Anna Dahlman
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Anna Dahlman Email & Phone Number

Director, Non-Clinical Safety and Toxicology at Genmab
Location: Copenhagen, Capital Region Of Denmark, Denmark 12 work roles 3 schools
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Role
Director, Non-Clinical Safety and Toxicology
Location
Copenhagen, Capital Region Of Denmark, Denmark
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Who is Anna Dahlman? Overview

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Anna Dahlman is listed as Director, Non-Clinical Safety and Toxicology at Genmab, a company with 2607 employees, based in Copenhagen, Capital Region Of Denmark, Denmark. AeroLeads shows a matched LinkedIn profile for Anna Dahlman.

Anna Dahlman previously worked as Director, Non-Clinical Safety & Toxicology at Genmab and Associate Director, Non-Clinical Safety & Toxicology at Genmab. Anna Dahlman holds Phd, Medical Science from Lund University.

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Genmab

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Profile bio

About Anna Dahlman

Toxicologist with broad experience in pharmaceutical drug development within oncology, immune-oncology and immunology. Extensive hands-on experience with target identification, early proof of concept, hazard identification and risk assessment, safety and toxicity studies, IND/CTA/IMPD submissions, pre-IND and scientific advice meetings, and early clinical development. Lead nonclinical safety scientist for 5 successful CTA/IND/IMPDs and contributed scientifically to additional submissions. Advocate for advancing new alternative methods (NAM) to improve safety assessments and to reduce the use of animals in research. Personal strengths include excellent communication and organizational skills combined with a good sense of humor.

Listed skills include Cell Biology, Antibodies, Cell, Cancer Research, and 19 others.

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Genmab
Genmab
Director, Non-Clinical Safety and Toxicology
Copenhagen, DK
Website
Employees
2607
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12 roles

Anna Dahlman work experience

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Director, Non-Clinical Safety And Toxicology

Copenhagen, DK

Director, Non-Clinical Safety & Toxicology

Current

Copenhagen Metropolitan Area

Oct 2023 - Present

Associate Director, Non-Clinical Safety & Toxicology

Copenhagen Area, Denmark

  • Develop and execute nonclinical safety evaluations strategies based on intended pharmacologic effect, therapeutic indication and international guidelines and best practice.
  • Design, monitor, interpret and report nonclinical safety and toxicity studies conducted at CROs.
  • Represent non-clinical safety on cross functional global development teams.
  • Develop and manage timelines for external and internal deliverables for CTA/IND enabling documents. Initiate and lead subteams. Ensure justification of the preclinical species.
  • Author non-clinical safety sections of IND/CTA/IMPDs. Represent nonclinical safety in authority interactions such as scientific advice and pre-IND meetings.
  • For compounds in clinical development, review DSURs and functional representative in Safety committee meetings.
Oct 2019 - Oct 2023

Senior Scientist, Preclinical Safety

Lund, Sweden

  • Responsible for planning and conducting nonclinical safety and toxicology studies supporting the development of therapeutic antibodies in immuno-oncology, including three successful CTA submissions.The role included a.
  • Evaluation of new CROs, request for proposals, site visits, and scientific support at audits
  • Planning study dates, requesting study quotes, managing contracts
  • Managing the budget for the nonclinical studies
  • Designing, monitoring, and interpreting results from nonclinical toxicology studies (non-GLP and GLP; in vitro and in vivo), with consideration to pharmacological mode-of-action, and ensuring regulatory compliance
  • Prepare nonclinical toxicology sections in clinical trial application documents (IB and Clinical study protocol).
Oct 2017 - Sep 2019

Scientist

Lund, Sweden

As a scientist at Alligator Bioscience, my role was to be the Preclinical Safety Lead for three drug development projects at Alligator Bioscience. The projects involve therapeutic antibodies, bispecific and monoclonal, for use as tumor targeted immune activating compounds in cancer patients. In a small sized company as Alligator, the role as Preclinical.

Jan 2016 - Sep 2017

Scientific Writer (Project Assignment)

Faculty Of Medicine

Organizing and compiling the experiences from a pilot test of the new national clinical guideline for palliative care (Nationell Vårdplan för Palliativ vård, NVP). Authored the case study paper 'A novel care guide for personalized palliative care - a national initiative for improved quality of care' published in BMC Palliative Care.

Sep 2015 - Dec 2015

Research Scientist

Copenhagen Area, Denmark

In my role as a Scientist in the Department for Preclinical Pharmacology and Toxicology, I provided expertize in cell-based assays for drug discovery and development. I designed, performed, and analyzed in vitro experiments for mode-of-action studies and anti-tumor efficacy through to IND. Set up and evaluation of biomarkers for efficacy and tissue-cross.

Jun 2011 - May 2015

Postdoctoral Scientist

Faculty Of Medicine

Mar 2011 - May 2011

Phd Medical Sciences

Faculty Of Medicine

During my doctoral studies I investigated the potential role of MSMB and CRISP-3 as prognostic biomarkers for prostate cancer progression. This included manual and automated immunohistochemical analysis of prostate cancer tissue from patients, as well as a wide range of laboratory techniques characterizing gene and protein expression, cell culture, small.

Nov 2006 - Feb 2011

Visiting Researcher

Cancer Research Unit, York University, Yorkshire, UK

Technical and methodological training in sorting subpopulations of cells from primary prostate cancer tissue, based on their difference in morphology and surface receptors.

May 2007 - Jun 2007

Summer Intern

In teh Department of Laboratory Medicine, Division of Molecular Medicine, I studied how arsenic trioxide can induce differentiation and cell death in neuroblastoma tumor cells.

Jun 2005 - Jul 2005

Summer Intern

In the Department for Cell and Organism Biology, Division of Molecular genetics, I worked on characterizing genetic control of telomerase length in Saccharomyces yeast cells.

Jun 2004 - Jul 2004
Team & coworkers

Colleagues at Genmab

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3 education records

Anna Dahlman education

Phd, Medical Science

Lund University

Activities and Societies: Representative at the Department board (2007-2008), board member of the Medical PhD council (2009-2011), member.

Master'S Degree, Medicine

Thesis title: Arsenic Trioxide Induced Cell Death in Multidrug Resistant Neuroblastoma Cells: Expression Pattern of Selected Genes

Bsc, Biology

Activities and Societies: Board member of Friskis&Svettis, Växjö. In charge of the 'Members Section', responsible for all communication to.

FAQ

Frequently asked questions about Anna Dahlman

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What company does Anna Dahlman work for?

Anna Dahlman works for Genmab.

What is Anna Dahlman's role at Genmab?

Anna Dahlman is listed as Director, Non-Clinical Safety and Toxicology at Genmab.

Where is Anna Dahlman based?

Anna Dahlman is based in Copenhagen, Capital Region Of Denmark, Denmark while working with Genmab.

What companies has Anna Dahlman worked for?

Anna Dahlman has worked for Genmab, Alligator Bioscience Ab, Lund University, Symphogen, and University Of York.

Who are Anna Dahlman's colleagues at Genmab?

Anna Dahlman's colleagues at Genmab include Larisa Hubbs, Ccep, Elizabeth Kephart Kuczkowski, Parth Zalawadia, Karen Banda, Mba, and Anette Allentoft.

How can I contact Anna Dahlman?

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What schools did Anna Dahlman attend?

Anna Dahlman holds Phd, Medical Science from Lund University.

What skills is Anna Dahlman known for?

Anna Dahlman is listed with skills including Cell Biology, Antibodies, Cell, Cancer Research, In Vitro, Cell Culture, Cancer, and Immunohistochemistry.

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