Heidi Lindgreen Holmberg Email & Phone Number

Hovedstaden, Danmark

Hoersholm

Copenhagen Metropolitan Area

Leading cross functional project of strategic value to Chr. Hansen within the Health & Nutrition portfolios. Project maturation and planning: Planning and managing the project from idea to launch, including scoping, target product profile definitions, business case creation in cooperation with commercial experts, go/no-go decisions and post mortem.

Copenhagen Area, Capital Region, Denmark

• Innovator and driver of the scientific field within haemophilia pharmacology with direct and indirect references to the Director of Haemophilia Pharmacology and the Research Project Vice president, respectively
• Device strategies, prioritize resources, evaluate complex data and drive project activities and collaborations across the R&D organisation in my role as project coordinator and scientific coordinator (Clinical.
• Negotiate contracts with consultants and CRO’s
• Daily supervision of 2-3 laboratory technician
• Projects provided with state-of-the-art scientific data necessary for the next major decision and their product development plan
• Mentor for less experienced PhD’s and provide training for subordinates

Copenhagen Area, Capital Region, Denmark

• Project manager, leading 3-4 projects global in a matrix organisation with an average of 20-50 FTE`s and references to the Cooperated Vice President for Research Project
• Establish and execute project strategy and risk management. Subsidise the portfolio strategy within haemophilia
• Budget responsibility for between 200.000 to 5 mill DKK
• Managing project transfer to Clinical Development incl. design of first human trial and process and analysis transfer for scale up to CMC pilot plant
• Initiate and drive international academic and industrial collaborations
• Successful milestone passages in all projects i.e. project approval and/or selection of Research Lead Candidate. Submission of priority applications

Copenhagen Area, Capital Region, Denmark

• Leading global 2-3 projects with an average of 15 FTE`s in the early research phase with direct and indirect references to the Vice President for Haemophilia Pharmacology and the Cooperated Scientific Vice president.
• Establish and execute project strategy and risk management.
• Budget responsibility for between 200.000 to 2 mill DKK
• Initiate and drive international academic and industrial collaborations
• Successful milestone passages or data driven decisions
• Mentor for new project managers

Copenhagen Area, Capital Region, Denmark

• Establishment and implementation of new pharmacological models and assay to support the Haemophilia Research portfolio with direct and indirect references to the Director of Haemophilia Pharmacology and the Cooperated.
• Facilitating a scientific environment securing scientific excellence and environment for new ideas
• Assess scientific data and biology packages for early milestone passage and IRP protection
• Leading global 1-2 projects with an average of 10 FTE`s in the early research phase with direct and indirect references to the Vice President for Haemophilia Pharmacology and the Cooperated Scientific Vice president.
• Approval of two research projects with the associated project plan for establishing proof of principle and identification of research lead compound

Copenhagen Area, Capital Region, Denmark

• Managing strategic cross functional LEAN project within research
• Successfully mapping the activity flow within the biology and pharmacology area from start to hand over to the development organisation. Numerous improvements were identified that increase the effectiveness during.
• Chaired the Animal Ethical Review Committee (11-15 members) at Novo Nordisk A/S for 2½ years, including coordination of the review process with references to the Bioethical Director
• Successful implemented ethical review process of all protocols involving animal studies performed on behalf but outside Novo Nordisk
• Established or refined pharmacological models within the field of cardiovascular diseases, metabolic syndrome and haemostasis in order to test medical hypothesis or new chemical/ biological therapeutics.
• Coordinate research collaborations with academia in EU and US and well as conduction studies at CRO’s

Department Of Preclinical Research

• Managing academic and technical personal (10 FTE’s) at the preclinical research unit
• Daily leader of the animal housing and breeding facility
• Budget responsibility for 7 mill DKK
• Internal consultant for design and execution of in vivo pharmacology studies

Department For Preclinical Research

• Established or refined pharmacological models within the field of cardiovascular diseases
• Study director for studies performed on behalf on external clients
• Internal consultant for designs and execution of in vivo pharmacology studies

Department Of Safety Pharmacology

Industrial PhD student. A collaboration between Novo Nordisk A/S and Faculty of Pharmaceuticals Sciences, Copenhagen University

Department Of Comparative Medicin

Visiting scientist in Dr. JK Williams laboratory, Department of Comparative Medicine.

Dept. Of Pharmacology

Non-clinical/toxicology assessor of pesticides on authorisation applications for the Environmental Protection Agency, including drafting complete letter of response to the applicants

Department Of Biology

• Class room leader of the practical tutorial in physiology for pharmacy students
• Review and feedback on the written reports

Doctor Of Philosophy (Phd), Pharmacology

PhD degree in Pharmacology Dissertation titel:

Master’S Degree, Neuro And Molecular Pharmacology

Masters degree. Dissertation titel:

Master’S Degree, Pharmacy

High School, Matfys