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Clinical Science Jobs (NOW HIRING)

Janux Therapeutics

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 ...

BioNTech SE

Director, Clinical Science

Cambridge, MA · On-site

$168K - $268K/yr

As Director, Clinical Science (m/f/d), you will lead and shape clinical development strategies, playing a critical role in advancing our investigational drugs from concept to reality. You will ...

Merck & Co.

$86K - $118K/yr

The Senior Director, Clinical Science - Hematology is responsible for providing strategic Clinical Science leadership across the hematology disease area, with accountability spanning multiple studies ...

MSD

Senior Director of Clinical Science - Lung

Rahway, NJ · On-site

$81K - $110K/yr

The Senior Director, Clinical Science - Lung is responsible for providing strategic Clinical Science leadership across the lung disease area, with accountability spanning multiple studies, programs ...

Merck & Co.

$86K - $118K/yr

The Senior Director, Clinical Science - Lung is responsible for providing strategic Clinical Science leadership across the lung disease area, with accountability spanning multiple studies, programs ...

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Clinical Science information

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$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.
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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:

What job categories do people searching Clinical Science jobs look for?

The top searched job categories for Clinical Science jobs are:

Clinical Science jobs near you
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 Diego, CA • On-site

Janux Therapeutics
Biotechnology Research and Development • 11 - 50 employees
Learn more about Janux Therapeuticsexternal

$236K - $255K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 9 days ago

Job description

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 company’s early stage oncology platforms. This role partners closely with Clinical Operations to ensure effective trial conduct and supports the Clinical Lead in delivering critical trial milestones.

This role is perfect for individuals passionate about science-driven strategy and want to be at the forefront of immunotherapy innovation, as their opportunity to make a difference.

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
  • Support the design and implementation of development strategies for programs entering the clinic, providing strategic clinical science input for all assigned programs
  • Collaborate cross functionally with Clinical Operations team members to support the design and execution of clinical trials. This may include assistance in the development of essential clinical trial documents such as protocols, ICF documents/amendments, CRF’s, CSR’s, and Investigator Brochures
  • Aid in the development of the Data Review Plan and Data Review Strategy, ensuring that protocol-level deviations, eligibility criteria, study assessments & other aspects of the protocol are implemented consistently across the study
  • Perform clinical data review and identify clinical data insights through ongoing patient level review and trends analysis, working cross-functionally to monitor clinical data
  • Promote quality review of data with an emphasis on subject safety and eligibility, data integrity, trend identification, analysis and remediation, and identification of AEs/SAEs for medical review
  • Support ad-hoc Regulatory activities such as contributing by authoring/reviewing clinical portions of Regulatory Documents and/or posters, abstracts and manuscripts, and the preparation and conduct of meetings with regulatory agencies and/or external drug development consortiums
  • Develop and deliver upon clinical presentation slides and other materials for internal and external meetings
  • Maintain scientific and clinical knowledge in the specific therapeutic and disease areas of assignment
  • Other duties as required
EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES
  • BS in life sciences or related field; advanced degree (MS or PhD) in life sciences preferred
  • Minimum 8 years of industry experience, 5+ years of which dedicated to the conduct of clinical trials as a Clinical Scientist
  • Knowledge of oncology drug development and clinical trial processes, study design, statistics and clinical operations within a similar biotech and/or pharmaceutical environment
  • Skills to support program-specific data review and trend analysis
  • Knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees
  • Knowledge of GCP and regulatory requirements
  • Ability to critically evaluate data, literature and presentations
  • Ability to lead and work with cross-functional teams
  • Strong project management skills

$236,000 - $255,000 a year

In addition to a competitive base salary ranging from $236,000 to $255,000, we offer stock options, restricted stock units, a stock purchase plan (ESPP) and a target bonus. Janux also provides a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance.

Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and internal equity.

Job Type

Full-time

Benefits
  • Annual bonus program
  • Incentive stock option plan
  • 401k plan with flat non-elective employer contribution
  • Comprehensive medical insurance with 90-100% employer-paid premiums
  • Dental and vision insurance
  • HSA, FSA, and supplemental insurance plans (life, disability, accident, critical illness, hospital indemnity)
  • Unlimited PTO
  • Generous holiday schedule; includes summer and winter company shutdown
  • Relocation assistance
Schedule
  • Monday to Friday
Work authorization
  • United States (Required)
Additional Compensation
  • Annual targeted bonus %
Work Location
  • Hybrid preferred in San Diego office. Remote permitted upon approval, with ability to travel up to 25% for meetings or site visits as required.
EQUAL OPPORTUNITY EMPLOYER

Janux Therapeutics, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity.

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