Lead Clinical Laboratory Scientist Jobs

New

Lead Clinical Laboratory Scientist (CLS), Oncology

Join a team of brilliant, passionate innovators who wake up every day determined...

Location

United States , Menlo Park

Salary:

228788.00 USD / Year ▼

BillionToOne

Expiration Date

Until further notice

Requirements

Bachelor's degree in the chemical, physical or biological sciences
Minimum of 4 years of CLS experience in a clinical setting (molecular and/or high-complexity laboratory experience preferred)
A current California Clinical Laboratory Scientist License that meets requirements for Testing Personnel under CLIA regulations (42 CFR, part 493) (ASCP, CGMBS or generalist license is required)
Hands-on training and experience with manual molecular biology protocols, including DNA extraction, PCR, and automated liquid handlers
Advanced knowledge of Google Docs, Word, Excel, basic statistics and familiarity with LIMS systems and Next-Generation Sequencing
Strong attention to detail and ability to work flexibly and well under given timeframes.
Self-starter and dynamic team player with excellent verbal and written skills.

Job Responsibility

Lead clinical laboratory daily supervision in alignment with company values and mission
Hold General Supervisor delegation and responsibilities including oversight and support of day-to-day operations, scheduling, and troubleshooting
Manage CLIA direct reports including licensed and/or unlicensed staff (CLS, Clinical Laboratory Assistants)
Contribute to continuous process improvement projects including tech transfer, troubleshooting, training, and validations
Perform clinical laboratory assays to provide data for diagnosis, treatment, and prevention of disease
Perform quality control studies to ensure the accuracy of clinical data
Verify instrument performance by checking and calibrating specific lab instruments and documents data

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

New

Intern, Cytometry Shared Resource Lab

The BioMarin Summer Internship Program will enable students to gain valuable exp...

Location

United States , San Rafael

Salary:

24.00 - 32.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Undergraduate or Masters Candidate pursuing a degree in biochemistry, cell biology or equivalent, with an interest in a laboratory career preferred
Must be currently enrolled as a full-time student at an accredited U.S. based university or college and enrolled in the fall term after the completion of the internship OR have graduated within 1 year of the start of the program
Must be available to work full-time, 40 hours a week
Must be able to relocate if necessary and work at the designated site for the duration of the internship for on-site, hybrid roles
Required Coursework: Molecular Biology and Molecular Biology Laboratory or equivalent courses
Cell Biology or Molecular Immunology or equivalent courses
Cell Biology Laboratory or Molecular Immunology Laboratory or equivalent courses

Job Responsibility

Working with the Lead Scientist and Research Associates in the Cytometry Core within the Center of Technology
Gain knowledge of how flow cytometry, high content imaging and cell sorting are used in a biotechnology environment to support research, bioanalysis, and clinical work
Gain knowledge in how to operate a flow cytometer, high content imager and cell sorter
Receive training in a typical flow cytometry assay including complex options for data analysis
Gain experience in a Shared Resource Laboratory (SRL or Core Lab) touching many parts of the drug discovery process

What we offer

Apply skills and knowledge learned in the classroom to on-the-job experiences
Comprehensive, value-added project(s)
Work in teams and with colleagues in a professional environment
Develop skills specific to your major
Opportunities for professional development by building relationships and learning about other parts of the business
Participate in company all hands meetings, monthly community lunches
Corporate office amenities such as: 24/7 on-site gym, coffee truck, snacks
Access to Employee Resource Groups

Fulltime

Scientific Associate Director - Pharmacokinetics and Drug Metabolism

In this vital and exciting role, you will oversee Pharmacokinetics and Drug Meta...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

PhD in Pharmacokinetics, Pharmaceutical Sciences, Engineering, or related fields with equivalent professional degrees and 12+ years of experience in the Biotechnology/Pharmaceutical Industry
Solid technical experience with the application of SM in vitro/in vivo ADME and pharmacokinetics fundamentals to drug discovery projects
Ability to drive the progression of SM discovery and development within project teams
Expertise with in vitro ADME, in vivo ADME, PK/PD etc
Experience in supporting preclinical components of regulatory documentations
Excellent interpersonal, technical, and communication skills
Past experience as a laboratory scientist in a pharma or biotech environment
Excellent written and oral communication skills, attention to detail and accuracy, and interpersonal skills
Record of scientific contributions through peer-reviewed articles and external presentations

Job Responsibility

Lead/mentor a team of scientists involved in ADME characterization of small molecules
Directly responsible for leading a team of scientists involved in undertaking mechanistic in vitro ADME assays
Develop/implement novel tools to efficiently support mechanistic ADME work
Oversee activities/establish workflows for small molecule bioanalytical and ADME screening teams
Serving as a subject matter expert of small molecule ADME to support the programs and recommend strategies to PKDM project team representatives to reduce/mitigate risks due to metabolism
Collaborate with scientists across our PKDM scientific community
Leveraging specialized ADME/PK skills such as in vitro ADME, in vivo ADME, biotransformation, PK/PD, to impact project progression and decision-making
Contributing to the analysis of pre-clinical ADME and PK data for IND and NDA filings and documenting these analyses in appropriate reports
Building close relationships with partner functions

Nephrology Transplant Physician Scientist

Hackensack Meridian Health is seeking a Nephrology Transplant Physician Scientis...

Location

United States , Hackensack

Salary:

198930.00 USD / Year

American Society of Transplantation

Expiration Date

Until further notice

Requirements

MD or equivalent foreign degree
Completion of an Internal Medicine Residency and Transplant Fellowship
Consideration for applicants with strong transplant experience during/after a Nephrology Fellowship
Minimum 3 years in a funded research program
Demonstrated success securing NIH and/or foundation funding
Peer-review experience (manuscripts, grants, editorial boards, or review committees)
Minimum of 15 scientific publications, with majority as first or last author
Board Certified in Internal Medicine
Board Certified or Board Eligible in Nephrology
Eligible for New Jersey Medical License

Job Responsibility

Conduct impactful basic or translational research in transplant/immunology
Pursue grant funding and philanthropic support to sustain laboratory operations
Lead and oversee laboratory processes, research staff, budgeting, and financial management
Establish strategic research goals aligned with the clinical goals of the Division of Organ Transplantation
Hold regular oversight meetings with the Chief Scientific Officer and Director of Transplantation
Develop and implement laboratory policies, procedures, and personnel decisions
Mentor and evaluate lab staff performance
Participate in professional activities, including consulting, editorial work, training, study sections, seminars, and national/international conferences
Evaluate potential living donor and transplant recipient candidates
Provide inpatient and outpatient care for pre- and post-transplant donors and recipients

What we offer

health, dental, vision, paid leave, tuition reimbursement, and retirement benefits

New

Scientist II, In Vivo, Enzymatic and Metabolic Therapeutic Area

The Scientist will join the Enzymatic and Metabolic In Vivo team to design and e...

Location

United States , Petaluma, CA

Salary:

116000.00 - 159500.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

PhD in a related subject area with demonstrated in vivo research experience in metabolic disease
Postdoctoral or industry (2-5 years preferred) experience in genetic metabolic diseases
Extensive hands-on experience with rodent in vivo work in the metabolic field
Demonstrated experience in metabolic biology/disease research in academia or industry (preferred) including publication record
Strong analytical, problem-solving, and decision-making skills
Strong understanding of genetically engineered models, breeding, and management and Gene therapy modalities
Excellent oral and written communication skills
Passion for contributing your scientific skills to develop therapies for patients in need
Must be able to utilize computer databases for analysis, data entry, and point of care observations
Must be able to work under time constraints with minimal direction of day-to-day responsibilities, including collaboratively working with multidisciplinary teams

Job Responsibility

Conduct research on genetic metabolic diseases
Contribute to novel therapeutic programs based on innovative, ground-breaking discoveries that could lead to new, high-impact opportunities for patients
Perform research and publish findings in high-impact journals and present research at major conferences
Effectively partner with other scientists and the Research and Early Development team to develop and execute on the program's strategic plan
Present program data at a range of internal forums, including project team meetings, Research Department Seminars and Research leadership governance forums
Write, review and contribute to study synopses, protocols, study reports and regulatory documents
Collaborate with various BioMarin functions, CROs, university or analytical laboratories, business partners, as necessary to ensure appropriate/timely progression of projects
Participate in multi-disciplinary drug development teams and may lead sub-teams
Execute hands-on responsibilities including but not limited to animal handling and restraint (rodents), administration via various routes of administration, including intravenous (tail-vein), in-life animal health monitoring and measurements, clinical observations, sample collection and processing, and accurate data collection
Provide daily care and monitoring of mice or rats, including health checks and documentation

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

New

Certified Nursing Assistant

Are you looking for a career where you are valued, supported and encouraged? At ...

Location

United States , Chelsea

Salary:

Not provided

Deutsches Altenheim

Expiration Date

Until further notice

Requirements

Certification as a CNA
Determine Resident’s needs in a timely manner
Provide Residents with outstanding care (customer service)
Assist Residents with grooming, bathing, oral hygiene, personal care, toileting, meals/feeding, etc.
Assists Residents with going short distances around the building
Be willing to respond to other duties as assigned

What we offer

Company sponsored trip to Encore Casino or Great Wolf Lodge after 3 years of employment
Free company grocery store – estimated at over $100 worth of groceries a week
Free meals every day
Rewarding job within an outstanding and recognized organization
Great working environment in our state-of-the-art facility located on Admirals Hill
Health, Dental and Vision Insurance
Basic Life Insurance
Voluntary Insurance (Accident, LTD, STD, Whole Life Insurance)
403(b) Retirement Plan
Shift Differentials

New

Paramedic

Every day, the donors you meet will motivate you. The high-quality plasma you co...

Location

United States , Bossier City

Salary:

22.69 - 31.20 USD / Hour

BioLife Plasma Services

Expiration Date

Until further notice

Requirements

High school diploma or equivalent to including graduate equivalent of a recognized educational nursing program with state requirements
Currently licensed or certified in the state where responsibilities will be assigned: EMT-Paramedic
Current Cardiopulmonary Resuscitation (CPR) and AED certification
Fulfill state requirements (in state of licensure) for basic IV therapy
Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist
Two years in a clinical or hospital setting

Job Responsibility

Determine donor eligibility to donate plasma
Management of donor adverse events
Review of laboratory test results
Donor notification of unsuitable test results
Determine donor eligibility
to include, proper management of informed consent, AIDS education and confidential self-exclusion, medical history interview and acceptance requirements, physical examination, blood testing, and reviewing Serological Protein Electrophoresis (SPE)
Evaluate donor reaction(s), which occurs at the facility as outlined in the SOPs
Follow applicable SOPs for medical emergencies including the development of Center Physician's standing orders and donor transport to emergency care facilities
Refer to the Center Physician or Medical Affairs (as applicable) when in need of providing unacceptable findings to donors, or guidance concerning medical or technical issues, including donor safety and eligibility
Support the Hepatitis B and Seasonal Flu vaccination programs for employees as applicable

What we offer

Medical Benefits an Full Vacation starting day one
$3000 Sign-On Bonus Available
Medical, dental, vision insurance
401(k) plan and company match
Short-term and long-term disability coverage
Basic life insurance
Tuition reimbursement program
Paid volunteer time off
Company holidays
Well-being benefits

Fulltime

New

Gvp compliance lead

BioMarin is looking for an individual with experience working in Pharmacovigilan...

Location

United States

Salary:

176000.00 - 242000.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

10+ years of experience working within a regulated healthcare industry including a role in capacity of quality and compliance
Working knowledge of FDA, EMA, and global PV Regulations, and application of Good Pharmacovigilance Practices (GVP), ICH and GCP regulations
Experience working in Pharmacovigilance (PV) within Quality and Compliance
Experience executing or managing Health Authority Inspections
Experience executing or managing R&D Audits and GVP Audit Program
Experience with identifying optimal strategy for executing a GVP audit program working with internal auditors and external consultants
Experience navigating and understanding a quality management system
Core leadership competencies in strategic thinking, agility, prioritization, communication and decision making
Experience in managing staff and leading teams
Strong verbal, written and oral communication skills. Able to present to Senior Leadership.

Job Responsibility

Championing the implementation of Global Quality vision, policies, processes, and decisions
Collaborate with stakeholders to identify, communicate, and mitigate compliance risks
Continually enhance partnerships with key stakeholders and leaders across the business
Support and drive the implementation of quality and compliance projects and objectives
Stay updated on regulations and recommend proactive compliance changes when necessary
Develop and enhance GVP Compliance processes and best practices
Lead the execution of the GVP Compliance Global Audit Program
Act as a GVP compliance core team member on regulatory inspection teams and support mock readiness activities
Provide insights to continually optimize the GVP Compliance Audit Program
Contribute to Pharmacovigilance System Master File (PSMF) updates

What we offer

company-sponsored medical, dental, vision, and life insurance plans
discretionary annual bonus
discretionary stock-based long-term incentives
paid time off

Fulltime

Lead Clinical Laboratory Scientist

BillionToOne

Location:
United States , Union City

Category:
Health and Beauty

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 26, 2025

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