Daniela Lupinek Email & Phone Number
Who is Daniela Lupinek? Overview
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Daniela Lupinek is listed as Head of Product Development at LoopLab Bio, a with 19 employees, based in Vienna, Austria. AeroLeads shows a matched LinkedIn profile for Daniela Lupinek.
Daniela Lupinek previously worked as Scientific and Medical Affairs Manager at Looplab Bio (Spin-Out Of Themis Bioscience Ltd.) and Senior Scientist at Themis Bioscience Ltd.. Daniela Lupinek holds Doctor Of Philosophy (Phd), Pharmacology And Toxicology from Universität Wien / University Of Vienna.
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About Daniela Lupinek
With approximately 15 years of professional experience in academia, the pharmaceutical industry, and the biotech sector, I have developed a wide-ranging expertise, including scientific and medical affairs, project management, pre-clinical and clinical research, regulatory affairs and quality control.As a highly effective communicator, I possess a remarkable ability to articulate complex ideas and foster collaborative environments within interdisciplinary teams. I am adept at building strong interpersonal relationships and possess exceptional networking skills, founded on principles of respect, honesty, trust, empathy, and integrity.I am highly appreciated for my reliability, enthusiasm, proactive approach, as well as hands-on mentality, and I consistently deliver exceptional results and drive successful outcomes. I strive for excellence by pro-actively identifying potential issues, seeking innovative solutions, and identifying new opportunities for growth and advancement.
Daniela Lupinek's current company
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Daniela Lupinek work experience
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Scientific And Medical Affairs Manager
• Strategically develop and execute medical affairs strategies that are fully aligned with and supportive of overarching company's overall objectives- Drive external stakeholder engagement and serve as the company's representative to foster collaborations and lead indication selection initiatives- Communicate scientific, medical, and business needs credibly, appropriately, and effectively across a variety of internal and external stakeholders at all levels (e.g., internal… Show more • Strategically develop and execute medical affairs strategies that are fully aligned with and supportive of overarching company's overall objectives- Drive external stakeholder engagement and serve as the company's representative to foster collaborations and lead indication selection initiatives- Communicate scientific, medical, and business needs credibly, appropriately, and effectively across a variety of internal and external stakeholders at all levels (e.g., internal cross-functional meetings, management meetings, company board meetings)- Proactively contribute insights gained from HCP interactions to internal cross-functional teams - Contribute to the development of strategies by communicating my medical insight and knowledge about the disease area, particularly with reference to unmet medical needs and treatment trends - Implement and conduct medical/scientific internal educational meetings- Establish confidentiality agreements, consultancy agreements, and contracts- Organized and oversaw the design and content of LoopLab's homepage and its educational technology video• Conduct extensive and comprehensive literature research:- Identify novel target indications in the field of inflammatory and autoimmune disorders- Stay up-to-date with the latest scientific advancements (e.g. congress participation) and relevant publications in the respective research area- Communicate research findings and propose innovative approaches to facilitate informed decision-making and drive the progress of pipeline development• Develop and compose grant proposals:- Comprehensively outline project objectives, methodologies, and potential impact to secure funding for research initiatives- Successfully secured funding from the Austrian Research Promotion Agency (FFG) for a collaborative research project with University of Natural Resources and Life Sciences (BOKU) Show less
Senior Scientist
• Conducted comprehensive literature research, prepared and performed presentations• Led regular research meetings:- Fostered collaboration and shared knowledge among team members to enhance project progress and outcomes• Managed CROs/Academic collaborators: - Identified and selected contract research organizations (CRO) or academic collaborators to support or perform assay development- Obtained quotes from vendors, CROs, and collaborators- Negotiated prices… Show more • Conducted comprehensive literature research, prepared and performed presentations• Led regular research meetings:- Fostered collaboration and shared knowledge among team members to enhance project progress and outcomes• Managed CROs/Academic collaborators: - Identified and selected contract research organizations (CRO) or academic collaborators to support or perform assay development- Obtained quotes from vendors, CROs, and collaborators- Negotiated prices, made purchases, and ensured timely delivery- Set up confidentiality agreements, consultancy agreements and contracts- Oversaw the logistics and analysis plans for external assays and experiments- Ensured compliance with budget and timelines• Presented and analyzed research data: - Analyzed and interpreted research results - Composed study and project reports- Crafted visually compelling and informative data presentation slides tailored for both internal and external audiences• Served as the representative of the Scientific Affairs department within the Quality Core Team Show less
Senior Scientist
• Participated in productive interactions with the medical agencies (FDA and EMA):- Authored briefing packages (e.g. for PRIME application)- Participated in meetings with representatives from both the FDA and EMA• Proficiently managed Contract Research Organizations and academic collaborations (e.g. Paul-Ehrlich-Institut, Germany, in the course of a CEPI funded project)- Organized and actively participated in routine project status meetings• Oversaw and executed… Show more • Participated in productive interactions with the medical agencies (FDA and EMA):- Authored briefing packages (e.g. for PRIME application)- Participated in meetings with representatives from both the FDA and EMA• Proficiently managed Contract Research Organizations and academic collaborations (e.g. Paul-Ehrlich-Institut, Germany, in the course of a CEPI funded project)- Organized and actively participated in routine project status meetings• Oversaw and executed pre-clinical studies:- Conducted thorough research and evaluation to identify a suitable CRO- Developed comprehensive and robust designs for pre-clinical studies, ensuring adherence to 3Rs and industry best practices• Attended multiple conferences focused on malignant or infectious diseases• Provided scientific support and developed assays:- Trained laboratory technicians to conduct new assays - Designed experiments to support qualification of various assays- Reviewed and discussed relevant literature with other team members- Organized the conduct of in-house experiments with laboratory staff- Assisted in identifying and implementing experimental strategies to support pipeline development- Generated, reviewed, and analyzed experimental data- Analyzed exploratory data by generating graphs using appropriate software tools- Interpreted data in close collaboration with the management team Show less
Research Associate
• Managed and organized three research projects within my doctoral studies titled “Pharmacological potential of cyclodepsipeptides”, ensuring its smooth execution and timely completion• Wrote and published research articles (three as first author)• Presented project data at meetings and conferences• Effectively managed research collaborations, fostering seamless communication and driving successful outcomes• Trained colleagues and undergraduate students in diverse new cell… Show more • Managed and organized three research projects within my doctoral studies titled “Pharmacological potential of cyclodepsipeptides”, ensuring its smooth execution and timely completion• Wrote and published research articles (three as first author)• Presented project data at meetings and conferences• Effectively managed research collaborations, fostering seamless communication and driving successful outcomes• Trained colleagues and undergraduate students in diverse new cell biology methods• Supervised undergraduate students and managed their research projects• Main techniques applied:- Cell culture techniques- Western blot- FACS analysis - RNA isolation- cDNA synthesis- qRT-PCR- Immunofluorescence Show less
Research Technician
• Developed methods for the research project titled “Protein interactions involved in the modulation of the ATRA response by EVI1”• Organized and managed laboratory equipment• Main techniques applied:- Several cell culture techniques- Immunofluorescence staining- RNA isolation/cDNA synthesis/qRT-PCR- Preparation of nuclear extracts- Tandem affinity purification (TAP)- Protein digestion - Stage tip sample purification
Assistant Supervisor
• Scheduled and assigned analytical methods and other tasks in the laboratory• Performed second review and approved test results and QC-relevant documents• Prepared validation plans and reports• Conducted weekly laboratory meetings• Attended meetings on behalf of unit supervisor• Communicated with customers regarding test scheduling and troubleshooting• Supervised and organized analytical method validation and method evaluation
Technician
• Performed diverse analytical methods (HPLC, SDS PAGE with silver or Coomassie Blue staining or WB)• Implemented new HPLC methods, improved and performed the qualification and validation of above listed methods• Implemented new health and environment safety measures• Improved QLP status of the laboratory
Visiting Scientist
• Managed the research project titled “Effects of activated Raf kinase on the nuclear architecture of mammalian cells“ ensuring its smooth execution and timely completion.• Main techniques applied:- Several cell culture techniques- Immunofluorescence staining- Isolation of sub-cellular compartments- 2D SDS PAGE with silver or Coomassie Blue staining, Western blot- MALDI TOF MS, HPLC MS/MS
Daniela Lupinek education
Doctor Of Philosophy (Phd), Pharmacology And Toxicology
Master'S Degree, Toxicology
Education record
Frequently asked questions about Daniela Lupinek
Quick answers generated from the profile data available on this page.
What company does Daniela Lupinek work for?
Daniela Lupinek works for LoopLab Bio.
What is Daniela Lupinek's role at LoopLab Bio?
Daniela Lupinek is listed as Head of Product Development at LoopLab Bio.
Where is Daniela Lupinek based?
Daniela Lupinek is based in Vienna, Austria while working with LoopLab Bio.
What companies has Daniela Lupinek worked for?
Daniela Lupinek has worked for Looplab Bio, Looplab Bio (Spin-Out Of Themis Bioscience Ltd.), Themis Bioscience Ltd., Medical University Of Vienna, and Baxter International Inc..
How can I contact Daniela Lupinek?
You can use AeroLeads to view verified contact signals for Daniela Lupinek at LoopLab Bio, including work email, phone, and LinkedIn data when available.
What schools did Daniela Lupinek attend?
Daniela Lupinek holds Doctor Of Philosophy (Phd), Pharmacology And Toxicology from Universität Wien / University Of Vienna.
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