Kurzvorstellung

• Leading and directing state-of-the-art drug safety studies
• Design, planning and execution of biological experiments
• Development of various cell-based and immunological assays

Ich biete

  • Biologie
  • Hardware Entwicklung

Projekt‐ & Berufserfahrung

study director/Project leader
Philip Morris, Neuchatel
7/2012 – 3/2015 (2 Jahre, 9 Monate)
Life Sciences
Tätigkeitszeitraum

7/2012 – 3/2015

Tätigkeitsbeschreibung

 Directing and leading of projects including scheduling, planning, design, execution and data analysis.
 Directing and leading of cross-functional study team (technicians and scientists).
 Preparation of project plans and set up of study objectives, tasks, milestones, time lines, budget planning, etc.
 Project meetings attendance, assessment of project risks, take minutes and keep track of actions.
 Lead project kick-off and closure meetings
 Analysis, interpretation, troubleshooting, presentation and reporting of the obtained results.
 Writing and reviewing of scientific documents – publications, abstracts, posters, study plans, study reports, business cases, SOPs, Wikis and study proposals.
 Literature research/review and interpretation of scientific data
 Presentations on congresses, meetings and steering committees.
 Establish strategy for the development of new projects and assays.
 Lead projects with multiple external stakeholders including contractors, research partners, product vendors, manufacturing facilities, etc.

Eingesetzte Qualifikationen

Windows XP

Zertifikate

PhD diploma in Biochemistry
Februar 2005

Ausbildung

PhD in Biochemistry
(Ausbildung)
Jahr: 2005
Ort: Bern, Switzerland

Qualifikationen

• Leading and directing state-of-the-art drug safety studies
• Managing of cross-functional study teams in a matrix organization
• Project management
• Design, planning and execution of biological experiments
• Development of various cell-based immunoassays and bioanalytical methods
• Development of advanced in vitro 3D organotypic tissue cultures (oral – buccal and gingival, bronchial, nasal and liver) for assessment of drug-induced toxicity
• Extensive experience in molecular and cell biology techniques
• Analysis, evaluation, interpretation, troubleshooting, presentation and reporting of the obtained results
• Writing of technical documents such as study plans, study reports, SOPs, study proposals, brochures, study overviews, etc
• Writing, review and editing of scientific manuscripts, abstracts, posters, letters, etc.
• Strong knowledge in various therapeutic areas – inflammation, diabetes and liver diseases
• Scientific presentations on congresses, meetings and steering committees
• Systematic literature research/review and interpretation of scientific data

Über mich

Highly motivated accomplished scientist with extensive research experience in pre-clinical mechanistic drug safety, various therapeutic areas, molecular and cell biology in both pharmaceutical industry and academy environment. Demonstrated leadership strengths and proven ability to successfully lead multiple projects from idea generation to launch and manage study teams in a fast-paced international industry environment with critical deadlines. Strong analytical thinker with excellent communication, organization, presentation and problem-solving skills. Strong team player with independent working style and ability to deliver efficiently results to meet tight time lines.

Persönliche Daten

Sprache
  • Bulgarisch (Muttersprache)
Reisebereitschaft
auf Anfrage
Arbeitserlaubnis
  • Europäische Union
  • Schweiz
Profilaufrufe
841
Alter
47
Berufserfahrung
20 Jahre und 7 Monate (seit 07/2000)
Projektleitung
6 Jahre

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