development.
  • - Data listing review experience (mandatory).
  • - Advanced degree preferred (PhD/PharmD/MD).
  • - Cell therapy clinical development experience preferred.
  • - Experience authoring experimental protocols and/or study results/conclusions.
  • - In-depth Phase 1–4 drug development knowledge.
  • - Strong analytical skills; data analysis/interpretation and clinical relevance experience.
  • - Comprehensive product/safety profile knowledge; GCP/ICH and regulatory guideline knowledge (FDA/EMEA/NICE).
  • - Strong Microsoft Office skills (Word, PowerPoint, Excel).
  • - Excellent project management; communication and influencing skills; strong written/presentation skills.
  • - Ability to travel (~25%).
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