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Clinical Science Consultant Jobs (NOW HIRING)

Johnson and Johnson

Head of Clinical Science

Provides technical consultations to other departments for registration purposes, acquisitions, Marketing, Legal and Sales Training. * Responsible for annual budgets for Clinical Science (Santa Ana ...

IQVIA

Director, Clinical Science, Cronos

Bethlehem, PA

$79K - $107K/yr

Ensure Clinical Team escalations are managed appropriately and in consultation with other ... Clinical Science, as required. * Perform data preparation activities-including cleaning ...

IQVIA

Director, Clinical Science, Cronos

Bethlehem, PA · On-site

$79K - $107K/yr

Ensure Clinical Team escalations are managed appropriately and in consultation with other ... Clinical Science, as required. * Perform data preparation activities-including cleaning ...

Telix Pharmaceuticals (AMER)

OR · On-site

... formal consultation process. The position is required to ensure that the quality and the ... Scientific background with university degree and MD required * 10+ years Clinical experience with ...

Amgen

OR · On-site

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Provide guidance and oversight in the identification and management of collaborators, consultants ...

Bioclinica

Clinical Scientist

OR · On-site +1

Build and maintain professional relationships with external consultants, key opinion leaders, and ... Whether you're advancing clinical science, building innovative technology, or supporting our global ...

Clario Tech

Clinical Scientist

Build and maintain professional relationships with external consultants, key opinion leaders, and ... Whether you're advancing clinical science, building innovative technology, or supporting our global ...

Outpace Bio

Clinical Scientist

Seattle, WA · On-site

... rigorous science. Our Commitment to Diversity At Outpace Bio, we believe that the highest ... members, consultants, asset team leaders, and clinical trial site staff. * Serve as technical ...

Actalent

Director, Clinical Scientist

Wilmington, DE

Develop and maintain productive relationships with external consultants and key experts to support ... We help visionary companies advance their engineering and science initiatives through access to ...

Integrated Resources INC

Clinical Scientist

Edison, NJ · On-site

Initiates, directs and executes all pre-clinical scientific research and/or development strategies ... Interfaces with various departments and serves as internal consultant. Additional Information All ...

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All JobsClinical Science Consultant Jobs

Clinical Science Consultant information

See salary details

$25.5K

$118.4K

$229K

How much do clinical science consultant jobs pay per year?

As of Jun 12, 2026, the average yearly pay for clinical science consultant in the United States is $118,374.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,000.00 and $155,500.00 per year, depending on experience, location, and employer.

How much does a science consultant make?

A Clinical Science Consultant typically earns between $70,000 and $120,000 annually, depending on experience, location, and the complexity of the role. Salaries may also include bonuses and benefits, and the position often requires strong scientific knowledge and communication skills.

What is a Clinical Science Consultant?

A Clinical Science Consultant is a professional who provides scientific and clinical expertise to healthcare organizations, pharmaceutical companies, or research teams. They help interpret clinical data, support the development and implementation of clinical trials, and offer insights on regulatory compliance and best practices. Their work ensures that medical products or studies meet scientific standards and are conducted safely and ethically. Clinical Science Consultants often act as a bridge between scientific research and clinical practice, helping to translate findings into real-world applications.

What do consultant clinical scientists do?

Consultant clinical scientists are healthcare professionals who apply scientific knowledge to develop, evaluate, and improve medical tests, devices, and treatments. They often work in laboratories or clinical settings, analyzing data, ensuring compliance with regulations, and supporting the implementation of new technologies. Strong analytical skills, relevant certifications, and knowledge of laboratory procedures are essential in this role.

What does a clinical consultant do?

A clinical science consultant provides expert advice on medical and scientific information related to healthcare products, therapies, or devices. They often collaborate with healthcare professionals, support clinical trials, and ensure compliance with regulatory standards, using their knowledge of science and medicine to inform product development and education.

How does a Clinical Science Consultant typically collaborate with cross-functional teams in a healthcare setting?

Clinical Science Consultants frequently work alongside medical affairs, regulatory, and commercial teams to ensure scientific accuracy and compliance in clinical projects. They often serve as a bridge between research, development, and field teams, providing expert guidance and insights to support product development, clinical trials, and educational initiatives. Effective communication and teamwork are essential, as the role involves translating complex clinical data for diverse audiences and facilitating smooth project execution across departments.

How much do clinical scientist consultants make in the US?

Clinical Science Consultants in the US typically earn between $80,000 and $120,000 annually, depending on experience, location, and certifications. Salaries can vary based on the complexity of projects and the level of expertise required in clinical research and scientific communication.

What are the key skills and qualifications needed to thrive as a Clinical Science Consultant, and why are they important?

To thrive as a Clinical Science Consultant, you need a strong background in life sciences or pharmacy, analytical expertise, and experience in clinical research or medical affairs, typically supported by an advanced degree such as PharmD, PhD, or MD. Familiarity with clinical trial protocols, regulatory guidelines, and data analysis software like SAS or Medidata is often required. Exceptional communication, problem-solving, and relationship-building skills enable effective collaboration with healthcare professionals and stakeholders. These skills are crucial for ensuring accurate scientific exchange, supporting evidence-based decisions, and driving successful clinical outcomes.

What is the difference between Clinical Science Consultant vs Medical Science Liaison?

AspectClinical Science ConsultantMedical Science Liaison
Required CredentialsTypically advanced degrees (PhD, PharmD, MD)Typically advanced degrees (PhD, PharmD, MD)
Work EnvironmentResearch settings, pharmaceutical companies, clinical trial supportMedical affairs, pharmaceutical companies, healthcare providers
Employer & Industry UsagePharmaceutical, biotech, medical device industriesPharmaceutical, biotech industries
Common Search & ComparisonYesYes

The Clinical Science Consultant and Medical Science Liaison roles share similar credentials and industry settings. While both engage with healthcare professionals and support clinical or scientific information, Clinical Science Consultants often focus on research and clinical trial support, whereas Medical Science Liaisons primarily facilitate medical information dissemination and scientific exchange. Understanding these differences helps professionals choose the right career path or job opportunity.

More about Clinical Science Consultant jobs
What states have the most Clinical Science Consultant jobs? States with the most job openings for Clinical Science Consultant jobs include:
What job categories do people searching Clinical Science Consultant jobs look for? The top searched job categories for Clinical Science Consultant jobs are:
What are popular job titles related to Clinical Science Consultant jobs? For Clinical Science Consultant jobs, the most frequently searched job titles are:
Clinical Science Consultant jobs near you
Infographic showing various Clinical Science Consultant job openings in the United States as of June 2026, with employment types broken down into 75% Full Time, 15% Part Time, and 10% Contract. Highlights an 85% In-person, 5% Hybrid, and 10% Remote job distribution, with an average salary of $118,374 per year, or $56.9 per hour.
Executive Director, Clinical Science

Executive Director, Clinical Science

Celldex Therapeutics

Hampton, NJ • On-site

$233K - $303K/yr

Other

Medical, Retirement, PTO

Posted 24 days ago

Job description

Overview
The Executive Director of Clinical Science is a key member of the Clinical Science Leadership Team and provides leadership, clinical strategy and direct oversight of clinical science deliverables, including overseeing the clinical scientists to ensure the design, data collection, and reporting of clinical studies is timely and consistent with high quality standards, applicable regulations and Celldex's overarching clinical development strategy.
Responsibilities
  • Lead, develop and manage a highly functional, productive, collaborative team of clinical scientists to ensure efficiency, quality, consistency and the achievement of timely deliverables across the programs, including but not limited to:
    • Create and train on standardized clinical science working processes
    • Establish cross-functional collaboration with colleagues in clinical development, clinical operations, medical affairs, regulatory affairs, commercial organizations as well as external physicians, expert consultants, and contracted vendors
    • Support medical directors in generation of strategic clinical development plans
    • Play a leadership role in the design of Phase 1-4 clinical studies
    • Own and manage the generation and drafting of key documents, including protocols, protocol amendments, IBs, CSRs, and clinical regulatory submissions
    • In collaboration with regulatory colleagues, compile submissions including clinical data summaries/analyses, such as briefing packages.
    • Leads clinical science contributions to BLA submission, including drafting content
    • Oversee the review, analysis, and reporting of clinical data in collaboration with medical directors to enable internal decision making and regulatory filings
    • Provide input into statistical analysis plans and data displays in accordance with regulatory and strategic objectives. Ensure data collection is consistent with/supportive of protocol and analysis plans.
    • Contribute to data cleaning efforts by performing clinical data reviews and providing training feedback to the Clinical Operations Team; provide guidance for issues that may impact clinical trials data generation, collection, and analysis
    • Participate in planning for interim data analyses and reviews, including Data Monitoring Committee (DMC) meetings
    • Own the development of Celldex scientific clinical presentations and publications (message development, message integration, content drafting, layout, internal and external review process, submission and speaker preparation), including but not limited to abstracts, presentations at medical/scientific meetings and manuscripts
    • Hire, onboard, train, manage, and develop clinical scientist team
      • Manage clinical scientist resourcing across programs
    • Assumes responsibility for individual deliverables as needed.

Qualifications
  • MS/MA degree or equivalent in a scientific or health care field required. PhD's preferred.
  • 10-15 years of experience in clinical research setting, including medical writing, protocol development, and oversight of (or close collaboration with) data management/analysis/reporting functions.
  • Extensive experience authoring clinical protocols, regulatory documents (IND sections, clinical study reports, investigator brochures), as well as scientific publication and presentations.
  • Experience with preparation of BLA
  • At least 4 years of experience in immunology & inflammation preferred
  • Demonstrated experience designing and executing clinical trials in all phases of clinical development, (Phase 1-3, post-marketing)
  • Proven ability to design and execute clinical development plans and interpret data for decision-making and external communication.
  • Strong knowledge of GCP and the end-to-end drug development process, including nonclinical, CMC, regulatory, pharmacovigilance, data management and clinical operations.
  • Experience recruiting, training, mentoring, managing and leading highly functional, productive teams.
  • Strategic thinker with an execution-focused mindset, well suited for a lean biotech environment.
  • Ability to work in an agile, fast paced environment.
  • Excellent written and verbal communication skills, with the ability to influence internal and external stakeholders.
  • Excellent project management skills.

Compensation
The expected base salary range for this position is $233,631 to $303,417.
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.
Compensation for this role 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.

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