CrawlJobs Logo

Senior Clinical Scientist

blackrockneurotech.com Logo

Blackrock Neurotech

Location Icon

Location:
United States , Salt Lake City

Category Icon
Category:
Research and Development

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

Job Description:

The Senior Clinical Scientist role is suited to scientifically minded candidates with experience and interest in clinical research development and execution, supported by expertise in experimental design, data analysis, and scientific communication. Long-term success in this role will require contributions to high-impact research that advances the field of neurotechnology; developing research programs to support Blackrock Neurotech’s roadmap for brain-computer interfaces; and, building and maintaining strong collaborations with colleagues within Blackrock and in the academic community. This role will plan, execute, and supervise data acquisition and experimental protocols that fit within larger pre-clinical studies and clinical trials, including intraoperative electrophysiology studies and associated hardware testing, ensuring that study endpoints, workflows, and data quality expectations translate effectively across environments and strategically align with the company’s vision and goals.

Job Responsibility:

  • Lead and manage clinical research projects, collaborating with pre-clinical and multidisciplinary teams, and ensuring alignment with company goals and regulatory requirements
  • Partner between clinical and pre-clinical teams to develop and execute acute and intraoperative electrophysiology studies, including defining endpoints, coordinating execution workflows, and ensuring high-quality data acquisition
  • Support and/or coordinate hardware testing in the context of acute/intraoperative clinical studies (e.g., test planning, setup verification, troubleshooting, and structured capture of outcomes to inform development decisions)
  • Analyze and interpret complex data sets, providing actionable insights to guide BCI development
  • Collaborate with cross-functional teams, including engineering, regulatory, and clinical affairs, with emphasis on bridging clinical and pre-clinical stakeholders to align study execution and hardware testing needs
  • Prepare and present scientific reports, publications, and presentations to internal and external stakeholders
  • Stay current with advancements in neurotechnology and related fields to inform research strategies
  • Mentor and provide guidance to junior scientists and other team members

Requirements:

  • Ph.D. in Neuroscience, Biomedical Engineering, or a related field
  • Proven expertise in experimental design, data analysis, and scientific communication
  • Demonstrated experience working across pre-clinical and clinical research settings, with the ability to translate study objectives into executable protocols and comparable datasets across settings
  • Experience developing and/or executing acute and/or intraoperative electrophysiology studies
  • Strong analytical skills and proficiency with statistical software and data visualization tools, including analysis of electrophysiology and device performance data
  • Excellent written and verbal communication skills
  • Ability to work independently and as part of a collaborative team

Nice to have:

  • Experience with regulatory submissions and clinical trial design is a plus
  • Familiarity with neurotech and neuroscience research is highly desirable (including acute and intraoperative electrophysiology workflows and translation of methods between pre-clinical and clinical settings)
  • Experience in pre-clinical or clinical research, preferably in neuroscience-related fields
  • Comfort partnering with engineering teams to plan and document hardware testing performed during acute, intraoperative, and/or pre-clinical studies

Additional Information:

Job Posted:
January 19, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
Blackrock Neurotech - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Senior Clinical Scientist

Senior Clinical Data Scientist - Applied Data Enablement

Pivotal role focuses on enabling our customers to make informed decisions based ...
Location
Location
United States , Seattle
Salary
Salary:
155000.00 - 170000.00 USD / Year
truveta.com Logo
Truveta
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree or equivalent in a quantitative field such as computer science, engineering, statistics, mathematics, or economics
  • Minimum of 3 years of hands-on experience in data analytics, including proficiency in SQL, Spark, R, and/or Python, with a focus on executing data exploration, profiling, and validation projects
  • Proven track record of working effectively with cross-functional teams and communicating complex findings to diverse audiences
  • Ability to thrive in a fast-paced environment, demonstrating initiative and delivering high-quality results
  • Exceptional written and verbal communication skills, with the ability to convey project status, timelines, and project outcomes clearly
  • Proficient in applying generative AI and related tools across workstreams to enhance efficiency and scalability
Job Responsibility
Job Responsibility
  • Develop a deep understanding of Truveta Data, its characteristics, and its applications in clinical research
  • Create customer-facing reports and tutorials that summarize findings and provide actionable recommendations for research studies utilizing Truveta Data, driven by a prioritization list derived from customer and internal stakeholder needs
  • Design tailored artifacts and templates for multiple skill levels, serving as key inputs to enhance Truveta’s AI initiatives
  • Present findings in both written and oral formats to diverse audiences, including executive-level customers, detail-oriented analysts, and internal product and engineering teams
  • Engage with customers to understand research needs and effectively communicate results
  • Develop a deep understanding of Truveta Studio, our analytical platform
  • Write high-quality, reproducible analysis code in SQL, R, Python, and Spark, and share it with internal teams and customers for educational purposes
What we offer
What we offer
  • Comprehensive benefits with strong medical, dental and vision insurance plans
  • 401K plan
  • Professional development & training opportunities for continuous learning
  • Work/life autonomy via flexible work hours and flexible paid time off
  • Generous parental leave
  • Regular team activities (virtual and in-person)
  • Additional compensation such as incentive pay and stock options
  • Fulltime
Read More
Arrow Right

Oncology clinical scientist intern

The Global Oncology Internship Program at Johnson & Johnson is a comprehensive l...
Location
Location
Belgium , Beerse
Salary
Salary:
Not provided
https://www.randstad.com Logo
Randstad
Expiration Date
January 25, 2026
Flip Icon
Requirements
Requirements
  • Legally/permanently authorized to work in Belgium with no required sponsorships
  • Must be currently enrolled in an accredited University or College program throughout the duration of the internship
  • Must not be graduating before, during, or after the start or end of the internship program
  • Currently enrolled in biology, cell/molecular biology, chemistry, pre-med, nursing program, public health, biochemistry, biomedical engineering, oncology, clinical pharmacology, clinical or translational research, computational biology, precision medicine, or similar areas of study
  • Undergraduate students with completion of a minimum of four semesters at program start or graduate students are eligible
  • Minimum cumulative GPA of 3.0
  • Students in good standing, working towards the completion of an undergraduate or graduate degrees
  • Graduate students must be pursuing a master’s, PharmD, Physician Assistant or PhD or other clinical related degrees
  • Self-motivated, future scientist leaders passionate about drug development and clinical research
  • Detailed oriented with good organizational skills
Job Responsibility
Job Responsibility
  • Gaining overall understanding of clinical research and drug development including but not limited to Good Clinical Practices (GCPs), International Conference of Harmony (ICH) guidelines, and Standard Operating Procedures (SOPs)
  • Attend “Bench to Bedside” Lecture Series to gain knowledge of the drug development process and clinical research
  • Assisting with management of trial activities including patient tracking through screening process, and eligibility/enrollment reviews
  • Assisting with document processing and management within the electronic master file (i.e., vTMF)
  • Participating in department and team meetings
  • Participating in cross-functional team and clinical team meetings
  • Developing study training materials/documents
  • Shadowing key clinical and or functional roles for learning/development opportunities
  • Observing Site Initiation Visit (SIV) Meetings (if applicable for assigned projects)
  • Supporting Clinical Team with study start up activities during trial set up, and other study tasks during conduct, and close out (depending on the stage of the trial)
What we offer
What we offer
  • We offer an inclusive work culture that is open, innovative, and performance driven
  • Fulltime
!
Read More
Arrow Right

Senior Bioinformatics Scientist

We are looking for a Senior Bioinformatics Scientist to join a fast growing team...
Location
Location
United States , Menlo Park
Salary
Salary:
156060.00 - 176868.00 USD / Year
billiontoone.com Logo
BillionToOne
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD in Bioinformatics, Computational Biology, Computer Science, Bioengineering, Physics or related fields
  • 2+ years of experience developing robust and scalable bioinformatics pipelines
  • 2+ years of experience analyzing NGS data
  • Fluency in Python
  • Experience with Linux environment, GitHub and AWS
  • Excellent communication and presentation skills, ability to work across functional teams and with non-experts
Job Responsibility
Job Responsibility
  • Develop sophisticated and robust NGS analysis pipelines capable of processing tens of thousands of samples
  • Develop tests and test frameworks for NGS pipelines
  • Analyze and troubleshoot clinical NGS data
  • Analyze assay performance and contribute to publications that demonstrate the clinical validity and utility of our tests
  • Design new quality metrics and processes for clinical molecular diagnostic assays
  • Collaborate with R&D scientists to generate new scientific insights
  • Communicate assay performance and capabilities to clinical personnel at weekly meetings and to other non-clinical stakeholders
What we offer
What we offer
  • Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
  • Open, transparent culture that includes weekly Town Hall meetings
  • The ability to indirectly or directly change the lives of hundreds of thousands patients
  • Multiple medical benefit options
  • employee premiums paid 100% of select plans, dependents covered up to 80%
  • Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
  • Supplemental fertility benefits coverage
  • Retirement savings program including a 4% Company match
  • Increase paid time off with increased tenure
  • Latest and greatest hardware (laptop, lab equipment, facilities)
  • Fulltime
Read More
Arrow Right

Senior Data Scientist, Care Intelligence

Enable AI product development through data modeling, measurement, and data-drive...
Location
Location
United States
Salary
Salary:
160000.00 - 190000.00 USD / Year
pomelocare.com Logo
Pomelo Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 6+ years professional experience in a data science role with a focus on product development
  • 3+ years professional experience working in healthcare or regulated industries
  • Expert proficiency in both SQL and Python
  • Proven experience with AI product prototyping, leveraging LLMs and model evaluation
  • Passionate about improving maternal health outcomes through innovative AI solutions
  • Demonstrated ability to scope and implement solutions to complex, ambiguous problems across multiple domains
  • Excited to work cross-functionally with technical and non-technical teams, effectively communicating technical capabilities and limitations to diverse stakeholders
Job Responsibility
Job Responsibility
  • Become an expert in Pomelo’s business model and patient experience, identifying opportunities for AI product development
  • Complete exploratory analyses to inform development of AI features, such as conversation topic categorization and patient journey segmentations
  • Contribute to the development of AI-powered features and products, such as content generation, clinical decision support, and automated workflows
  • Define and implement quantitative metrics and measurement frameworks to measure the quality and impact of AI-generated content and workflows
  • Execute comprehensive analyses to measure AI product performance, conduct A/B tests, and quantify the impact of AI-driven features on clinical and business outcomes
What we offer
What we offer
  • Competitive healthcare benefits
  • Generous equity compensation
  • Unlimited vacation
Read More
Arrow Right

Senior Data Scientist - AI Modeling

As a Senior Data Scientist - AI Modeling at Baxter, you will work on creating an...
Location
Location
United States
Salary
Salary:
104000.00 - 143000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree in STEM (science, technology, engineering, math) related field or a similar quantitative analytics field
  • 4+ years of professional experience with a variety of data products / data science model / algorithm development and implementing in production
  • Software development experience
  • Experience with healthcare data and working in a HIPAA regulated environment preferred
  • Experience with varying database structures and large datasets preferred
  • Experience with modern data science tools, such as Spark, Scala, Python, Databricks
  • Experience in Microsoft Azure cloud environment is preferred
  • Proficiency with developing data visualization technology and capabilities (i.e., Power BI, Tableau)
  • Brings a drive for creatively applying pragmatic and scalable approaches to Machine Learning to tackle difficult problems affecting patients and providers
  • Passionate about working on a high-performance team toward a multi-year vision with incremental deliverables
Job Responsibility
Job Responsibility
  • Responsible for the development and implementation of predictive modeling algorithms and techniques to address unmet needs, customer/business problems and optimize user experiences
  • Conduct in-depth research to stay at the forefront of AI advancements, exploring opportunities to integrate predictive and generative AI models into our products and services
  • Predictive and generative AI Modeling
  • Formulate problem statements and hypotheses for diverse business challenges (clinical, operational and business process optimization problems)
  • Create Spark & Python code in Databricks to retrieve data from across disparate data sources and create new innovative actionable insights
  • Prepare data for effective model training
  • Develop, train, and evaluate predictive AI models using various tailored to specific problems
  • Continuously refine and optimize models for performance, scalability, and efficiency
  • Deploy models into production environments and supervise their performance
  • Identify opportunities where generative AI models can add value
What we offer
What we offer
  • Comprehensive medical and dental coverage starting on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident
  • Employee Stock Purchase Plan (ESPP) with discount
  • 401(k) Retirement Savings Plan with employee contributions and company matching
  • Flexible Spending Accounts
  • Educational assistance programs
  • Paid holidays
  • Paid time off ranging from 20 to 35 days based on length of service
  • Family and medical leaves of absence
  • Paid parental leave
  • Fulltime
Read More
Arrow Right
New

Senior Clinical Laboratory Scientist

This position is responsible for performing the complete scope of tests in the l...
Location
Location
United States , Redwood City
Salary
Salary:
63.72 - 79.38 USD / Hour
americannursingcare.com Logo
American Nursing Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelors Of Science, upon hire
  • Clinical Lab Scientist:CA, upon hire or Clinical Microbiology Scientist:CA, upon hire
  • Maintain a valid California License as a Clinical Lab Scientist (CLS)
  • Willingness to actively participate in continue education, competency tests, and attends inservice training seminars to update knowledge and skills
  • Demonstrates knowledge and operation of the Laboratory (LIS) and the Hospital (HIS) computer system
  • Performs and records instrument maintenance, troubleshooting, and quality control including proficiency testing
  • Recognizes and prioritizes tasks appropriately
  • Respond to emergencies, adapt to changing situations and cope with stress in a professional manner
Job Responsibility
Job Responsibility
  • Perform the complete scope of tests in the laboratory section to which assigned
  • Ensure a professional and responsive atmosphere by greeting patients, visitors, staff, and physicians promptly and courteously
  • Validate, record and report tests results via phone, computer entry, and instrument verification protocol in a timely manner
What we offer
What we offer
  • Medical, prescription drug, dental, vision plans, life insurance, paid time off, tuition reimbursement, retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings
  • Parttime
Read More
Arrow Right

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Turkey
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Global clinical trial experience
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
  • Valid driver’s license and passport required
  • Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Job Responsibility
Job Responsibility
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
  • Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Senior Pre-Clinical Scientist within Analytical Chemistry

As one of our pre-clinical chemical analysis scientists, you will become one of ...
Location
Location
Denmark , Humlebæk
Salary
Salary:
Not provided
coloplast.com Logo
Coloplast
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Have a master’s degree or higher with a solid knowledge of organic- and analytical chemistry as well as a broad background in chemistry in general
  • Have a broad knowledge and hand-on experience within methods and equipment’s within the analytical chemical field
  • Have experience working with screening extractables and leachable within ISO 10993
  • Have a good understanding of sample preparation techniques
  • Speak and write English fluently
  • Have a drive to understand complex chemical problems
Job Responsibility
Job Responsibility
  • Become one of our experts in analytical chemistry, supporting projects with your chemical competences
  • Developing and optimizing new analytical methods
  • Helping us understand how our products perform
  • Work on a diverse range of products within wound-, ostomy- and continence care
  • Bring your important chemical knowledge to various cross-functional projects
  • Rethink and help solve unexpected challenges
  • Collaborate closely with cross-functional teams to translate clinical needs into robust analytical chemical protocols
  • Contribute to the scientific foundation of our innovation projects
  • Help guide product development
  • Ensure that our chemical test strategies are aligned with clinical applications
  • Fulltime
Read More
Arrow Right
Jobs by Category
Art and Entertainment Jobs Banking Jobs Call Center Jobs Construction Jobs Consulting Jobs Customer Service Jobs Education Jobs Energy Jobs Finance Jobs Gastronomy Jobs Health and Beauty Jobs Hospitality and Tourism Jobs Human Resources Jobs Insurance Jobs IT - Administration Jobs IT - Software Development Jobs Legal Jobs Logistics Jobs Manufacturing Jobs Marketing, Digital Marketing, SEO, SEM Jobs Media Jobs Nursing Jobs Office Administration Jobs Pharmacy Jobs Physical Work Jobs Public Relations Jobs Public Sector Jobs Purchasing Jobs Quality Control Jobs Real Estate Jobs Research and Development Jobs Sales Jobs
Job Positions Jobs by Country
United States Jobs United Kingdom Jobs India Jobs Canada Jobs Australia Jobs Germany Jobs Ireland Jobs Poland Jobs
Company
Blog About Us Contact
Follow Us
Facebook
X (Twitter)
LinkedIn
Instagram
CrawlJobs Group
ITFlashcards AllDevBlogs
© 2026 CrawlJobs Ltd. All Rights Reserved
Terms & Conditions Privacy Policy