Dr. Marta Stolarczyk

Dr. Marta Stolarczyk Email and Phone Number

Principal Medical Science Liaison covering EU (R and D - Medical Affairs - EU) @ X4 Pharmaceuticals
Heidelberg, BW, DE
Dr. Marta Stolarczyk's Location
Heidelberg, Baden-Württemberg, Germany, Germany
Dr. Marta Stolarczyk's Contact Details

Dr. Marta Stolarczyk work email

Dr. Marta Stolarczyk personal email

About Dr. Marta Stolarczyk

I am passionate scientist with the scope of interest in translational research with expertise in oncology and pulmonology. During my PhD at ErasmusMC Rotterdam (top Clinical Research Center in the Netherlands) I investigated inflammatory responses in Cystic Fibrosis and COPD using advanced patient cell-based lung models. My project was conducted in collaboration with researchers from different European and non-European countries (the Netherlands, Germany, Canada), therefore I learned how to build long term international business partnerships. During the period of my PhD I had opportunity to participate in many international conferences as a presenter (The Netherlands, Italy, France, US). I was participating in the regular lung meetings with clinicians, translational researchers and pharmaceutical business partners in Rotterdam, Leiden and Utrecht Clinic.In order to become more independent researcher, I decided on the Postdoc position at Heidelberg Uni Clinic, where I established the foundation for the microscopy based drug testing platform as well as implemented the first single cell sequencing into the clinical practice for patients with lymphoma and leukemia (including DLBCL, FL, CLL). I helped to equip and set up the newly arising laboratory (including purchase of the confocal high throughput microscope for Heidelberg Uni Clinic) and shape the basis for further research. This challenging position helped me to develop high independence in terms of project planning, project management and staff management. Close collaborations with clinicians and researchers from different institutions (Heidelberg Uni Clinic, EMBL, DKFZ, Hannover University) taught me how to communicate with medical doctors, nurses and scientists having expertise in various fields (biostatisticians, chemists, basic researchers). Site management associate position gave me insides into the clinical trial management on the sites. I got familiar with clinical trial operations, European clinical regulations and ICH-GCP. I have high interest in clinical research trials, but I am also passionate about translational oncology, inflammatory responses, NGSeq, SingleCellSeq, diagnostic, data science. I am good team player as well as lead with the proven skills in project and staff management. I have good skills in presenting and transferring scientific knowledge to staff with different background. If you are interested in getting in touch with me, please send me an email: stolarczyk.marta@gmail.com

Dr. Marta Stolarczyk's Current Company Details
X4 Pharmaceuticals

X4 Pharmaceuticals

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Principal Medical Science Liaison covering EU (R and D - Medical Affairs - EU)
Heidelberg, BW, DE
Website:
x4pharma.com
Employees:
111
Dr. Marta Stolarczyk Work Experience Details
  • X4 Pharmaceuticals
    Principal Medical Science Liaison Covering Eu (R And D - Medical Affairs - Eu)
    X4 Pharmaceuticals
    Heidelberg, Bw, De
  • Novocure
    Clinical Scientist Lead (Emea, Clinical Development)
    Novocure
    Heidelberg, Bw, De
  • Novocure
    Clinical Scientist Lead (Clinical Development)
    Novocure Mar 2022 - Present
    Root, Switzerland, Ch
    Scientific and strategic lead on a global clinical trial conducted in Europe, US and China(Successful delivery of the study)-cross-functional team management to deliver top line data in a timely manner for one of the global clinical trial (together with Medical Director)
  • Novocure
    Clinical Research Scientist (Clinical Development)
    Novocure Jan 2021 - Present
    Root, Switzerland, Ch
    - relationship development with Key Opinion Leaders (KOLs) and Principal Investigators (PIs) in various countries: Germany, Poland, Netherlands and Belgium- exchange of the scientific knowledge with KOLs during various conferences (ESMO, ASCO, AACR. etc) and site visits- be on top of knowledge regarding following entities of cancers: NSCLC, Brain Metastasis, Pancreatic and Hepatic cancer, Ovarian cancer- feedback collection from PIs regarding Clinical Trial Protocol and implementation of Protocol Amendments - development of Clinical Trial strategy for start-up, recruitment and top line data delivery in close collaboration with Medical Director - management of patient enrollment and assurance that the patient eligibility criteria are met (acting as the right hand of medical director for European countries)- assurance the integrity of the clinical study data, assessment of protocol deviations and other medical issues - strong collaboration with Clinical Operators to support start-up activities, new site selection and support for operational activities on the open sites (including vendor management) - medical monitoring and data cleaning with strong collaboration with Medical Director, Clinical Operations Manager, Data Manager and Biostatics Manager- collaboration with Medical Affairs department on organization of webinars and other educational events for professionals (KOLs/PIs/side staff)
  • Pra Health Sciences
    Site Management Associate, Real World Solutions
    Pra Health Sciences Jan 2019 - Dec 2020
    Raleigh, North Carolina, Us
    - Implementation and monitoring of phase 3 and post-marketing studies to ensure sponsor in and investigator obligations are met and are compliant with applicable local regulatory requirements and ICH guidelines (projects for different sponsors: BMS, AstraZeneca, Roche and others)- Recruitment and evaluation of potential sites for participation in the late phase studies. - In-house site management that encompass: 1) clinical study tracking to ensure that the study files are current, accurate, and complete 2) collection, review, maintenance of essential document 3) close out activities4) liase with external clients and authorities to ensure adherence to the late phase study design5) primary point of contact for assigned study sites6) tracking patient enrollment, study supplies, and reviewing data entry efforts of assigned study sites7) performing clinical data review for enrolled patients, query resolution and assessing data discrepancies within clinical databases8) resolving internal and external clinical issues for client research projects9) reporting of Serious Adverse Event (SAE) according to project specifications
  • University Hospital Heidelberg
    Clinical Scientist, Oncology (Post Doc)
    University Hospital Heidelberg Nov 2016 - Nov 2018
    Heidelberg, Baden-Württemberg, De
    Translational Oncology (lymphoma and leukemia).Establishment of the state of art microscopy based ex-vivo drug testing platform for patients with lymphoma (organotypic cultures of primary LN cells from lymphoma patient biopsies). ACHIEVMENTS:1) Development of 3D lymph node:- establishment of the unique biobanking procedure of lymph node lymphocytes and lymph node stromal cell isolated from patient lymph node biopsies, - co-culture of patient lymph node lymphocytes and stromal cells in 2D and 3D culture set-up- design of 3D culture material to meet the growth need of lymph node lymphocytes and lymph node stromal cells in one hydrogel drop - establishment of the confocal microscopy read out for viability of complex lymph node co-cultures under basal conditions and after drug treatment - drug testing on complex lymph node co-culture models- establishment of FACS panel to discriminate different cell types present in the lymph node stromal cell compartment2) SCSq of the lymph node lymphocytes: - establishment of the single cell transcriptome analysis (10x Genomics)3) Data analysis:- establishment of the quantitative analysis of the confocal microscopy pictures (z-stacks) in 3D volume in close collaboration with bioinformatic team at EMBL (advancement over maximal projection)Publication:Roider et al, Dissecting intratumour heterogeneity of nodal B-cell lymphomas at the transcriptional, genetic and drug-response levels, Nature Cell Biology, Jan2020
  • Erasmus Mc
    Scientist In Translational Research, Lung Diseases (Phd )
    Erasmus Mc 2011 - May 2016
    Rotterdam, Zuid-Holland, Nl
    Studies on Airway inflammation and remodeling in Chronic Lung Diseases (in patient-based advanced airway models): The EGFR-ADAM17 axis controls inflammatory responses in Cystic Fibrosis and Chronic Obstructive Pulmonary Disease. Publications:2018, Stolarczyk et al, The EGFR-ADAM17 Axis in Chronic Obstructive Pulmonary Disease and Cystic Fibrosis Lung Pathology, Mediators Inflame 2018, Stolarczyk et al, Extracellular oxidation in cystic fibrosis airway epithelium causes enhanced EGFR/ADAM17 activity, Am J Physiol Lung Cell Mol Physiol.2016 Stolarczyk et al., ADAM17 and EGFR regulate IL-6 receptor and amphiregulin in COPD bronchial epithelial cells, Physiol Rep2016, Veltman et al., Correction of Lung Inflammation in a F508del CFTR murine Cystic Fibrosis model by the Sphingosine-1-Phosphate Lyase Inhibitor LX2931, Am J Physiol Lung Cell Mol Physiol2014, Palomo, et al., Role of IL-1β in experimental cystic fibrosis upon P.aeruginosa infection, PLoS One
  • Mcgill University
    Fellowship At Mcgill University (Prestigeous Embo Award).
    Mcgill University Jan 2015 - Jul 2015
    Montreal, Qc, Ca
    Fellowship for a project awarded by EMBO: the role of ADAM17 and EGFR in Cystic Fibrosis. It ended up with scientific publication:2018, Stolarczyk et al, Extracellular oxidation in cystic fibrosis airway epithelium causes enhanced EGFR/ADAM17 activity, Am J Physiol Lung Cell Mol Physiol.
  • Adamed Group
    Research Assistant (Ended With Msc)
    Adamed Group 2009 - 2010
    Warsaw, Poland, Pl
    Research assistance in pre-clinical studies concerning diabetes type 2 (ended with Master Degree). Review:Stolarczyk et al, Nuclear receptors PPAR as a drug target in metabolic disorders, Post Biochem
  • Novum
    Trainee In Ivf Clinic
    Novum 2009 - 2009
    Short intern in the in vitro fertilisation clinic.
  • Bioton S.A.
    Trainee
    Bioton S.A. 2009 - 2009
    Ożarów Mazowiecki, Mazowieckie, Pl

Dr. Marta Stolarczyk Skills

Molecular Biology Cell Biology Cell Culture Biochemistry Western Blotting Pcr Life Sciences Genetics Qpcr Biotechnology Cystic Fibrosis Lung

Dr. Marta Stolarczyk Education Details

  • Dkfz German Cancer Research Center
    Dkfz German Cancer Research Center
    Oncology And Cancer Biology
  • Erasmus University Rotterdam
    Erasmus University Rotterdam
    Lung Diseases: Copd And Cystic Fibrosis
  • Mcgill University
    Mcgill University
    Cystic Fibrosis
  • University Of Warsaw
    University Of Warsaw
    Diabetes And Other Metabolic Disorders
  • University Of Warsaw
    University Of Warsaw
    Biotechnology

Frequently Asked Questions about Dr. Marta Stolarczyk

What company does Dr. Marta Stolarczyk work for?

Dr. Marta Stolarczyk works for X4 Pharmaceuticals

What is Dr. Marta Stolarczyk's role at the current company?

Dr. Marta Stolarczyk's current role is Principal Medical Science Liaison covering EU (R and D - Medical Affairs - EU).

What is Dr. Marta Stolarczyk's email address?

Dr. Marta Stolarczyk's email address is st****@****ail.com

What schools did Dr. Marta Stolarczyk attend?

Dr. Marta Stolarczyk attended Dkfz German Cancer Research Center, Erasmus University Rotterdam, Mcgill University, University Of Warsaw, University Of Warsaw.

What skills is Dr. Marta Stolarczyk known for?

Dr. Marta Stolarczyk has skills like Molecular Biology, Cell Biology, Cell Culture, Biochemistry, Western Blotting, Pcr, Life Sciences, Genetics, Qpcr, Biotechnology, Cystic Fibrosis, Lung.

Who are Dr. Marta Stolarczyk's colleagues?

Dr. Marta Stolarczyk's colleagues are Amy Musick, Sonia G., Javaria Suhail, Sondra Devorss, Halenya Monticelli, Steve Mussoline, Stephani Keetch.

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