Pre-Clinical Scientist Job at Coloplast (Humlebæk)

Scientist/Senior Scientist, Vascular

NewLimit is seeking an scientist with experience in endothelial biology to join ...

Location

United States , South San Francisco

Salary:

113000.00 - 171000.00 USD / Year

NewLimit

Expiration Date

Until further notice

Requirements

Ph.D. in cell biology, molecular biology, biochemistry or a related field or equivalent industry experience (5+ years)
Experience with primary endothelial cell isolation and functional characterization
Experience working with mouse models of endothelial cell function (e.g. kidney, cardiovascular, or cognitive disease models)
Experience with transgenic manipulation of endothelial cells either ex vivo or in vivo (e.g. using viral vectors, nucleic acid delivery)

Job Responsibility

Develop functional assays and pre-clinical models to measure endothelial cell function
Collaborate with our Functional Genomics and Predictive Modeling teams to test reprogramming hypotheses at scale
Measure the impact of mRNA reprogramming medicines on endothelial cell function
Engineer in vivo nucleic acid delivery methods for endothelial cells
Analyze and interpret experimental data to drive pre-clinical decision making

What we offer

Health, dental, and vision insurance
401(k) with company match
Paid parental leave
Industry-leading paid time off (PTO) — 20 days/year for all employees + holidays
Meals and snacks on-site

Fulltime

Senior Clinical Scientist

The Senior Clinical Scientist role is suited to scientifically minded candidates...

Location

United States , Salt Lake City

Salary:

Not provided

Blackrock Neurotech

Expiration Date

Until further notice

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

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

Fulltime

Global Development Product Lead

Leads multiple cross functional oncology product teams from pre-clinical candida...

Location

United States , La Jolla; Cambridge; Bothell; South San Francisco; New York City

Salary:

295900.00 - 478800.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

MD or MD-PhD with 10+ years of industry experience in oncology drug development is preferred, track record in oncology clinical research including early phase drug development
Clinical oncology experience: Board certification in oncology preferred
Significant industry leadership experience in clinical, translational or basic research in biomedical sciences or one of the disciplines related to drug development
Understanding of related disciplines (e.g., biostatistics, regulatory, pre-clinical pharmacology, pharmaceutical sciences)
Demonstrated scientific productivity (publications, abstracts, etc.)
Proven scientific writing skills and good communication skills
Proven leadership skills with ability to defend the clinical plan at governance meetings is essential
Capacity to adapt to a fast-paced and changing environment
Demonstrated history of effective leadership
including cross functional and matrixed teams, managing direct reports when applicable, and experience in seeking and maintaining alignment with cross-functional leaders

Job Responsibility

Leads multiple (~2-4) cross functional oncology product teams from pre-clinical candidate nomination (CAN) through Phase 1-2 clinical development and proof of concept (POC) stages
In close collaboration with functional experts on the product teams, drives the effective integration of an end-to-end cross functional molecule strategy and risk mitigation plan and ensures delivery of data-driven milestones through successful risk identification and mitigation
Support clinical trials and the development strategy for early development assets and lead development programs across multiple functions within Pfizer Oncology, as well as represent the program with the external clinical community
Develop clinical development plan from first in human clinical trial to proof-of-concept, including assessment of appropriate combinations, as well as evaluation of potential predictive and pharmacodynamics biomarker plans
To ensure the cross-functional components of the product plans including clinical expertise are provided to project teams, including medical monitoring of clinical trials
Substantial support of CDP development and diligence for external innovation activities
Lead key enterprise level cross-functional workstreams to accelerate R&D decision making
Lead, develop and execute strategic development for early development assets
Ensure timely execution and delivery of product milestones within budget
Communicate with executive management and governance committees to address program needs and provide recommendations

What we offer

Participation in Pfizer’s Global Performance Plan with a bonus target of 30.0% of the base salary
Eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Relocation assistance may be available based on business needs and/or eligibility

Fulltime

Senior Research Scientist (Pre-clinical) - 4DBio³ ODB

The Senior Research Scientist (Pre-clinical) serves as a scientific lead for pre...

Location

United States , Rockville

Salary:

135000.00 - 155000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

Ph.D. in a relevant field (e.g., biology, pathology, biochemistry, bioengineering, molecular and cell biology, or genetics) required
3-5 years’ experience with planning and management of innovative medical and/or scientific research programs
Minimum 8 years direct experience in hematopoiesis research such as cell culture and differentiation of stem cells and/or synthetic blood substitutes
Experience with multi-color flow cytometry and cell sorting
Experience with blood cell function assays
Experience with gene editing and molecular biology techniques
Ability to design and execute in vitro experiments
Experience and success in writing and receiving federal research grants, cooperative agreements, and/or contracts
Experience working in DoD or other Federal research environments
Experience supervising research personnel

Job Responsibility

Perform recurring analyses on research portfolios to identify critical gaps, exceptional results and/or lack of progress
Assist in the preparation of SOPs and analysis of laboratory experiments
Prepare interim and final progress reports
Ensure research integrity
Disseminate research results
Provide guidance to scientists preparing research proposals, to include guidance on research protocol development, as needed
Maintain open communication with Principal Investigators and Center Leadership, advises of processes, reports progress, and serves as a point of contact, as applicable
Perform scientific reviews on research proposals submitted for consideration, as requested
Direct multifunctional teams and provides scientific domain expertise as needed
Adhere to Occupational Safety and Health Administration (OSHA), Good Laboratory Practices (GLP) and infection control procedures, as applicable

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year
up to 4 weeks of paid time off in a rolling year

Fulltime

Research Scientist II - Toxicologist

Lead in ensuring product compliance and patient safety through cutting-edge toxi...

Location

United States , Round Lake

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

BS with 8+ years, MS with 6+ years, or PhD with 2+ years of relevant experience in R&D and/or GLP environments
Medical Device experience strongly preferred
Solid understanding of national and international non-clinical safety and biological evaluation regulations, including Good Laboratory Practices (GLP)
Direct experience working with regulatory bodies such as the US-FDA, EU Notified Bodies, and other national or international reviewers
A strong track record of presenting at scientific conferences and authoring/co-authoring published articles in peer-reviewed journals
Demonstrated ability to advance new product development projects and provide innovative non-clinical solutions for pharmaceutical and medical device challenges
Experience in a GLP and/or R&D environment, with a solid understanding of project management principles

Job Responsibility

Provide technical and strategic input to project teams
Take the lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments
Plan and manage complex projects
Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
Support innovation initiatives by providing technical direction
Participate in standards organizations and regulatory committees
Work closely with R&D, Clinical, Medical Affairs, Regulatory Affairs, Quality, Manufacturing, and Environmental Health and Safety teams
Articulate the Pre-Clinical Toxicology vision, goals, and performance to project teams
Establish and nurture professional networks both internally and externally

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Senior Research Scientist - Toxicologist

Lead in ensuring product compliance and patient safety through cutting-edge toxi...

Location

United States , Round Lake

Salary:

144000.00 - 198000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

BS with 12+ years, MS with 10+ years, or PhD with 4+ years of relevant experience in R&D and/or GLP environments
Medical Device experience strongly preferred
Solid understanding of national and international non-clinical safety and biological evaluation regulations, including Good Laboratory Practices (GLP)
Direct experience working with regulatory bodies such as the US-FDA, EU Notified Bodies, and other national or international reviewers
A strong track record of presenting at scientific conferences and authoring/co-authoring published articles in peer-reviewed journals
Demonstrated ability to advance new product development projects and provide innovative non-clinical solutions for pharmaceutical and medical device challenges
Experience in a GLP and/or R&D environment, with a solid understanding of project management principles

Job Responsibility

Provide technical and strategic input to project teams, ensuring compliance with Baxter and external standards while driving business objectives
Take the lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments, to support global programs
Plan and manage complex projects, prioritizing workloads and meeting major organizational objectives in collaboration with senior management
Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
Support innovation initiatives by providing technical direction and ensuring the quality of deliverables that integrate state-of-the-science theory with practical approaches
Participate in standards organizations and regulatory committees to influence emerging regulations based on sound scientific principles
Work closely with R&D, Clinical, Medical Affairs, Regulatory Affairs, Quality, Manufacturing, and Environmental Health and Safety teams to support various projects and initiatives
Articulate the Pre-Clinical Toxicology vision, goals, and performance to project teams, fostering a culture of high standards and stretch goals
Establish and nurture professional networks both internally and externally, participating in global task forces and committees to exchange technical information

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

Senior Research Scientist - Toxicologist

Lead in ensuring product compliance and patient safety through cutting-edge toxi...

Location

United States , Round Lake

Salary:

144000.00 - 198000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

BS with 12+ years, MS with 10+ years, or PhD with 4+ years of relevant experience in R&D and/or GLP environments
Medical Device experience strongly preferred
Solid understanding of national and international non-clinical safety and biological evaluation regulations, including Good Laboratory Practices (GLP)
Direct experience working with regulatory bodies such as the US-FDA, EU Notified Bodies, and other national or international reviewers
A strong track record of presenting at scientific conferences and authoring/co-authoring published articles in peer-reviewed journals
Demonstrated ability to advance new product development projects and provide innovative non-clinical solutions for pharmaceutical and medical device challenges
Experience in a GLP and/or R&D environment, with a solid understanding of project management principles

Job Responsibility

Provide technical and strategic input to project teams, ensuring compliance with Baxter and external standards while driving business objectives
Take the lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments, to support global programs
Plan and manage complex projects, prioritizing workloads and meeting major organizational objectives in collaboration with senior management
Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
Support innovation initiatives by providing technical direction and ensuring the quality of deliverables that integrate state-of-the-science theory with practical approaches
Participate in standards organizations and regulatory committees to influence emerging regulations based on sound scientific principles
Work closely with R&D, Clinical, Medical Affairs, Regulatory Affairs, Quality, Manufacturing, and Environmental Health and Safety teams to support various projects and initiatives
Articulate the Pre-Clinical Toxicology vision, goals, and performance to project teams, fostering a culture of high standards and stretch goals
Establish and nurture professional networks both internally and externally, participating in global task forces and committees to exchange technical information

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

Senior Research Scientist - Toxicologist

Lead in ensuring product compliance and patient safety through cutting-edge toxi...

Location

United States , Round Lake

Salary:

144000.00 - 198000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

BS with 12+ years, MS with 10+ years, or PhD with 4+ years of relevant experience in R&D and/or GLP environments
Medical Device experience strongly preferred
Solid understanding of national and international non-clinical safety and biological evaluation regulations, including Good Laboratory Practices (GLP)
Direct experience working with regulatory bodies such as the US-FDA, EU Notified Bodies, and other national or international reviewers
A strong track record of presenting at scientific conferences and authoring/co-authoring published articles in peer-reviewed journals
Demonstrated ability to advance new product development projects and provide innovative non-clinical solutions for pharmaceutical and medical device challenges
Experience in a GLP and/or R&D environment, with a solid understanding of project management principles

Job Responsibility

Provide technical and strategic input to project teams, ensuring compliance with Baxter and external standards while driving business objectives
Take the lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments, to support global programs
Plan and manage complex projects, prioritizing workloads and meeting major organizational objectives in collaboration with senior management
Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
Support innovation initiatives by providing technical direction and ensuring the quality of deliverables that integrate state-of-the-science theory with practical approaches
Participate in standards organizations and regulatory committees to influence emerging regulations based on sound scientific principles
Work closely with R&D, Clinical, Medical Affairs, Regulatory Affairs, Quality, Manufacturing, and Environmental Health and Safety teams to support various projects and initiatives
Articulate the Pre-Clinical Toxicology vision, goals, and performance to project teams, fostering a culture of high standards and stretch goals
Establish and nurture professional networks both internally and externally, participating in global task forces and committees to exchange technical information

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

Pre-Clinical Scientist

Coloplast

Location:
Denmark , Humlebæk

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 09, 2026

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