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Clinical Science Jobs (NOW HIRING)

Director, Clinical Science

Boston, MA ยท 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

Boston, MA ยท On-site

$130 - $180/hr

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

OR ยท On-site +1

$79K - $108K/yr

We are seeking a Director, Clinical Science to architect trial strategies and protocol execution for our oncology molecular diagnostics portfolio, with a dedicated focus on signal Studies and ...

Director, Clinical Science

Boston, MA ยท 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

New York, NY ยท On-site

$212K - $261K/yr

As a Director within Clinical Science, you'll play a critical role in ensuring study protocols are executed appropriately and that the study data is both appropriate and pristine. On a daily basis ...

Director, Clinical Science

New York, NY ยท Remote

$212K - $261K/yr

We are seeking a Director-level Clinical Scientist who can oversee all clinical aspects of a clinical trial(s). This would include: planning and authoring clinical deliverables (protocols, amendments ...

Director, Clinical Science

$81K - $111K/yr

We are seeking a Director, Clinical Science to architect trial strategies and protocol execution for our oncology molecular diagnostics portfolio, with a dedicated focus on signal Studies and ...

Director, Clinical Science

San Francisco, CA ยท 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

Basking Ridge, NJ ยท On-site

$202 - $303/hr

Represents Clinical Science in Project Team, possibly as the Clinical Science Lead; act as the subject matter expert to provide scientific direction to Clinical Operations and other functions.

Director, Clinical Science

Boston, MA ยท On-site

$86K - $118K/yr

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

The Clinical Science Consultant is responsible for leading non-branded, evidence-based education for Primary Care Providers (PCPs) to improve early identification and diagnosis of cardiac arrhythmias ...

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Showing results 1-20

Clinical Science information

See salary details

$27.5K

$121.3K

$236.5K

How much do clinical science jobs pay per year?

As of Aug 20, 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 August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $121,346 per year, or $58.3 per hour.

Director, Clinical Science

Celldex Therapeutics

Hampton, NJ โ€ข On-site

Other

Medical, Retirement, PTO

Posted 14 days ago


Job description

Overview
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 therapies. This individual will play a central role in translating scientific and medical insights into robust clinical studies and development strategies, while leading the interpretation of clinical data to inform key program decisions.
Working closely with Clinical Science physicians, Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, Medical Writing, Biomarker/Translational Research, Pharmacovigilance, and Medical Affairs, the Director, Clinical Science will provide leadership across all phases of development, with particular emphasis on protocol development and study design, data review and interpretation, and data-driven decision making.
Responsibilities
Clinical Study Design and Development Strategy
  • Lead the design and development of clinical study protocols, protocol amendments, and associated study documents across all phases of development.
  • Partner with Clinical Science physicians and cross functional stakeholders to define study objectives, endpoints, eligibility criteria, study procedures and visit schedule, safety monitoring plans, and statistical considerations.
  • Ensure study designs are scientifically rigorous, operationally feasible, and aligned with regulatory and development objectives.
  • Contribute to clinical development plans, indication expansion strategies, and overall asset development decisions.
  • Integrate translational, biomarker, pharmacokinetic/pharmacodynamic (PK/PD), and patient-centered endpoints into clinical development programs.
  • Evaluate emerging scientific, competitive, clinical, and regulatory information to inform development strategies.

Clinical Data Review and Interpretation
  • Lead ongoing review and interpretation of clinical trial data, including efficacy, safety, biomarker, PK/PD, immunogenicity, and patient-reported outcomes.
  • Develop and implement data review strategies in collaboration with Biostatistics and Data Management.
  • Identify emerging trends, clinical signals, and development risks and provide recommendations to study teams and senior leadership.
  • Lead clinical review meetings and contribute to study conclusions, integrated analyses, and clinical development recommendations.
  • Present clinical data and program updates to governance committees, senior management, and cross-functional teams.
  • Support benefit-risk assessments and key development decisions throughout the product lifecycle.

Clinical Trial Execution and Scientific Oversight
  • Serve as the Clinical Science lead for assigned studies and development programs.
  • Provide scientific oversight during study conduct to ensure high-quality execution and data integrity.
  • Collaborate with Clinical Operations to support study startup, enrollment, protocol adherence, and issue resolution.
  • Participate in investigator meetings, advisory boards, and interactions with key opinion leaders and external experts.
  • Contribute to inspection readiness and compliance with GCP, ICH guidelines, and applicable regulatory requirements.

Regulatory and Scientific Contributions
  • Author and review clinical sections of regulatory documents, including INDs, CTAs, Investigator Brochures, Clinical Study Reports, briefing packages, periodic safety reports, annual reports, and marketing applications.
  • Support interactions with global health authorities and responses to regulatory inquiries.
  • Collaborate with Regulatory Affairs and Medical Writing to ensure high-quality and compliant clinical documentation.
  • Contribute to scientific publications, abstracts, posters, presentations, and congress materials.

Cross-Functional Leadership
  • Partner closely with Clinical Science physicians, Data management, Biomarker/Translational Research, Clinical Operations, Biostatistics, Safety, Regulatory Affairs, Medical Writing, and Medical Affairs.
  • Represent Clinical Science on cross-functional project teams, governance committees, and portfolio discussions.
  • Drive alignment across functions to support efficient decision-making and program execution.
  • Mentor and develop Clinical Scientists and contribute to building a culture of scientific excellence and continuous improvement.

Qualifications
  • Advanced degree in a scientific, healthcare, or related discipline preferred (e.g., PhD, PharmD, MD, DO, MS, MPH, NP, PA, or equivalent).
  • 10+ years of clinical research, clinical development, or clinical science experience within the biotechnology, pharmaceutical, or CRO industry.
  • Demonstrated experience leading clinical study design, protocol development, and clinical data review activities.
  • Experience serving as Clinical Science Lead for Phase 1 through Phase 3 clinical trials.
  • Proven track record of interpreting complex clinical datasets and translating findings into development strategy.
  • Experience supporting regulatory submissions and health authority interactions.
  • Experience in Immunology, autoimmune diseases, inflammatory disorders, or related therapeutic areas strongly preferred.
  • Biotechnology industry experience preferred.
  • Deep understanding of clinical trial methodology, study design, endpoint development, and statistical concepts.
  • Expertise in clinical data review and interpretation of efficacy, safety, biomarker, PK/PD, and translational data.
  • Strong knowledge of GCP, ICH guidelines, and global regulatory requirements.
  • Excellent scientific writing, communication, and presentation skills.
  • Strategic thinker with strong scientific judgment and analytical skills.
  • Proven ability to influence cross-functional teams and senior stakeholders.
  • Strong leadership, collaboration, and decision-making capabilities.
  • Ability to thrive in a fast-paced, innovative biotechnology environment.

Compensation Statement
The expected base salary for this position is: $176659.00 to $229427.00. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Subject to eligibility and applicable plan terms, compensation includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page
Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.