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Clinical Scientist Ii Jobs (NOW HIRING)

Clinical Scientist II

Carlsbad, CA ยท On-site

$125K - $140K/yr

... by supporting clinical research and scientific evidence generation efforts. Working cross ... At least 2 years of medical device experience required (spine industry a plus). * Knowledge ...

Clinical Scientist II

Carlsbad, CA ยท On-site

$125K - $140K/yr

... by supporting clinical research and scientific evidence generation efforts. Working cross ... At least 2 years of medical device experience required (spine industry a plus). * Knowledge ...

... by supporting clinical research and scientific evidence generation efforts. Working cross ... At least 2 years of medical device experience required (spine industry a plus). * Knowledge ...

Contribute to the advancement of ATEC's spine surgery technologies by supporting clinical research and scientific evidence generation efforts. Working cross-functionally, this role will lead study ...

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Clinical Scientist II - Clinical Laboratory Scientist Location: Santa Rosa, California Job ID: ABOJP00047267 Division: Toxicology Diagnostics Assignment Dates: August 31, 2026-December 31, 2026 Work ...

Clinical Scientist II - C

Santa Rosa, CA ยท On-site

$50 - $54/hr

Clinical Scientist II - C Location: Santa Rosa, California Duration: 4 Months 100% Onsite Responsibilities: * Adequately display the knowledge and ability to carry out approved tests to comply with ...

Clinical Scientist II - C

Santa Rosa, CA ยท On-site

$47 - $52/hr

Must be licensed by the state of California under BPC, Chapter 3 as a Clinical Laboratory Scientist ... Nice to Have: * Minimum 2+ years' experience in a toxicology laboratory working with mass ...

Clinical Scientist II - C

Santa Rosa, CA ยท On-site

$47.85 - $52.85/hr

Must be licensed by the state of California under BPC, Chapter 3 as a Clinical Laboratory Scientist ... Nice to Have: Minimum 2+ years' experience in a toxicology laboratory working with mass ...

Applies clinical science principles and knowledge to guide cross-functional partners and ... 2 years of writing CIPs, CSRs in medical device industry. โ€ข Writes literature reviews and ...

Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP ... The Clinical Scientist is a key member of the team and partners closely with other clinical team ...

Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP ... The Clinical Scientist is a key member of the team and partners closely with other clinical team ...

Applies clinical science principles and knowledge to guide cross-functional partners and ... of 2 years of writing CIPs, CSRs in medical device industry. Writes literature reviews and ...

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Clinical Scientist Ii information

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$28

$54

$81

How much do clinical scientist ii jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical scientist ii 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 is a Clinical Scientist II?

A Clinical Scientist II is a mid-level professional who designs, conducts, and oversees clinical research studies, often in the pharmaceutical, biotechnology, or healthcare industries. They are responsible for ensuring studies comply with regulatory standards, analyzing clinical data, and contributing to the development of new medical treatments. Their role may include supervising junior staff, collaborating with other scientists and clinicians, and preparing technical reports or publications. Clinical Scientist II positions typically require a relevant advanced degree and a few years of experience in clinical research.

What are the typical daily responsibilities of a Clinical Scientist II, and how do they interact with cross-functional teams?

As a Clinical Scientist II, your daily responsibilities often include designing and overseeing clinical trial protocols, analyzing data, and ensuring compliance with regulatory standards. You will regularly collaborate with cross-functional teams such as clinical operations, biostatistics, regulatory affairs, and medical writing to ensure the smooth execution of trials. Effective communication and project management skills are essential, as you may also participate in meetings with external partners and provide scientific input on study progress. This role offers the opportunity to contribute directly to advancing clinical research while working in a dynamic, team-oriented environment.

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

A Clinical Scientist II typically requires advanced knowledge in biomedical sciences, clinical trial design, and data analysis, often supported by a relevant master's or PhD degree. Familiarity with statistical software, electronic data capture systems, and regulatory compliance tools (such as GCP certification) is essential. Strong analytical thinking, attention to detail, and effective communication skills help distinguish top performers in this role. These competencies ensure precise study execution, accurate data interpretation, and effective collaboration with cross-functional teams in clinical research.

What is the difference between Clinical Scientist Ii vs Clinical Scientist I?

AspectClinical Scientist IiClinical Scientist I
Required CredentialsBachelor's or Master's degree in life sciences, relevant certificationsBachelor's degree, entry-level position, fewer certifications
Work EnvironmentResearch labs, clinical trial sites, pharmaceutical companiesSimilar settings, often supervised by more experienced scientists
Employer & Industry UsagePharmaceutical, biotech, healthcare organizationsSame industries, typically an entry-level role
Common Search & ComparisonYesYes

The Clinical Scientist II typically has more experience, advanced certifications, and greater responsibilities than the Clinical Scientist I. Both roles work in similar environments within the pharmaceutical and healthcare industries, but the Clinical Scientist II is often involved in more complex projects and decision-making processes.

More about Clinical Scientist Ii jobs
Infographic showing various Clinical Scientist Ii job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,877 per year, or $54.7 per hour.

Clinical Scientist II

Alphatec Spine

Carlsbad, CA โ€ข On-site

$125K - $140K/yr

Full-time

Re-posted 17 days ago


Job description

Contribute to the advancement of ATEC’s spine surgery technologies by supporting clinical research and scientific evidence generation efforts. Working cross-functionally, this role will lead study design and protocol execution, management and analysis of datasets, and translation of findings into clear technical documentation and scientific communications that demonstrate product value and clinical impact.

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Partner cross-functionally with Marketing, Regulatory, R&D to identify evidence gaps and align research studies with product and business objectives.
  • Build relationships with key opinion leaders (KOLs) to generate clinician collaboration and relevant research projects, building and growing customer and investigator relationships that drive credibility in our products and organization.
  • Lead the design of clinical research protocols evaluating ATEC’s implant, biologics and surgical procedure portfolio, incorporating rigorous statistical methodology, including endpoint selection, power calculations, and statistical analysis plans.
  • Organize and manage large datasets data from research studies, ensuring accuracy, traceability, and proper documentation.
  • Compile, critically analyze, and interpret research data across multiple data modalities.
  • Prepare clear, complete and accurate technical engineering documentation.
  • Contribute to the dissemination of scientific findings through presentation and writing for both internal and external audiences, including interim reports, conference abstracts, presentations, manuscripts, product/procedural training and collateral; assist investigators or customers in the preparation and delivery of research results.
  • Collaborate closely with other members of the Scientific Affairs team, through meetings and interactions to gather technical and clinical support as well as to ensure alignment of the research activities within the team.
  • Work on problems of moderate scope where analysis of situations or data requires a review of a variety of factors.
  • Exercise judgment within defined procedures and practices to determine appropriate action.
  • Normally receives general instructions on routine work, detailed instructions on new projects or assignments.

Requirements

The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Minimum of Bachelors' degree in a field of science or engineering required, MS or PhD preferred. At least 2 years of medical device experience required (spine industry a plus).
  • Knowledge, understanding, and application of the conduct of clinical investigations involving humans in accordance ICH/GCP, US Code of Federal Regulations (CFR), and the ethical principles that guide clinical research consistent with the principles of the Nuremberg Code, the Belmont Report and the Declaration of Helsinki;
  • Proficiency in conducting literature searches and critically evaluating and communicating findings.
  • Strong understanding of clinical research and statistical/analytical methods.
  • Strong technical writing skills with ability to communicate results to internal and external customers.
  • Knowledge of orthopedics research, particularly spine, is a plus;
  • Familiarity with electronic data capture systems (EDC, EMR), data analysis, and data visualization.
  • Experience in technical writing, peer-reviewed literature retrieval and publishing.
  • Detail-oriented, resourceful problem solver, with effective organizational skills.
  • Ability to work in a fast-paced environment.

Equal Employment Opportunity & Other Disclosures

ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws.

For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable).

At this time, ATEC Spine does not sponsor employment visas for this position. Candidates must be authorized to work in the United States without the need for current or future employer sponsorship.

Salary Range

Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $125,000 to $140,000 Full-Time Annual Salary