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

New

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

New

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 Pre-Clinical Scientist within Analytical Chemistry

As one of our pre-clinical chemical analysis scientists, you will become one of ...

Location

Denmark , Humlebæk

Salary:

Not provided

Coloplast

Expiration Date

Until further notice

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

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

Scientist I

Scientist I; Onsite, Whitesboro, New York- Full-Time. ICON plc is a world-leadin...

Location

United States , Whitesboro

Salary:

46864.00 - 58580.00 USD / Year

iconplc

Expiration Date

Until further notice

Requirements

Bachelors in Biology, Chemistry, or Biotechnology
Ability to work in a fast paced collaborative environment
Familiarization with basic laboratory operations is preferred
Knowledge of binding assay formats and platforms
Effective communication skills
Attention to detail
Ability to organize and prioritize work

Job Responsibility

Developing and performing assays on biological samples from pre-clinical and clinical trials
Validating the quantification of Biomarkers, New Chemical and Biological Entities in tissues, biological fluids or chemical matrices
Performing assays for routine batch analysis of Biomarkers, NCE and NBE in biological fluids/chemical matrix involving simple to complex analytical techniques
Performing laboratory work to FDA and international regulatory GLP and GCP standards

What we offer

Very competitive salary packages
Annual bonuses
Range of health-related benefits to employees and their families
Competitive retirement plans
Life assurance
Various annual leave entitlements
Global Employee Assistance Programme, LifeWorks
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments

Fulltime

Scientist II

Scientist II- Whitesboro, New York- Full-Time; Onsite. ICON plc is a world-leadi...

Location

United States , Whitesboro

Salary:

56704.00 - 70880.00 USD / Year

iconplc

Expiration Date

Until further notice

Requirements

Bachelors in Biology, Chemistry, or Biotechnology
Ability to work in a fast paced collaborative environment
Familiarization with basic laboratory operations is preferred
Knowledge of binding assay formats and platforms
Effective communication skills
Attention to detail
Ability to organize and prioritize work

Job Responsibility

Under general supervision, develop and perform assays on biological samples from pre-clinical and clinical trials
Validate the quantification of Biomarkers, New Chemical and Biological Entities in tissues, biological fluids or chemical matrices
Perform assays for routine batch analysis of Biomarkers, NCE and NBE in biological fluids/chemical matrix involving simple to complex analytical techniques
Perform laboratory work to FDA and international regulatory GLP and GCP standards

What we offer

Very competitive salary packages
Annual bonuses
Range of health-related benefits to employees and their families
Competitive retirement plans
Life assurance
Various annual leave entitlements
Range of health insurance offerings
Global Employee Assistance Programme, LifeWorks
Flexible country-specific optional benefits

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

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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