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Clinical Scientist Jobs (NOW HIRING)

As a Clinical Scientist I, you will support the development, design, and execution of Neuralink's clinical evidence strategy. This role focuses on translating product and research objectives into ...

Clinical Scientist

Palo Alto, CA ยท On-site +1

$134K - $155K/yr

Clinical Scientist Location:Palo Alto, CA As a Clinical Scientist, you will support the Clinical Affairs team in executing clinical programs aligned with Hyperfine's strategic priorities. You will ...

The successful candidate will bring strong clinical science expertise and experience supporting studies with sites across both the United States and Asia-Pacific (APAC) regions. As part of a lean and ...

Clinical Scientist

Princeton, NJ ยท On-site

$80K - $120K/yr

We are seeking a motivated Clinical Scientist to join our clinical development team and contribute to the advancement of innovative therapeutic programs. This role provides an excellent opportunity ...

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Clinical Scientist information

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How much do clinical scientist jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical scientist in the United States is $54.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $68.27 per hour, depending on experience, location, and employer.

What are some common challenges clinical scientists face when collaborating with multidisciplinary teams?

Clinical Scientists often work alongside physicians, nurses, laboratory technologists, and data analysts, which can present challenges in communication and aligning goals. Differences in terminology and priorities between clinical and research staff may require extra effort to ensure everyone is on the same page. Regular meetings, clear documentation, and a willingness to learn from other disciplines are essential for effective collaboration. Addressing these challenges proactively helps ensure that clinical trials and research projects run smoothly.

What is the difference between Clinical Scientist vs Clinical Research Associate?

AspectClinical ScientistClinical Research Associate
Required CredentialsTypically requires a degree in life sciences, advanced degrees preferred, certifications like CCRP or RACRequires a degree in health sciences or related field, often with certifications like CRA or RAC
Work EnvironmentResearch institutions, pharmaceutical companies, biotech firms, laboratoriesClinical trial sites, hospitals, research organizations
Employer & Industry UsagePharmaceutical, biotech, medical device industriesContract research organizations, pharmaceutical companies, hospitals

Clinical Scientists focus on designing, analyzing, and interpreting clinical research studies, often working in labs or research settings. Clinical Research Associates primarily oversee the progress of clinical trials at sites, ensuring compliance and data accuracy. Both roles are essential in clinical research but differ in responsibilities and work environments.

What is a clinical scientist?

A clinical scientist is an expert in the life sciences that studies blood, tissue, cells, and other parts of a living organism to advance medical research and knowledge about living things. While your duties can vary significantly, most clinical scientists collaborate with a larger research team to create and run experiments and publish the results. There is a vast range of specialized fields to pursue. For example, you might focus on the study of biomedicine, specifically medications and treatments used to fight illness and disease. Positions are available at hospitals, clinics, universities, laboratories, and a variety of other research facilities.

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 strong background in biomedical science, laboratory techniques, and data analysis, usually supported by a relevant degree and professional registration. Familiarity with laboratory information management systems (LIMS), diagnostic equipment, and compliance with regulations like ISO 15189 is essential. Attention to detail, problem-solving, and effective communication are crucial soft skills for collaborating with healthcare teams and interpreting results. These skills ensure accurate diagnostics, patient safety, and high standards of clinical research and laboratory operations.

What qualifications does a clinical scientist need?

A clinical scientist typically needs a relevant undergraduate degree in a scientific or healthcare field, followed by postgraduate training or a master's degree in clinical science or a related discipline. Professional registration or accreditation, such as with a health or scientific regulatory body, and strong analytical and technical skills are also important for working in clinical laboratories or research settings.
What cities are hiring for Clinical Scientist jobs? Cities with the most Clinical Scientist job openings:
What are the most commonly searched types of Clinical Scientist jobs? The most popular types of Clinical Scientist jobs are:
Who are the top companies hiring for Clinical Scientist jobs? The top employers for Clinical Scientist jobs are:
What states have the most Clinical Scientist jobs? States with the most job openings for Clinical Scientist jobs include:
Infographic showing various Clinical Scientist job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $113,877 per year, or $54.7 per hour.

Clinical Scientist

Neuralink

Austin, TX โ€ข On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 9 days ago


Job description

About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what's possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink's BCI technology for use in people!
Job Description and Responsibilities:
As a Clinical Scientist I, you will support the development, design, and execution of Neuralink's clinical evidence strategy. This role focuses on translating product and research objectives into clinical study designs, supporting data analysis, and ensuring scientific rigor across clinical programs.
This individual is a self-driven and analytically strong individual who can contribute to clinical strategy while executing with precision. The ideal contributor is detail-oriented, collaborative, and comfortable working in a fast-paced, multidisciplinary environment.
In this role, you will:
  • Support the design and development of clinical study protocols, including endpoints, inclusion/exclusion criteria, and statistical considerations
  • Contribute to clinical strategy by translating research and product goals into evidence-generating study plans
  • Partner with other team members to support execution of clinical studies and ensure alignment between scientific intent and operational delivery
  • Build and maintain strong working relationships with internal teams, investigators, and external partners
  • Support preparation of study-related documents, including protocols, investigator brochures, clinical study reports, and regulatory submissions
  • Contribute to EDC and CRF design by ensuring alignment between protocol objectives, endpoints, and data collection strategy
  • Translate clinical and scientific requirements into structured, high-quality data capture and validation approaches
  • Assist in data review, analysis, and interpretation to evaluate safety and performance outcomes
  • Contribute to development of abstracts, presentations, and publications
  • Support interactions with ethics committees (e.g., IRB, RECs) and regulatory bodies as needed
  • Ensure scientific and clinical activities are conducted in compliance with Good Clinical Practice (GCP), applicable regulations, and internal SOPs
  • Identify data trends, inconsistencies, or risks and proactively communicate findings to the broader team

Required Qualifications:
  • Familiarity with statistical methods or programming (e.g., Python, R)
  • 5+ years of experience in clinical research or scientific roles within medical devices or related fields
  • Strong analytical and problem-solving skills with the ability to interpret complex data
  • Familiarity with clinical study design, endpoints, and data analysis concepts
  • Working knowledge of Good Clinical Practice (GCP) and basic regulatory requirements (e.g., ISO 14155)
  • Ability to work cross-functionally with clinicians, engineers, and operational teams
  • Strong written and verbal communication skills, particularly in scientific and technical contexts
  • High attention to detail and ability to manage multiple priorities

Preferred Qualifications:
  • Experience with neurological, neurosurgical, or implantable medical device studies
  • Experience supporting protocol development, data analysis, or clinical reporting
  • Publications or scientific presentations in biomedical engineering or neuroscience
  • PhD in neuroscience, biomedical engineering, or a related field

Additional Requirements and Competencies:
  • Willingness to travel (up to ~20-30%) to support site visits, investigator meetings, and study activities
  • Strong organizational and documentation skills
  • Ability to work independently while collaborating closely with cross-functional teams
  • Adaptability and comfort in a fast-paced, high-growth environment
  • Commitment to scientific rigor, patient safety, and high-quality evidence generation

Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees' success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$108,000-$200,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
  • An opportunity to change the world and work with some of the smartest and most talented experts from different fields
  • Growth potential; we rapidly advance team members who have an outsized impact
  • Excellent medical, dental, and vision insurance through a PPO plan
  • Paid holidays
  • Commuter benefits
  • Meals provided
  • Equity (RSUs) *Temporary Employees & Interns excluded
  • 401(k) plan *Interns initially excluded until they work 1,000 hours
  • Parental leave *Temporary Employees & Interns excluded
  • Flexible time off *Temporary Employees & Interns excluded